Patent Application
20150299313
The present application claims the priority based on Japanese Patent Application Nos. 2011-221400 (filed on Oct. 5, 2011), the contents of which are incorporated herein by reference in their entirety.
The present invention relates to an antigen-binding molecule for promoting uptake of an antigen into a cell, an antigen-binding molecule capable of promoting a decrease of the antigen concentration in plasma, an antigen-binding molecule capable of binding to an antigen a plurality of times, an antigen-binding molecule improved in pharmacokinetics, a pharmaceutical composition containing such an antigen-binding molecule and a method for producing the same.
Antibodies have received attention as pharmaceutical agents because of their high stability in plasma and few adverse reactions. Among others, many IgG antibody drugs have already been launched, and a large number of antibody drugs are still under development (Non Patent Literatures 1 and 2). Meanwhile, various techniques applicable to second-generation antibody drugs have been developed. For example, techniques of improving effector functions, antigen-binding ability, pharmacokinetics, or stability or of reducing the risk of immunogenicity have been reported (Non Patent Literature 3). Possible problems of such antibody drugs are the difficult preparation of subcutaneous administration preparations (this is because the antibody drugs are generally administered at very high doses), high production cost, etc. Methods for improving the pharmacokinetics of antibodies and methods for improving the affinity of antibodies for their antigens may be used for reducing the doses of the antibody drugs.
The artificial substitution of amino acids in constant regions has been reported as a method for improving the pharmacokinetics of antibodies (Non Patent Literatures 4 and 5). Previously reported affinity maturation, a technique of enhancing antigen-binding ability and antigen-neutralizing ability (Non Patent Literature 6), involves mutating amino acids in, for example, CDR regions of variable regions, to thereby achieve enhanced antigen-binding activity. Such enhancement in antigen-binding ability can improve biological activity in vitro or reduce doses and can further improve drug efficacy in vivo (Non Patent Literature 7).
The amount of an antigen that can be neutralized by one antibody molecule depends on affinity. Stronger affinity allows the antibody in a smaller amount to neutralize the antigen. The antibody affinity can be enhanced by various methods (Non Patent Literature 6). An antibody capable of covalently binding to an antigen with infinite affinity would be able to neutralize, by one molecule, one antigen molecule (or two antigens in the case of a divalent antibody). Previous methods, however, have a stoichiometric limitation of neutralization reaction up to one antigen molecule (or two antigens in the case of a divalent antibody) per antibody molecule and are unable to completely neutralize an antigen using an antibody in an amount below the amount of the antigen. In short, these methods have the limited effect of enhancing affinity (Non Patent Literature 9). A given duration of the neutralizing effect of a neutralizing antibody requires administering the antibody in an amount above the amount of an antigen produced in vivo for the period. Only the above-mentioned technique for improvement in the pharmacokinetics of antibodies or affinity maturation is not sufficient for reducing the necessary antibody doses. In this respect, one antibody must neutralize a plurality of antigens in order to sustain its antigen-neutralizing effect for the period of interest in an amount below the amount of the antigen. In order to attain this object, an antibody binding to an antigen in a pH-dependent manner has been reported recently as a novel approach (Patent Literature 1). This pH-dependent antigen-binding antibody is strongly associated with an antigen under the neutral condition in plasma and dissociated from the antigen under the acidic condition in endosome. Thus, the pH-dependent antigen-binding antibody can be dissociated from the antigen in endosome. The pH-dependent antigen-binding antibody thus dissociated from the antigen can be reassociated with an antigen after being recycled into plasma by FcRn. This allows one antibody to bind to a plurality of antigens repeatedly.
Retentivity of an antigen in plasma is extremely short, compared to an antibody, which binds to FcRn and is repeatedly used. When such an antibody having long plasma retentivity binds to an antigen thereof, the retentivity of an antibody-antigen complex in plasma becomes long like the antibody. Therefore, an antigen acquires long plasma retentivity by binding to an antibody, with the result that the concentration of the antigen in plasma increases. In this case, even if the affinity of an antibody for an antigen is improved, clearance of the antigen from plasma cannot be promoted. The aforementioned pH-dependent antigen-binding antibody is reported to be effective as a method for promoting clearance of an antigen from plasma compared to general antibodies (Patent Literature 1).
As described above, the pH-dependent antigen-binding antibody solely binds to a plurality of antigen molecules and thus can promote clearance of the antigen molecules from plasma, compared to general antibodies. Therefore, the pH-dependent antigen-binding antibody has a function that cannot be attained by general antibodies. However, up until now, antibody-engineering techniques for further improving an effect of a pH-dependent antigen-binding antibody in repeatedly binding to an antigen and an effect of an antibody in promoting clearance of an antigen from plasma have not yet been reported.
In the meantime, a glycoprotein present in plasma binds to a sugar chain specific receptor and disappears from the plasma (Non Patent Literature 10). At this time, the glycoprotein binds to a sugar chain receptor present in a cell surface and is taken up into a cell. In the cell, the glycoprotein is dissociated from the sugar chain receptor and decomposed by lysosome; whereas, the sugar chain receptor is known to return to the cell surface for recycle use. More specifically, a glycoprotein and a sugar chain receptor strongly bind under a neutral condition in plasma and dissociate under an acidic condition within an endosome. In short, the sugar chain receptor has a pH-dependent binding ability (Non Patent Literature 11, Non Patent Literature 12). In such pH-dependent binding between a glycoprotein and a sugar chain receptor, a sugar chain added to the glycoprotein is involved. Examples of such combination of a sugar chain and a sugar chain receptor include a combination of a sugar chain such as N-linked sugar chain having galactose at a terminal and an asialoglycoprotein receptor (Non Patent Literature 11); and a combination of a sugar chain having mannose at a terminal and a mannose receptor (Non Patent Literature 12).
From the properties of such an N-linked sugar chain, it has been considered unfavorable to add an N-linked sugar chain, which is not functionally required for a biotechnology-based pharmaceutical product containing an antibody, in view of maintaining its efficacy or retentivity in plasma (Non Patent Literature 13, 14). Such an N-linked sugar chain has not yet been actually used in practice for further improving an effect of promoting clearance of an antigen from plasma.
Reference documents cited in the specification are as follows. The contents described in these documents are all incorporated herein by reference. However, these documents are not always admitted to correspond to prior art documents to the specification of the present application.
The present inventors conducted intensive studies on a method for promoting uptake of an antigen into a cell by an antigen-binding molecule having an antigen-binding activity; a method for allowing an antigen-binding molecule to bind to an antigen a plurality of times; a method for promoting a decrease of an antigen concentration in plasma by administering an antigen-binding molecule; and a method for improving retentivity of an antigen-binding molecule in plasma. As a result, the present inventors found that an antigen-binding molecule, which has an antigen-binding domain, a binding domain to FcRn (particularly human FcRn) and a domain binding to a sugar chain receptor, and which has a weak binding ability (binding to a sugar-chain receptor) in the ion-concentration condition of an endosome compared to the ion-concentration condition of plasma, can promote uptake of an antigen into a cell; that an antigen-binding molecule having an antigen-binding domain, whose antigen-binding activity in the ion-concentration condition of early-stage endosome is weak compared to the antigen-binding activity of the ion-concentration condition in plasma, can further promote uptake of an antigen into a cell by the antigen-binding molecule; that the number of antigens, to which a single antigen-binding molecule can bind, can be increased; that a decrease of the antigen concentration in plasma is promoted by administering an antigen-binding molecule; and that pharmacokinetics of an antigen-binding molecule can be improved.
More specifically, the present invention relates to a method for promoting uptake of an antigen into a cell by an antigen-binding molecule; a method for increasing the number of antigens to which a single antigen-binding molecule can bind; a method for promoting a decrease of the antigen concentration in plasma by administration of the antigen-binding molecule; a method for improving the pharmacokinetics of an antigen-binding molecule; an antigen-binding molecule promoting uptake of an antigen into a cell; an antigen-binding molecule capable of binding a larger number of antigens; an antigen-binding molecule capable of promoting a decrease of the antigen concentration in plasma by administration of the antigen-binding molecule; an antigen-binding molecule improved in pharmacokinetics; a pharmaceutical composition containing such an antigen-binding molecule; and a method for producing the same. More specifically, the present invention provides:
[1] A method for producing an antigen-binding molecule, including the following steps:
(a) a step of providing a polypeptide sequence of an antigen-binding molecule containing an antigen-binding domain and an FcRn binding domain,
(b) a step of identifying an amino acid sequence serving as a candidate for a motif for a sugar chain receptor-binding domain in the polypeptide sequence,
(c) a step of designing the motif for a sugar chain receptor-binding domain containing an amino acid sequence having at least one amino acid different from the amino acid sequence identified in the step (b),
(d) a step of preparing a gene encoding a polypeptide of an antigen-binding molecule containing the motif for the sugar chain receptor-binding domain designed in the step (c), and
(e) a step of recovering the antigen-binding molecule from a culture fluid of a host cell transformed with the gene obtained in the step (d).
[2] The method according to [1], further including a step of treating the antigen-binding molecule obtained in the step (e) with an enzyme.
[3] The method according to [1] or [2], in which a binding activity of the antigen-binding domain to an antigen changes depending upon an ion-concentration condition.
[4] The method according to [3], in which the ion-concentration condition is a pH condition.
[5] The method according to [4], in which the antigen-binding domain has a higher binding activity to an antigen under a neutral pH range condition than a binding activity to the antigen under an acidic pH range condition.
[6] The method according to [5], in which the antigen-binding domain having a higher binding activity to the antigen under a neutral pH range condition than a binding activity to the antigen under an acidic pH range condition is provided by substituting at least one amino acid of the antigen-binding domain with an amino acid whose side chain has a pKa of 4.0-8.0 or by inserting at least one amino acid whose side chain has a pKa of 4.0-8.0 into the antigen-binding domain.
[7] The method according to [3], in which the ion-concentration condition is a calcium-ion concentration condition.
[8] The method according to [7], in which the antigen-binding domain has a higher binding activity to the antigen under a high calcium-ion concentration condition than a binding activity to the antigen under a low calcium-ion concentration condition.
[9] The method according to [8], in which the antigen-binding domain having a higher binding activity to the antigen under a high calcium-ion concentration condition than a binding activity to the antigen under a low calcium-ion concentration condition is provided by substituting at least one amino acid of the antigen-binding domain with a calcium-binding motif or by inserting a calcium-binding motif into the antigen-binding domain.
[10] The method according to any one of [1] to [9], in which the antigen-binding domain contains a variable region of an antibody.
[11] The method according to any one of [1] to [10], in which the FcRn binding domain contains an Fc region of an antibody.
[12] The method according to [11], in which the antibody is an IgG antibody.
[13] The method according to [12], in which the IgG antibody is IgG1, IgG2, IgG3 or IgG4.
[14] The method according to any one of [1] to [12], in which the binding activity of the sugar chain receptor-binding domain to a sugar chain receptor changes depending upon an ion-concentration condition.
[15] The method according to [14], in which the ion-concentration condition is a pH condition.
[16] The method according to any one of [1] to [15], in which a binding activity of the sugar chain receptor-binding domain to the sugar chain receptor under a neutral pH range condition is higher than a binding activity to the sugar chain receptor under an acidic pH range condition.
[17] The method according to [14], in which the ion-concentration condition is a calcium-ion concentration condition.
[18] The method according to [17], in which a binding activity of the sugar chain receptor-binding domain to the sugar chain receptor under a high calcium-ion concentration condition is higher than a binding activity to the sugar chain receptor under a low calcium-ion concentration condition.
[19] The method according to any one of [1] to [18], in which the sugar chain receptor-binding domain is a sugar chain.
[20] The method according to [19], in which the sugar chain is an O-linked sugar chain.
[21] The method according to [19], in which the sugar chain is an N-linked sugar chain.
[22] The method according to [21], in which designing a motif for the sugar chain receptor-binding domain include designing a motif to which an N-linked sugar chain is added.
[23] The method according to [21] or [22], in which a terminal of the N-linked sugar chain contains galactose.
[24] The method according to [23], in which a terminal of the N-linked sugar chain contains three or more galactoses.
[25] The method according to any one of [21] to [24], in which the sugar chain receptor is an asialoglycoprotein receptor.
[26] The method according to [21] or [22], in which a terminal of the N-linked sugar chain contains mannose.
[27] The method according to [26], in which the sugar chain receptor is a mannose receptor.
[28] An antigen-binding molecule prepared by the method according to any one of [1] to [27].
[29] An antigen-binding molecule containing an FcRn binding domain, an antigen-binding domain whose binding activity to an antigen changes depending upon an ion-concentration condition, and one or more sugar chain receptor-binding domains whose binding activity to a sugar chain receptor changes depending upon an ion-concentration condition.
[30] The antigen-binding molecule according to [29], in which a binding activity of the antigen-binding domain to the antigen changes depending upon a pH condition.
[31] The antigen-binding molecule according to [30], in which a binding activity of the antigen-binding domain to the antigen under a neutral pH range condition is higher than a binding activity to the antigen under an acidic pH range condition.
[32] The antigen-binding molecule according to [31], in which at least one amino acid of the antigen-binding domain includes at least one amino acid whose side chain has a pKa of 4.0-8.0.
[33] The antigen-binding molecule according to [29], in which a binding activity of the antigen-binding domain to the antigen changes depending upon the calcium-ion concentration condition.
[34] The antigen-binding molecule according to [33], in which a binding activity of the antigen-binding domain to the antigen under a high calcium-ion concentration condition is higher than a binding activity to the antigen under a low calcium-ion concentration condition.
[35] The antigen-binding molecule according to [34], in which at least one amino acid of the antigen-binding domain includes a calcium-binding motif.
[36] The antigen-binding molecule according to any one of [29] to [35] in which the antigen-binding domain contains a variable region of an antibody.
[37] The antigen-binding molecule according to any one of [29] to [36], in which the FcRn binding domain contains an Fc region of an antibody.
[38] The antigen-binding molecule according to [37], in which the antibody is an IgG antibody.
[39] The antigen-binding molecule according to [38], in which the IgG antibody is IgG1, IgG2, IgG3 or IgG4.
[40] The antigen-binding molecule according to any one of [29] to [39], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor changes depending upon an ion-concentration condition.
[41] The antigen-binding molecule according to [40], in which the ion-concentration condition is a pH condition.
[42] The antigen-binding molecule according to [41], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor under a neutral pH range condition is higher than a binding activity to the sugar chain receptor under an acidic pH range condition.
[43] The antigen-binding molecule according to [40], in which the ion-concentration condition is the calcium-ion concentration condition.
[44] The antigen-binding molecule according to [43], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor under a high calcium-ion concentration condition is higher than a binding activity to the sugar chain receptor under a low calcium-ion concentration condition.
[45] The antigen-binding molecule according to any one of [29] to [44], in which the sugar chain receptor-binding domain is a sugar chain.
[46] The antigen-binding molecule according to [45], in which the sugar chain is an O-linked sugar chain or an N-linked sugar chain.
[47] The antigen-binding molecule according to [46], in which the sugar chain receptor-binding domain includes a motif to which an N-linked sugar chain is bound.
[48] The antigen-binding molecule according to [46] or [47], in which a terminal of the N-linked sugar chain contains galactose.
[49] The antigen-binding molecule according to [48], in which a terminal of the N-linked sugar chain contains c.
[50] The antigen-binding molecule according to any one of [47] to [49], in which the sugar chain receptor is an asialoglycoprotein receptor.
[51] The antigen-binding molecule according to [46] or [47], in which a terminal of the N-linked sugar chain contains mannose.
[52] The antigen-binding molecule according to [46] or [47], in which the sugar chain receptor is a mannose receptor.
[53] The antigen-binding molecule according to any one of [28] to [52], in which the antigen-binding molecule is an antibody.
[54] The antigen-binding molecule according to any one of [28] to [53], in which the sugar chain receptor-binding domain is contained in the antigen-binding domain.
[55] The antigen-binding molecule according to any one of [28] to [53], in which the sugar chain receptor-binding domain is contained in the FcRn binding domain.
[56] A pharmaceutical composition containing an antigen-binding molecule according to any one of [28] to [55].
[57] A method for allowing a cell expressing a sugar chain receptor to take up an antigen-binding molecule according to any one of [28] to [55] in to the cell, comprising bringing the antigen-binding molecule into contact with the cell in-vivo or ex-vivo.
[58] A method for allowing a cell expressing a sugar chain receptor to take up an antigen bound to an antigen-binding molecule according to any one of [28] to [55], comprising bringing the antigen-binding molecule into contact with the cell in-vivo or ex-vivo.
[59] A method for increasing the number of antigens to which a single antigen-binding molecule according to any one of [28] to [55] binds, comprising bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor, in-vivo or ex-vivo.
[60] A method for decreasing the number of an antigen being present in an extracellular space, comprising bringing an antigen-binding molecule according to any one of [28] to [55] into contact with a cell expressing a sugar chain receptor, in-vivo or ex-vivo.
[61] The method according to [58], in which the extracellular space is plasma.
[62] A method for improving the pharmacokinetics of an antigen-binding molecule according to any one of [28] to
[55], comprising bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor, in-vivo.
[63] A method for promoting dissociation of an antigen bound extracellularly to an antigen-binding molecule according to any one of [28] to [55] from the antigen-binding molecule, comprising bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor, in-vivo or ex-vivo.
[64] A method selected from the following methods:
(i) a method for promoting uptake of an antigen-binding molecule into a cell expressing the sugar chain receptor, in-vivo or ex-vivo;
(ii) a method for promoting uptake of an antigen bound to an antigen-binding molecule into a cell expressing a sugar chain receptor, in-vivo or ex-vivo;
(iii) a method for increasing the number of an antigen to which a single antigen-binding molecule binds, in-vivo or ex-vivo;
(iv) a method for enhancing potency of an antigen-binding molecule to clear an antigen, in-vivo or ex-vivo;
(v) a method for improving the pharmacokinetics of an antigen-binding molecule; or
(vi) a method for promoting dissociation of an antigen which has bound extracellularly to an antigen-binding molecule;
the method comprising, in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and one or more binding domains to a sugar chain receptor, increasing the number of the binding domains to the sugar chain receptor.
[65] The method according to [64], in which a binding activity of the antigen-binding molecule to an antigen changes depending upon an ion-concentration condition.
[66] The method according to [64], in which a binding activity of the antigen-binding domain to an antigen changes depending upon a pH condition.
[67] The method according to [66], in which a binding activity of the antigen-binding domain to an antigen under a neutral pH range condition is higher than a binding activity to the antigen under an acidic pH range condition.
[68] The method according to [67], in which at least one amino acid of the antigen-binding domain includes at least one amino acid whose side chain has a pKa of 4.0-8.0.
[69] The method according to [64], in which a binding activity of the antigen-binding domain to an antigen changes depending upon a calcium-ion concentration condition.
[70] The method according to [69], in which a binding activity of the antigen-binding domain to an antigen under a high calcium-ion concentration condition is higher than a binding activity to the antigen under a low calcium-ion concentration condition.
[71] The method according to [70], in which at least one amino acid of the antigen-binding domain includes a calcium-binding motif.
[72] The method according to any one of [64] to [71], in which the antigen-binding domain contains a variable region of an antibody.
[73] The method according to any one of [64] to [72], in which the FcRn binding domain contains an Fc region of an antibody.
[74] The method according to [73], in which the antibody is an IgG antibody.
[75] The method according to [74], in which the IgG antibody is IgG1, IgG2, IgG3 or IgG4.
[76] The method according to any one of [64] to [75], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor changes depending upon an ion-concentration condition.
[77] The method according to [76], in which the ion-concentration condition is a pH condition.
[78] The method according to [76], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor under a neutral pH range condition is higher than a binding activity to the sugar chain receptor under an acidic pH range condition.
[79] The method according to [76], in which the ion-concentration condition is a calcium-ion concentration condition.
[80] The method according to [79], in which a binding activity of the sugar chain receptor-binding domain to a sugar chain receptor under a high calcium-ion concentration condition is higher than a binding activity to the sugar chain receptor under a low calcium-ion concentration condition.
[81] The method according to any one of [64] to [80], in which the sugar chain receptor-binding domain is a sugar chain.
[82] The method according to [81], in which the sugar chain is an O-linked sugar chain.
[83] The method according to [81], in which the sugar chain is an N-linked sugar chain.
[84] The method according to [83], in which the sugar chain receptor-binding domain contains a motif to which an N-linked sugar chain is bound.
[85] The method according to [83] or [84], in which a terminal of the N-linked sugar chain contains galactose.
[86] The method according to [85], in which a terminal of the N-linked sugar chain contains three or more terminal galactoses.
[87] The method according to any one of [84] to [86], in which the sugar chain receptor is an asialoglycoprotein receptor.
[88] The method according to [83] or [84], in which a terminal of the N-linked sugar chain contains mannose.
[89] The method according to [83] or [84], in which the sugar chain receptor is a mannose receptor.
[90] The method according to any one of [64] to [89], in which the antigen-binding molecule is an antibody.
[91] The method according to any one of [64] to [90], in which the sugar chain receptor-binding domain is contained in the antigen-binding domain.
[92] The method according to any one of [64] to [90], in which the sugar chain receptor-binding domain is contained in the FcRn binding domain.
The following definitions and detailed descriptions are provided to promote understanding of the present invention described in the specification.
Each amino acid is indicated herein by single-letter code or three-letter code, or both, as represented by, for example, Ala/A, Leu/L, Arg/R, Lys/K, Asn/N, Met/M, Asp/D, Phe/F, Cys/C, Pro/P, Gln/Q, Ser/S, Glu/E, Thr/T, Gly/G, Trp/W, His/H, Tyr/Y, Ile/I, and Val/V.
The term “and/or” described herein is meant to include every combination appropriately represented by “and” and “or”. Specifically, for example, the phrase “amino acids 33, 55, and/or 96 are substituted” includes the following variations of amino acid modification: (a) position 33, (b) position 55, (c) position 96, (d) positions 33 and 55, (e) positions 33 and 96, (f) positions 55 and 96, and (g) positions 33, 55, and 96.
The “antigen” described herein is not limited by a particular structure as long as the antigen comprises an epitope to which the antigen-binding domain binds. In another sense, the antigen may be inorganic matter or may be organic matter. As the antigen-binding molecule improved in pharmacokinetics by the method of the present invention, antigen-binding molecules recognizing a membrane antigen such as receptor proteins (membrane bound receptor, soluble receptor) and cell surface markers, and antigen-binding molecules recognizing a soluble antigen such as cytokines are preferably mentioned. Examples of the antigen can include the following molecules: 17-IA, 4-1BB, 4Dc, 6-keto-PGF1a, 8-iso-PGF2a, 8-oxo-dG, A1 adenosine receptor, A33, ACE, ACE-2, activin, activin A, activin AB, activin B, activin C, activin RIA, activin RIA ALK-2, activin RIB ALK-4, activin RIIA, activin RIIB, ADAM, ADAM10, ADAM12, ADAM15, ADAM17/TACE, ADAM8, ADAMS, ADAMTS, ADAMTS4, ADAMTS5, addressin, aFGF, ALCAM, ALK, ALK-1, ALK-7, alpha-1-antitrypsin, alpha-V/beta-1 antagonist, ANG, Ang, APAF-1, APE, APJ, APP, APRIL, AR, ARC, ART, artemin, anti-Id, ASPARTIC, atrial natriuretic factor, av/b3 integrin, Axl, b2M, B7-1, B7-2, B7-H, B-lymphocyte stimulator (BlyS), BACE, BACE-1, Bad, BAFF, BAFF-R, Bag-1, BAK, Bax, BCA-1, BCAM, Bcl, BCMA, BDNF, b-ECGF, bFGF, BID, Bik, BIM, BLC, BL-CAM, BLK, BMP, BMP-2 BMP-2a, BMP-3 osteogenin, BMP-4 BMP-2b, BMP-5, BMP-6 Vgr-1, BMP-7 (OP-1), BMP-8 (BMP-8a, OP-2), BMPR, BMPR-IA (ALK-3), BMPR-IB (ALK-6), BRK-2, RPK-1, BMPR-II (BRK-3), BMP, b-NGF, BOK, bombesin, bone-derived neurotrophic factor, BPDE, BPDE-DNA, BTC, complement factor 3 (C3), C3a, C4, C5, C5a, C10, CA125, CAD-8, calcitonin, cAMP, carcinoembryonic antigen (CEA), cancer-associated antigens, cathepsin A, cathepsin B, cathepsin C/DPPI, cathepsin D, cathepsin E, cathepsin H, cathepsin L, cathepsin 0, cathepsin S, cathepsin V, cathepsin X/Z/P, CBL, CCI, CCK2, CCL, CCL1, CCL11, CCL12, CCL13, CCL14, CCL15, CCL16, CCL17, CCL18, CCL19, CCL2, CCL20, CCL21, CCL22, CCL23, CCL24, CCL25, CCL26, CCL27, CCL28, CCL3, CCL4, CCL5, CCL6, CCL7, CCL8, CCL9/10, CCR, CCR1, CCR10, CCR10, CCR2, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8, CCR9, CD1, CD2, CD3, CD3E, CD4, CD5, CD6, CD7, CD8, CD10, CD11a, CD11b, CD11c, CD13, CD14, CD15, CD16, CD18, CD19, CD20, CD21, CD22, CD23, CD25, CD27L, CD28, CD29, CD30, CD30L, CD32, CD33 (p67 protein), CD34, CD38, CD40, CD40L, CD44, CD45, CD46, CD49a, CD52, CD54, CD55, CD56, CD61, CD64, CD66e, CD74, CD80 (B7-1), CD89, CD95, CD123, CD137, CD138, CD140a, CD146, CD147, CD148, CD152, CD164, CEACAM5, CFTR, cGMP, CINC, botulinum toxin, Clostridium perfringens toxin, CKb8-1, CLC, CMV, CMV UL, CNTF, CNTN-1, COX, C-Ret, CRG-2, CT-1, CTACK, CTGF, CTLA-4, CX3CL1, CX3CR1, CXCL, CXCL1, CXCL2, CXCL3, CXCL4, CXCL5, CXCL6, CXCL7, CXCL8, CXCL9, CXCL10, CXCL11, CXCL12, CXCL13, CXCL14, CXCL15, CXCL16, CXCR, CXCR1, CXCR2, CXCR3, CXCR4, CXCR5, CXCR6, cytokeratin tumor-associated antigens, DAN, DCC, DcR3, DC-SIGN, decay accelerating factor, des(1-3)-IGF-I (brain IGF-1), Dhh, digoxin, DNAM-1, Dnase, Dpp, DPPIV/CD26, Dtk, EGAD, EDA, EDA-A1, EDA-A2, EDAR, EGF, EGFR (ErbB-1), EMA, EMMPRIN, ENA, endothelin receptor, enkephalinase, eNOS, Eot, eotaxin 1, EpCAM, ephrin B2/EphB4, EPO, ERCC, E-selectin, ET-1, factor IIa, factor VII, factor VIIIc, factor IX, fibroblast-activating protein (FAP), Fas, FcR1, FEN-1, ferritin, FGF, FGF-19, FGF-2, FGF3, FGF-8, FGFR, FGFR-3, fibrin, FL, FLIP, Flt-3, Flt-4, follicle-stimulating hormone, fractalkine, FZD1, FZD2, FZD3, FZD4, FZD5, FZD6, FZD7, FZD8, FZD9, FZD10, G250, Gas6, GCP-2, GCSF, GD2, GD3, GDF, GDF-1, GDF-3 (Vgr-2), GDF-5 (BMP-14, CDMP-1), GDF-6 (BMP-13, CDMP-2), GDF-7 (BMP-12, CDMP-3), GDF-8 (myostatin), GDF-9, GDF-15 (MIC-1), GDNF, GDNF, GFAP, GFRa-1, GFR-alpha 1, GFR-alpha 2, GFR-alpha 3, GITR, glucagon, Glut4, glycoprotein IIb/IIIa (GPIIb/IIIa), GM-CSF, gp130, gp72, GRO, growth hormone-releasing factor, hapten (NP-cap or NIP-cap), HB-EGF, HCC, HCMV gB envelope glycoprotein, HCMV gH envelope glycoprotein, HCMVUL, hematopoietic growth factor (HGF), Hep B gp120, heparanase, Her2, Her2/neu (ErbB-2), Her3 (ErbB-3), Her4 (ErbB-4), herpes simplex virus (HSV) gB glycoprotein, HSV gD glycoprotein, HGFA, high-molecular-weight melanoma-associated antigen (HMW-MAA), HIV gp120, HIV IIIB gp 120 V3 loop, HLA, HLA-DR, HM1.24, HMFG PEM, HRG, Hrk, human heart myosin, human cytomegalovirus (HCMV), human growth hormone (HGH), HVEM, 1-309, IAP, ICAM, ICAM-1, ICAM-3, ICE, ICOS, IFNg, Ig, IgA receptor, IgE, IGF, IGF-binding protein, IGF-1R, IGFBP, IGF-I, IGF-II, IL, IL-1, IL-1R, IL-2, IL-2R, IL-4, IL-4R, IL-5, IL-5R, IL-6, IL-6R, IL-8, IL-9, IL-10, IL-12, IL-13, IL-15, IL-18, IL-18R, IL-23, interferon (INF)-alpha, INF-beta, INF-gamma, inhibin, iNOS, insulin chain A, insulin chain B, insulin-like growth factor 1, integrin alpha 2, integrin alpha 3, integrin alpha 4, integrin alpha 4/beta 1, integrin alpha 4/beta 7, integrin alpha 5 (alpha V), integrin alpha 5/beta 1, integrin alpha 5/beta 3, integrin alpha 6, integrin beta 1, integrin beta 2, interferon gamma, IP-10, I-TAC, JE, kallikrein 2, kallikrein 5, kallikrein 6, kallikrein 11, kallikrein 12, kallikrein 14, kallikrein 15, kallikrein L1, kallikrein L2, kallikrein L3, kallikrein L4, KC, KDR, keratinocyte growth factor (KGF), laminin 5, LAMP, LAP, LAP (TGF-1), latent TGF-1, latent TGF-1 bpi, LBP, LDGF, LECT2, lefty, Lewis-Y antigen, Lewis-Y-related antigen, LFA-1, LFA-3, Lfo, LIF, LIGHT, lipoprotein, LIX, LKN, Lptn, L-selectin, LT-a, LT-b, LTB4, LTBP-1, lung surface, luteinizing hormone, lymphotoxin beta receptor, Mac-1, MAdCAM, MAG, MAP2, MARC, MCAM, MCAM, MCK-2, MCP, M-CSF, MDC, Mer, metalloproteases, MGDF receptor, MGMT, MHC (HLA-DR), MIF, MIG, MIP, MIP-1-alpha, MK, MMAC1, MMP, MMP-1, MMP-10, MMP-11, MMP-12, MMP-13, MMP-14, MMP-15, MMP-2, MMP-24, MMP-3, MMP-7, MMP-8, MMP-9, MPIF, Mpo, MSK, MSP, mucin (Muc1), MUC18, mullerian-inhibiting substance, Mug, MuSK, NAIP, NAP, NCAD, N-C adherin, NCA 90, NCAM, NCAM, neprilysin, neurotrophin-3, -4, or -6, neurturin, nerve growth factor (NGF), NGFR, NGF-beta, nNOS, NO, NOS, Npn, NRG-3, NT, NTN, OB, OGG1, OPG, OPN, OSM, OX40L, OX40R, p150, p95, PADPr, parathyroid hormone, PARC, PARP, PBR, PBSF, PCAD, P-cadherin, PCNA, PDGF, PDGF, PDK-1, PECAM, PEM, PF4, PGE, PGF, PGI2, PGD2, PIN, PLA2, placental alkaline phosphatase (PLAP), P1GF, PLP, PP14, proinsulin, prorelaxin, protein C, PS, PSA, PSCA, prostate-specific membrane antigen (PSMA), PTEN, PTHrp, Ptk, PTN, R51, RANK, RANKL, RANTES, RANTES, relaxin A chain, relaxin B chain, renin, respiratory syncytial virus (RSV) F, RSV Fgp, Ret, rheumatoid factor, RLIP76, RPA2, RSK, 5100, SCF/KL, SDF-1, SERINE, serum albumin, sFRP-3, Shh, SIGIRR, SK-1, SLAM, SLPI, SMAC, SMDF, SMOH, SOD, SPARC, Stat, STEAP, STEAP-II, TACE, TACI, TAG-72 (tumor-associated glycoprotein-72), IARC, TCA-3, T cell receptor (e.g., T cell receptor alpha/beta), TdT, TECK, TEM1, TEM5, TEM7, TEM8, TERT, testicular PLAP-like alkaline phosphatase, TfR, TGF, TGF-alpha, TGF-beta, TGF-beta Pan Specific, TGF-beta RI (ALK-5), TGF-beta RII, TGF-beta RIIb, TGF-beta RIII, TGF-beta 1, TGF-beta 2, TGF-beta 3, TGF-beta 4, TGF-beta 5, thrombin, thymus Ck-1, thyroid stimulating hormone, Tie, TIMP, TIQ, tissue factor, TMEFF2, Tmpo, TMPRSS2, TNF, TNF-alpha, TNF-alpha/beta, TNF-beta 2, TNFc, TNF-RI, TNF-RII, INFRSF10A (TRAIL R1 Apo-2, DR4), TNFRSF10B (TRAIL R2 DR5, KILLER, TRICK-2A, TRICK-B), INFRSF10C (TRAILR3 DcR1, LIT, TRID), TNFRSF10D (TRAIL R4 DcR2, TRUNDD), TNFRSF11A (RANK ODF R, TRANCE R), TNFRSF11B (OPG OCIF, TR1), TNFRSF12 (TWEAK RFN14), TNFRSF13B (TACI), TNFRSF13C (BAFF R), TNFRSF14 (HVEM ATAR, HveA, LIGHT R, TR2), TNFRSF16 (NGFRp75NTR), TNFRSF17 (BCMA), TNFRSF18 (GITR AITR), TNFRSF19 (TROY TAJ, TRADE), TNFRSF19L (RELT), TNFRSF1A (TNF RI CD120a, p55-60), TNFRSF1B (TNF RII CD120b, p75-80), TNFRSF26 (TNFRH3), TNFRSF3 (LTbR TNF RIII, TNFC R), TNFRSF4 (OX4OACT35, TXGP1 R), TNFRSF5 (CD40 p50), TNFRSF6 (Fas Apo-1, APT1, CD95), TNFRSF6B (DcR3 M68, TR6), TNFRSF7 (CD27), TNFRSF8 (CD30), TNFRSF9 (4-1BB CD137, ILA), TNFRSF21 (DR6), TNFRSF22 (DcTRAIL R2 TNFRH2), TNFRST23 (DcTRAIL R1 TNFRH1), TNFRSF25 (DR3 Apo-3, LARD, TR-3, TRAMP, WSL-1), TNFSF10 (TRAIL Apo-2 ligand, TL2), TNFSF11 (TRANCE/RANK ligand ODF, OPG ligand), TNFSF12 (TWEAK Apo-3 ligand, DR3 ligand), TNFSF13 (APRIL TALL2), TNFSF13B (BAFF BLYS, TALL1, THANK, TNFSF20), TNFSF14 (LIGHT HVEM ligand, LTg), TNFSF15 (TL1A/VEGI), TNFSF18 (GITR ligand AITR ligand, TL6), TNFSF1A (TNF-α Conectin, DIF, TNFSF2), TNFSF1B (TNF-b LTa, TNFSF1), TNFSF3 (LTb TNFC, p33), TNFSF4 (OX40 ligand gp34, TXGP1), TNFSF5 (CD40 ligand CD154, gp39, HIGM1, IMD3, TRAP), TNFSF6 (Fas ligand Apo-1 ligand, APT1 ligand), TNFSF7 (CD27 ligand CD70), TNFSF8 (CD30 ligand CD153), TNFSF9 (4-1BB ligand CD137 ligand), TP-1, t-PA, Tpo, TRAIL, TRAIL R, TRAIL-R1, TRAIL-R2, TRANCE, transferrin receptor, TRF, Trk, TROP-2, TSG, TSLP, tumor-associated antigen CA125, tumor-associated antigen-expressing Lewis-Y-related carbohydrate, TWEAK, TXB2, Ung, uPAR, uPAR-1, urokinase, VCAM, VCAM-1, VECAD, VE-cadherin, VE-cadherin-2, VEFGR-1 (flt-1), VEGF, VEGFR, VEGFR-3 (flt-4), VEGI, VIM, viral antigens, VLA, VLA-1, VLA-4, VNR integrin, von Willebrand factor, WIF-1, WNT1, WNT2, WNT2B/13, WNT3, WNT3A, WNT4, WNT5A, WNT5B, WNT6, WNT7A, WNT7B, WNT8A, WNT8B, WNT9A, WNT9A, WNT9B, WNT10A, WNT10B, WNT11, WNT16, XCL1, XCL2, XCR1, XCR1, XEDAR, XIAP, XPD, HMGB1, IgA, Aβ, CD81, CD97, CD98, DDR1, DKK1, EREG, Hsp90, IL-17/IL-17R, IL-20/IL-20R, oxidized LDL, PCSK9, prekallikrein, RON, TMEM16F, SOD1, chromogranin A, chromogranin B, tau, VAP1, high-molecular-weight kininogen, IL-31, IL-31R, Navi.i, Nav1.2, Nav1.3, Nav1.4, Nav1.5, Nav1.6, Nav1.7, Nav1.8, Nav1.9, EPCR, C1, C1q, C1r, C1s, C2, C2a, C2b, C3, C3a, C3b, C4, C4a, C4b, C5, C5a, C5b, C6, C7, C8, C9, factor B, factor D, factor H, properdin, sclerostin, fibrinogen, fibrin, prothrombin, thrombin, tissue factor, factor V, factor Va, factor VII, factor VIIa, factor VIII, factor VIIIa, factor IX, factor IXa, factor X, factor Xa, factor XI, factor XIa, factor XII, factor XIIa, factor XIII, factor XIIIa, TFPI, antithrombin III, EPCR, thrombomodulin, TAPI, tPA, plasminogen, plasmin, PAI-1, PAI-2, GPC3, syndecan-1, syndecan-2, syndecan-3, syndecan-4, LPA, S1P, acetylcholine receptor, AdipoR1, AdipoR2, ADP ribosyl cyclase-1, alpha-4/beta-7 integrin, alpha-5/beta-1 integrin, alpha-v/beta-6 integrin, alpha-v/beta-1 integrin, angiopoietin ligand-2, Angpt12, Anthrax, cadherin, carbonic anhydrase-IX, CD105, CD155, CD158a, CD37, CD49b, CD51, CD70, CD72, Claudin 18, Clostridium difficile toxin, CS1, delta-like protein ligand 4, DHICA oxidase, Dickkopf-1 ligand, dipeptidyl peptidase IV, EPOR, F protein of RSV, factor Ia, FasL, folate receptor alpha, glucagon receptor, glucagon-like peptide 1 receptor, glutamate carboxypeptidase II, GMCSFR, hepatitis C virus E2 glycoprotein, hepcidin, IL-17 receptor, IL-22 receptor, IL-23 receptor, IL-3 receptor, Kit tyrosine kinase, leucine rich alpha-2-glycoprotein 1 (LRG1), lysosphingolipid receptor, membrane glycoprotein OX2, mesothelin, MET, MICA, MUC-16, myelin associated glycoprotein, neuropilin-1, neuropilin-2, Nogo receptor, PLXNA1, PLXNA2, PLXNA3, PLXNA4A, PLXNA4B, PLXNB1, PLXNB2, PLXNB3, PLXNC1, PLXND1, programmed cell death ligand 1, proprotein convertase PC9, P-selectin glycoprotein ligand-1, RAGE, reticulon 4, RF, RON-8, SEMA3A, SEMA3B, SEMA3C, SEMA3D, SEMA3E, SEMA3F, SEMA3G, SEMA4A, SEMA4B, SEMA4C, SEMA4D, SEMA4F, SEMA4G, SEMA5A, SEMA5B, SEMA6A, SEMA6B, SEMA6C, SEMA6D, SEMA7A, Shiga like toxin II, sphingosine-1-phosphate receptor-1, ST2, Staphylococcal lipoteichoic acid, tenascin, TG2, thymic stromal lymphopoietin receptor, TNF superfamily receptor 12A, transmembrane glycoprotein NMB, TREM-1, TREM-2, trophoblast glycoprotein, TSH receptor, TTR, tubulin, ULBP2, and receptors for hormones or growth factors.
The epitope, which means an antigenic determinant, contained in the antigen means a site on the antigen to which the antigen-binding domain in the antigen-binding molecule disclosed herein binds. Accordingly, for example, the epitope can be defined by its structure. Alternatively, the epitope may be defined by the antigen-binding activity of the antigen-binding molecule that recognizes the epitope. The epitope in an antigenic peptide or polypeptide may be determined by amino acid residues constituting the epitope. Alternatively, the epitope composed of a sugar chain may be determined by a particular sugar chain structure.
A linear epitope refers to an epitope comprising an epitope that is recognized via its primary sequence of amino acids. The linear epitope comprises typically at least 3 and most commonly at least 5, for example, approximately 8 to approximately 10 or 6 to 20 amino acids, in a unique sequence.
In contrast to the linear epitope, a conformational epitope refers to an epitope that is contained in a primary sequence of amino acids comprising a component other than the single defined component of the epitope to be recognized (e.g., an epitope whose primary sequence of amino acids may not be recognized by an antibody that determines the epitope). The conformational epitope may contain an increased number of amino acids, compared with the linear epitope. An antibody recognizes the conformational epitope by recognizing the three-dimensional structure of the antigenic peptide or protein. For example, the protein molecule may be folded to form a three-dimensional structure. In such a case, certain amino acids and/or polypeptide backbone constituting the conformational epitope are arranged in parallel to allow the antibody to recognize the epitope. The conformation of the epitope is determined by a method including, for example, but not limited to, X-ray crystallography, two-dimensional nuclear magnetic resonance spectroscopy, and site-specific spin labeling and electron paramagnetic resonance spectroscopy. See, for example, Epitope Mapping Protocols in Methods in Molecular Biology (1996), Vol. 66, Morris ed.
A method for confirming the binding of a test antigen-binding molecule containing an antigen-binding domain to IL-6R, to an epitope is mentioned below. A method for confirming the binding of a test antigen-binding molecule containing an antigen-binding molecule to an antigen other than IL-6R to an epitope can be appropriately performed in accordance with the following example.
For example, recognizing a linear epitope present in an IL-6R molecule by a test antigen-binding molecule containing an antigen-binding domain to IL-6R can be confirmed, for example, as follows. A linear peptide consisting of an amino acid sequence, which constitutes an extracellular domain of IL-6R, is synthesized for the above purpose. The peptide can be chemically synthesized or by genetic engineering method using a region encoding an amino acid sequence corresponding to the extracellular domain in cDNA of IL-6R. Then, the binding activity between the linear peptide (which consists of an amino acid sequence constituting the extracellular domain), and a test antigen-binding molecule, which contains an antigen-binding domain to IL-6R, is evaluated. For example, the binding activity of the antigen-binding molecule to the peptide can be evaluated by ELISA using the linear peptide immobilized as an antigen. Alternatively, the binding activity to the linear peptide is determined based on the level of inhibition by the linear peptide against the binding of the antigen-binding molecule to an IL-6R expression cell. By these tests, the binding activity of the antigen-binding molecule to the linear peptide can be determined.
Furthermore, recognizing a steric epitope by a test antigen-binding molecule containing an antigen-binding domain to IL-6R can be confirmed as follows. First, a cell expressing IL-6R is prepared for the above purpose. When the test antigen-binding molecule (containing an antigen-binding domain to IL-6R) is brought into contact with the IL-6R expression cell, if the test antigen-binding molecule strongly binds to the cell but the test antigen-binding molecule does not substantially bind to a linear peptide (which consists of an amino acid sequence constituting the extracellular domain of IL-6R and immobilized), recognition is made. Herein, the expression “does not substantially bind” means the case where the binding activity is 80% or less, usually 50% or less, preferably 30% or less, and particularly preferably 15% or less of the binding activity to a human IL-6R expression cell.
As a method for measuring the binding activity of a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) to the IL-6R expression cell, for example, the method described in the Antibodies A Laboratory Manual (Ed Harlow, David Lane, Cold Spring Harbor Laboratory (1988) 359-420) is mentioned. More specifically, the binding activity can be evaluated based on the principle of ELISA and FACS (fluorescence activated cell sorting) using an IL-6R expression cell as an antigen.
In the ELISA format, the binding activity of a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) to an IL-6R expression cell is quantitatively evaluated by comparing a signal level produced by an enzyme reaction. To explain more specifically, a test antigen-binding molecule is added to an ELISA plate, to which an IL-6R expression cell is immobilized. The test antigen-binding molecule bound to the cell is detected by an enzyme labeled antibody capable of recognizing the test antigen-binding molecule. In contrast, in FACS, a test antigen-binding molecule is serially diluted and the titer against the IL-6R expression cell is determined. In this manner, the binding activity of the test antigen-binding molecule to the IL-6R expression cell can be compared.
The binding of a test antigen-binding molecule to an antigen expressed on the surface of a cell suspended in a buffer, etc. can be detected by a flow cytometer. As the flow cytometer, for example, the following apparatuses are known.
FACSCalibur™ (all are trade names of products
manufactured by BD Biosciences)
Cell Lab Quanta/Cell Lab Quanta SC (all are trade names of products manufactured by Beckman Coulter)
As a preferable method for measuring the binding activity of a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) to an antigen, for example, the following method is mentioned. First, a test antigen-binding molecule is reacted with a cell expressing IL-6R and then stained by FITC-labeled secondary antibody recognizing the test antigen-binding molecule. If the test antigen-binding molecule is appropriately diluted with a preferable buffer, the antigen-binding molecule can be used in a desired concentration. For example, the antigen-binding molecule can be used in any concentration from 10 μg/ml to 10 ng/ml. Subsequently, fluorescent intensity and the number of cells are measured by FACSCalibur (manufactured by BD). The binding amount of antibody to the cells is analyzed by CELL QUEST Software (manufactured by BD). The binding amount is reflected in the fluorescent intensity obtained, in other words, a Geometric Mean value. To explain more specifically, the binding activity of a test antigen-binding molecule, which is represented by the binding amount of test antigen-binding molecule, can be measured by obtaining the Geometric Mean value.
Whether a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) shares an epitope with another antigen-binding molecule, can be confirmed by a competition test between both antigen-binding molecules to the same epitope. The competition between the antigen-binding molecules is detected by a crossover blocking assay, etc. For example, a competitive ELISA assay is a preferable crossover blocking assay.
The crossover blocking assay is specifically performed as follows. IL-6R protein is applied onto the wells of a microtiter plate and pre-incubated in the presence or absence of a competitive antigen-binding molecule serving as a candidate. Thereafter, a test antigen-binding molecule is added. The amount of test antigen-binding molecule bound to IL-6R protein in a well indirectly correlates with the binding ability of the candidate-competitive antigen-binding molecule, which competitively binds to the same epitope. In other words, the larger the affinity of a competitive antigen-binding molecule to the same epitope, the lower the binding activity of the test antigen-binding molecule to IL-6R protein applied to a well.
The amount of test antigen-binding molecule bound to a well via an IL-6R protein can be easily measured by labelling the test antigen-binding molecule in advance. For example, an antigen-binding molecule labeled with biotin is measured by using an avidin-peroxidase conjugate and an appropriate substrate. A crossover blocking assay using an enzyme label such as peroxidase is particularly called as a competitive ELISA assay. The test antigen-binding molecule may be labeled with another detectable or measurable labeling substance. For example, a radio label or a fluorescent label is known in the art.
Relative to the binding activity obtained in a control test, which is performed in the absence of a candidate competitive antigen-binding molecule, if the binding of a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) can be blocked by the competitive antigen-binding molecule in a percentage of at least 20%, preferably at least 20-50%, and further preferably at least 50%, it is determined that the test antigen-binding molecule binds to substantially the same epitope or is a competitive antigen-binding molecule binding to the same epitope.
When the structure of the epitope, to which a test antigen-binding molecule (containing an antigen-binding domain to IL-6R) is bound, is identified, sharing the same epitope by a test antigen-binding molecule and a control antigen-binding molecule can be evaluated by comparing the binding activities of both antigen-binding molecules to a peptide, which is prepared by introducing an amino acid mutation to the peptide constituting the epitope.
Such a binding activity can be measured, for example, if an ELISA format is used, by a method of comparing binding activities of the test antigen-binding molecule and the control antigen-binding molecule to a linear peptide having a mutation introduced therein. Other than ELISA, the binding activity can be measured by a method of determining the binding activities of a test antigen-binding molecule and a control antigen-binding molecule to the mutant peptide by passing these antigen biding molecules through a column, to which a mutant peptide as mentioned above is bound, and quantifying each of the antigen-binding molecules released in an eluant. The mutant peptide is fused with e.g., GST and adsorbed to a column as a fusion peptide is known in the art.
Furthermore, when the epitope identified is a steric epitope, sharing the epitope by a test antigen-binding molecule as well as a control antigen-binding molecule can be evaluated by the following method. First, a cell expressing IL-6R and a cell expressing IL-6R having an epitope to which a mutation is introduced are prepared. These cells are suspended in an appropriate buffer such as PBS. To the cell suspension solution, the test antigen-binding molecule and the control antigen-binding molecule are added. Then, the cell suspension solution is appropriately washed with a buffer. To the cell suspension solution, an FITC-labeled antibody capable of recognizing the test antigen-binding molecule and the control antigen-binding molecule, is added. The fluorescent intensity and the number of cells stained with the labeled antibody are measured by FACSCalibur (manufactured by BD). The test antigen-binding molecule and the control antigen-binding molecule are appropriately diluted with a preferable buffer to prepare solutions having a desired concentration and then put in use. The concentration to be used falls within the range, for example, from 10 μg/ml to 10 ng/ml. The binding amount of labelled antibody to the cells is reflected in the fluorescent intensity, more specifically, the Geometric Mean value, which is obtained by analyzing by CELLQUEST Software (manufactured by BD). In other words, the binding activities of the test antigen-binding molecule and the control antigen-binding molecule (which are expressed by the binding amounts of labelled antibody) can be measured by obtaining the Geometric Mean value.
In this method, for example “substantially not binding to a mutant IL-6R expression cell” can be determined by the following method. First, a test antigen-binding molecule and a control antigen-binding molecule bound to a cell expressing mutant IL-6R are stained with a labelled antibody. Then, the fluorescent intensity of the cell is detected. When fluorescence is detected by use of FACSCalibur for flow cytometry, the obtained fluorescent intensity can be analyzed by CELL QUEST Software. Based on the Geometric Mean values obtained in the presence and absence of the antigen-binding molecule, the comparison value (ΔGeo-Mean) is calculated based on the following computation expression. In this way, the ratio of fluorescent intensity increased by binding of the antigen-binding molecule can be obtained.
ΔGeo-Mean=Geo-Mean (in the presence of antigen-binding molecule)/Geo-Mean (in the absence of antigen-binding molecule)
The Geometric Mean comparison value (mutant IL-6R Molecule ΔGeo-Mean value), in which the binding amount of the test antigen-binding molecule to the mutant IL-6R expression cell (obtained by analysis) is reflected, is compared with the ΔGeo-Mean comparison value, in which the binding amount of test antigen-binding molecule to the IL-6R expression cell is reflected. In this case, it is particularly preferable that the concentrations of the test antigen-binding molecules to be used for obtaining ΔGeo-Mean comparison value with respect to the mutant IL-6R expression cell and the IL-6R expression cell are controlled to be the same or substantially the same with each other. The antigen-binding molecule, which is previously confirmed to recognize the epitope of IL-6R, is used as a control antigen-binding molecule.
If the ΔGeo-Mean comparison value of a test antigen-binding molecule to a mutant IL-6R expression cell relative to the ΔGeo-Mean comparison value of the test antigen-binding molecule to an IL-6R expression cell is at least 80%, preferably 50%, further preferably 30%, particularly preferably smaller than 15%, the antigen-binding molecule is determined as “substantially not binding to a mutant IL-6R expression cell”. The computation expression for obtaining a Geo-Mean value (Geometric Mean) is described in the CELL QUEST Software User's Guide (BD biosciences). If the binding amounts are substantially equivalent by comparing the ΔGeo-Mean comparison values, it can be evaluated that the test antigen-binding molecule and the control antigen-binding molecule bind to the same epitope.
In the specification, as the “antigen-binding domain”, a domain of any structure can be used as long as it binds to a desired antigen. Preferable examples of such a domain include a variable region of a heavy chain or light chain of an antibody; a module (WO2004/044011, WO2005/040229) of approximately 35 amino acids called A domain and contained in Avimer (a cell membrane protein present in vivo); Adnectin (WO2002/032925) containing a 10Fn3 domain, which is a domain binding to a protein in fibronectin (a glycoprotein expressed in cell membrane); Affibody (WO1995/001937), composed of a three-helix bundle consisting of 58 amino acids of Protein A and based on the scaffold of an IgG binding domain; DARPins (Designed Ankyrin Repeat proteins) (WO2002/020565), which is a region exposed in the molecular surface of ankyrin repeat (AR) containing 33 amino acid residues and having a structure formed by repeatedly laminating a subunit consisting of a turn, two antiparallel helixes and a loop; Anticalin, etc. (WO2003/029462), which is a four-loop regions supporting one side of a barrel structure in which 8 highly-conserved antiparallel strands are twisted toward the center axis, in a lipocalin molecule such as neutrophil gelatinase-associated lipocalin (NGAL); and a depressed region (WO2008/016854) of a parallel sheet structure within a horseshoe-shaped structure, which is formed by repeatedly laminating a leucine-rich-repeat (LRR) module of a variable lymphocyte receptor (VLR) having no immunoglobulin structure, as the acquired immune system of a jawless vertebrate such as lamprey and hagfish. As a preferable example of the antigen-binding domain used in the present invention, an antigen-binding domain containing a variable region of a heavy chain and a light chain of an antibody is mentioned. As an example of such an antigen-binding domain, e.g., “scFv (single chain Fv)”, “single chain antibody”, “Fv”, “scFv2 (single chain Fv 2)”, “diabody”, “Fab”, “F(ab′)2”, domain antibody (dAb) (WO2004/058821, WO2003/002609), scFv-sc (WO2005/037989) or Fc fusion protein is preferably mentioned. In the molecule containing an Fc region, the Fc region can be used as a binding domain for FcRn (particularly human FcRn). Also, a molecule prepared by fusing such a molecule with a human FcRn binding domain can be used.
Antigen-binding domains in the antigen-binding molecules of the present invention can be bound to the same epitope. The same epitope used herein can be present in the protein consisting of an amino acid sequence represented by, for example, SEQ ID NO: 1 (IL-6R_PP; NP—000556.1); more specifically, can be present in the protein consisting of 20th to 365th amino acids of the amino acid sequence represented by SEQ ID NO: 1. Alternatively, an antigen-binding domain in the antigen-binding molecule of the present invention can bind to mutually different epitopes. The different epitopes herein can be present in the protein consisting of, for example, the amino acid sequence represented by SEQ ID NO: 1; more specifically, can be present in the protein consisting of 20th to 365th amino acid of the amino acid sequence represented by SEQ ID NO: 1. For this purpose, an antigen-binding domain contained in a bispecific antibody can be appropriately used. The bispecific antibody refers to an antibody having variable regions recognizing different epitopes in the same antibody molecule. The bispecific antibody may be an antibody recognizing two or more different antigens and may be an antibody recognizing two or more different epitopes present on the same antigen.
As the antigen-binding domain of the present invention, a domain of a receptor protein binding to a target (antigen) and involved in binding to the target (antigen) can be preferably used. More specifically, the antigen-binding molecule may be a protein prepared by fusing a binding domain to FcRn (in particular, FcRn) and a sugar chain receptor-binding domain with a receptor protein binding to a target (antigen). Examples of such an antigen-binding molecule include TNFR-Fc fusion protein, IL1R-Fc fusion protein, VEGFR-Fc fusion protein and CTLA4-Fc fusion protein (Nat Med. (2003) 9 (1), 47-52, BioDrugs. (2006) 20 (3), 151-160). Even if the antigen-binding molecule of the present invention is a fusion protein formed of such a receptor protein, a binding domain to FcRn (particularly human FcRn), as long as the antigen-binding molecule changes the binding activity to a target molecule depending upon the ion-concentration condition and as long as the antigen-binding molecule has the binding activity to a sugar chain receptor and to FcRn (particularly human FcRn), the antigen-binding molecule can promote uptake of an antigen into a cell. Furthermore, the antigen-binding molecule, if it is administered, can promote a decrease of the antigen concentration in plasma. Moreover, the pharmacokinetics of such an antigen-binding molecule is improved and the number of antigens, to which a single antigen-binding molecule can bind, can be increased.
Furthermore, as the antigen-binding domain of the present invention, a domain of a natural or artificial ligand binding to a target and involved in binding to the target can be preferably used. More specifically, the antigen-binding molecule may also be a molecule prepared by fusing an FcRn binding domain (particularly, FcRn) and a sugar chain receptor-binding domain with a natural or artificial protein ligand, which binds to a target and has an antagonist activity and a neutralization effect. Of these antigen-binding domains, as an artificial ligand, for example, an artificial ligand such as mutant IL-6 (EMBO J. (1994) 13 (24), 5863-70) is mentioned. Even if the antigen-binding molecule of the present invention is a fusion molecule with such an artificial ligand, as long as the antigen-binding molecule changes the binding activity to a target molecule depending upon the ion-concentration condition and as long as the antigen-binding molecule has the binding activity to a sugar chain receptor and to FcRn (particularly human FcRn), the antigen-binding molecule can promote uptake of an antigen into a cell. Furthermore, the antigen-binding molecule, if it is administered, can promote a decrease of the antigen concentration in plasma. Moreover, the pharmacokinetics of such an antigen-binding molecule is improved and the number of antigens to which a single antigen-binding molecule can bind can be increased.
Specificity refers to the state where one of the molecules specifically bind to each other does not show a significant binding to any other molecule except the other bonding partner(s). Alternatively, in the case where an antigen-binding domain is specific to a certain epitope among a plurality of epitopes contained in a certain antigen, the term “specificity” is used. In the case where an epitope (to which an antigen-binding domain binds) is contained in a plurality of different antigens, an antigen-binding molecule having the antigen-binding domain can bind to various antigens containing the epitope.
In the specification, the antibody refers to a natural or partial or completely synthesized immunoglobulin. The antibody can be isolated from a natural source in which a natural antibody is present, such as plasma and serum, from the supernatant of a culture of a hybridoma cell producing an antibody, or can be partially or completely synthesized by a genetic recombination technique, etc. As examples of the antibody, immunoglobulin isotypes and subclasses of these isotypes are preferably mentioned. As the human immunoglobulins, 9 classes (isotypes) are known, which include IgG1, IgG2, IgG3, IgG4, IgA1, IgA2, IgD, IgE and IgM, Of these isotypes, IgG1, IgG2, IgG3 and IgG4 can be included in the antibodies of the present invention.
A method for preparing an antibody having a desired binding activity is known to those skilled in the art. A method for preparing an antibody (anti-IL-6R antibody) binding to IL-6R will be illustrated. An antibody binding to an antigen except IL-6R can be appropriately prepared in accordance with the method illustrated below.
An anti-IL-6R antibody can be obtained as a polyclonal or a monoclonal antibody by use of a known means. As the anti-IL-6R antibody, a monoclonal antibody derived from a mammalian animal is preferably prepared. The monoclonal antibody derived from a mammalian animal includes a monoclonal antibody produced from a hybridoma and a monoclonal antibody produced from a host cell transformed by an expression vector containing an antibody gene in accordance with a genetic engineering method. Note that a “humanized antibody” and a “chimeric antibody” are included in the monoclonal antibody of the present invention.
A hybridoma producing a monoclonal antibody can be prepared by use of a technique known in the art, for example, as follows. First, a mammalian animal is immunized with an IL-6R protein used as a sensitizing antigen in accordance with a conventional immunization method. The obtained immunocyte is fused with a parent cell known in the art in accordance with a conventional cell fusion method. Then, a monoclonal antibody-producing cell is screened by a conventional screening method. In this manner, a hybridoma producing an anti-IL-6R antibody can be selected.
Specifically, a monoclonal antibody is prepared, for example, as follows. First, an IL-6R gene, whose nucleotide sequence is disclosed in SEQ ID NO: 2 (IL-6R_PN; NM—000565.3), is allowed to be expressed to obtain IL-6R protein (represented by SEQ ID NO: 1) to be used as a sensitizing antigen for obtaining an antibody. To describe more specifically, an appropriate host cell is transformed by inserting an IL-6R encoding gene sequence into a known expression vector. A desired human IL-6R protein is purified by a known method from the host cell or the culture supernatant. To obtain soluble IL-6R from the culture supernatant, for example, soluble IL-6R as described in Mullberg et al. (J. Immunol. (1994) 152 (10), 4958-4968), i.e., a protein consisting of 1st to 357th amino acids of the IL-6R polypeptide sequence represented by SEQ ID NO: 1, is expressed in place of the IL-6R protein represented by SEQ ID NO: 1. Also, a purified natural IL-6R protein can be used as a sensitizing antigen.
As a sensitizing antigen for use in immunization of a mammalian animal, the purified IL-6R protein can be used. Also, a partial IL-6R peptide can be used as a sensitizing antigen. At this time, the partial peptide can be also obtained by chemical synthesis based on the amino acid sequence of human IL-6R or obtained by inserting a part of an IL-6R gene into an expression vector and expressing the vector. The region and size of the IL-6R peptide used as a partial peptide are not particularly limited. As a preferable region, an arbitrary sequence that can be selected from the amino acid sequence corresponding to 20-357th amino acids of the amino acid sequence (represented by SEQ ID NO: 1) can be used. The number of amino acids constituting a peptide serving as a sensitizing antigen is preferably at least 5 or more, for example, 6 or more, or 7 or more; more specifically, a peptide having 8 to 50 residues and preferably 10 to 30 residues can be used as a sensitizing antigen.
A fusion protein prepared by fusing a desired partial polypeptide or peptide of an IL-6R protein with a different polypeptide can be used as a sensitizing antigen. To produce the fusion protein to be used as a sensitizing antigen, for example, an Fc fragment of an antibody and a peptide tag can be preferably used. The vector for expressing the fusion protein can be prepared by fusing genes encoding desired two types or more polypeptide fragments in frame and inserting the fusion gene in an expression vector as described above. A method for preparing a fusion protein is described in Molecular Cloning 2nd ed. (Sambrook, J et al., Molecular Cloning 2nd ed., 9.47-9.58 (1989) Cold Spring Harbor Lab. press). A method for obtaining IL-6R used as a sensitizing antigen and an immunization method using IL-6R are specifically described in WO2003/000883, WO2004/022754 and WO2006/006693, etc.
The mammalian animal to be immunized with the sensitizing antigen is not limited to a specific animal and is preferably selected in view of compatibility to the parent cell to be used in cell fusion. Generally, an animal belonging to the rodent family such as a mouse, a rat and a hamster or an animal such as a rabbit or a monkey is preferably used.
An animal as mentioned above is immunized by a sensitizing antigen in accordance with a known method. A mammalian animal is immunized by a general method such as intraperitoneally or subcutaneously injection of a sensitizing antigen. To describe more specifically, a sensitizing antigen is diluted with e.g., PBS (Phosphate-Buffered Saline) or physiological saline at an appropriate dilution rate, if desired, a conventional adjuvant, for example, Freund complete adjuvant, is added thereto, and emulsified, and thereafter, administered to a mammalian animal several times every 4 to 21 days. In immunization with a sensitizing antigen, an appropriate carrier can be used. Particularly when a small molecular-weight partial peptide is used as a sensitizing antigen, the sensitizing antigen is joined to a carrier protein, such as albumin and keyhole limpet hemocyanin, to prepare a sensitizing antigen peptide, which is desirably used for immunization.
Furthermore, a hybridoma producing a desired antibody can be also prepared by use of DNA immunization in accordance with the following manner. DNA immunization is an immunization method of giving immunostimulation by administering vector DNA (which is constructed such that an antigen protein-encoding gene is expressed in an immunized animal) to the animal to be immunized and allowing a sensitizing antigen to express in the immunized animal, in-vivo. Compared to a general immunization method of administering a protein antigen to an animal to be immunized, the DNA immunization has the following advantages:
To obtain the monoclonal antibody of the present invention by DNA immunization, first, DNA expressing an IL-6R protein is administered to the animal to be immunized. IL-6R-encoding DNA can be synthesized by a known method such as PCR. The obtained DNA is inserted to an appropriate expression vector and then administered to the animal to be immunized. As the expression vector, for example, a commercially available expression vector such as pcDNA3.1 can be preferably used. As a method for administering a vector to a living body, a method commonly used can be employed. For example, gold particles on which an expression vector is adsorbed are introduced by a gene gun into animal cells to be immunized. In this manner, DNA immunization is performed. An antibody recognizing IL-6R can be also prepared by use of a method described in International Publication WO2003/104453.
As described above, a mammalian animal is immunized. After an increase of titer of an antibody binding to IL-6R in the serum is confirmed, immunocytes are taken from the mammalian animal and subjected to cell fusion. As preferable immunocytes, particularly, spleen cells can be used.
As the cells to be fused with the immunocytes, mammalian myeloma cells are used. It is preferable that the myeloma cells have an appropriate selection marker for screening. The selection marker refers to a trait that can be maintained (or cannot be maintained) in specific culture conditions. As a selection marker, e.g., hypoxanthine-guanine-phosphoribosyltransferase defective (hereinafter abbreviated as HGPRT defective) marker or a thymidine kinase defective (hereinafter abbreviated as TK defective) marker is known. A HGPRT or TK defective cell has hypoxanthine-aminopterin-thymidine sensitivity (hereinafter abbreviated as HAT sensitivity). A HAT sensitive cell cannot synthesize DNA in a HAT selection medium and die; however, if the HAT sensitive cell is fused with a normal cell, DNA synthesis can be continued by use of salvage pathway of the normal cell. With this mechanism, the HAT sensitive cell comes to grow even in a HAT selection medium.
HGPRT defective and TK defective cells can be selected in mediums containing 6 thioguanine and 8 azaguanine (hereinafter abbreviated as 8AG), respectively or in a medium containing 5′ bromodeoxyuridine. Normal cells, which can take these pyrimidine analogues into DNA, die, whereas cells, which lack enzymes and thus cannot take these pyrimidine analogues, can survive in a selection medium. Other than these, a selection marker called a G418 resistant is resistant against 2-deoxystreptamine antibiotic substance (gentamicin analogue) due to the presence of a neomycin resistant gene. Various myeloma cells suitably used for cell fusion are known in the art.
Examples of such myeloma cells that can be preferably used include P3 (P3x63Ag8.653) (J. Immunol. (1979) 123 (4), 1548-1550), P3x63Ag8U.1 (Current Topics in Microbiology and Immunology (1978) 81, 1-7), NS-1 (C. Eur. J. Immunol. (1976) 6 (7), 511-519), MPC-11 (Cell (1976) 8 (3), 405-415), SP2/0 (Nature (1978) 276 (5685), 269-270), FO (J. Immunol. Methods (1980) 35 (1-2), 1-21), S194/5.XXO.BU.1 (J. Exp. Med. (1978) 148 (1), 313-323) and R210 (Nature (1979) 277 (5692), 131-133).
An immunocyte as mentioned above and a myeloma cell are fused basically in accordance with a known method, for example, a method of Kohler and Milstein, et al. (Methods Enzymol. (1981)73, 3-46). More specifically, the cell fusion can be performed in a general nutrition culture solution in the presence of, e.g., a cell fusion accelerator. Examples of the fusion accelerator that can be used include polyethylene glycol (PEG) and Sendai virus (HVJ). To further increase a fusion efficiency, if desired, an adjuvant such as dimethylsulfoxide is added.
The ratio of the immunocytes and myeloma cells to be used can be set arbitrarily. For example, the ratio of immunocytes relative to the myeloma cells is preferably 1 to 10. As the culture solution to be used for the cell fusion, for example, RPMI1640 culture solution and MEM culture solution suitable for proliferation of the myeloma cell strain and other conventional culture solutions for use in culturing such fusion cells, are used. Furthermore, a serum complemental liquid such as fetal bovine serum (FCS), can be preferably added.
Cell fusion is performed as follows. First, predetermined amounts of immunocytes and myeloma cells are mixed well in the culture solution. To the mixture, a PEG solution (for example, average molecular weight of approximately 1000 to 6000) previously heated to approximately 37° C. and usually having a concentration of 30 to 60% (w/v), is added. The solution mixture is gently mixed to form a desired fusion cell (hybridoma). Then, an appropriate culture solution as mentioned above is sequentially added. The mixture is centrifuged and the supernatant is removed. This operation is repeated to remove a cell fusion agent, etc., which are unfavorable for hybridoma growth.
The hybridoma thus obtained can be selected by culturing it in a conventional selective culture solution such as a HAT culture solution (culture solution containing hypoxanthine, aminopterin and thymidine). The culture can be continued in the HAT culture solution for a sufficient time (usually, several day to several weeks) until cells (nonfusion cells) except a desired hybridoma die. Subsequently, screening and monocloning of a hybridoma producing a desired antibody are performed by conventional limiting dilution method.
The hybridoma thus obtained can be selected by use of a selective culture solution in accordance with the selection marker that the myeloma used in cell fusion has. For example, cells defective in e.g., HGPRT and TK can be screened by culturing them in a HAT culture solution (culture solution containing hypoxanthine, aminopterin and thymidine). In other words, when a HAT sensitive myeloma cell is used in cell fusion, the cell successively fused with a normal cell can selectively grow in the HAT culture solution. The culture is continued for a sufficient time until cells (nonfusion cells) except a desired hybridoma die in the HAT culture solution. More specifically, a desired hybridoma can be generally selected by culturing for several days to several weeks. Subsequently, screening and monocloning of a hybridoma producing a desired antibody are carried out by a conventional limiting dilution method.
Screening and monocloning of a desired antibody can be preferably performed by a screening method based on an antigen antibody reaction known in the art. For example, a monoclonal antibody binding to IL-6R can be bound to IL-6R expressed on a cell surface. Such a monoclonal antibody can be screened, for example, by FACS (fluorescence activated cell sorting). FACS is a system, which can analyze binding of an antibody to a cell surface, by bringing cells into contact with a fluorescent antibody, applying laser light to the cells, and measuring fluorescence emitted from individual cells.
To screen a hybridoma producing the monoclonal antibody of the present invention by FACS, first, a cell expressing IL-6R is prepared. A preferable cell for screening is a mammalian animal cell in which IL-6R is forcibly expressed. By using a mammalian animal cell (serving as a host cell) not transformed as a control, the binding activity of an antibody against IL-6R on a cell surface can be selectively detected. More specifically, a hybridoma producing an antibody, which does not bind to a host cell but binds to the cell forcibly expressing IL-6R, is selected to obtain a hybridoma producing an IL-6R monoclonal antibody.
The binding activity of an antibody against IL-6R expression cell (immobilized) can be evaluated based on the principle of ELISA. For example, an IL-6R expression cell is immobilized to wells of an ELISA plate. The supernatant of a hybridoma culture is brought into contact with the immobilized cell in the wells. In this manner, an antibody bound to the immobilized cell is detected. When the monoclonal antibody is derived from a mouse, the antibody bound to the cell can be detected by an anti-mouse immunoglobulin antibody. The hybridoma producing a desired antibody having a binding ability to an antigen and selected by the screening can be cloned by a limiting dilution method, etc.
The hybridoma producing a monoclonal antibody and prepared as mentioned above can be subcultured in a conventional culture solution. Furthermore, the hybridoma can be stored in liquid nitrogen for a long time.
The hybridoma is cultured in accordance with a conventional method. From the culture supernatant, a desired monoclonal antibody can be obtained. Alternatively, the hybridoma is administered to a mammalian animal having a compatibility with it and grown therein. From the ascitic fluid, a monoclonal antibody can be obtained. The former method is preferable to obtain a high-purity antibody.
An antibody encoded by an antibody gene, which is cloned from an antibody-producing cell such as the hybridoma, can be preferably used. The antibody gene cloned is incorporated into an appropriate vector and then introduced into a host. In this manner, the antibody encoded by the gene is expressed. The methods for isolating an antibody gene, for introducing the antibody gene into a vector, and for transforming a host cell have been already established, for example, by Vandamme et al. (Eur. J. Biochem. (1990)192 (3), 767-775). Also, a method for producing a recombinant antibody is known in the art, as described below.
To describe more specifically, cDNA encoding a variable region (V region) of the anti-IL-6R antibody is obtained from a hybridoma cell producing an anti-IL-6R antibody. For this purpose, usually, total RNA is first extracted from the hybridoma. As a method for extracting mRNA from a cell, for example, the following methods can be used.
The mRNA extracted can be purified by an mRNA Purification Kit (manufactured by GE Healthcare), etc. Alternatively, mRNA can be obtained from a hybridoma by use of a commercially available kit (for directly extracting total mRNA from a cell) such as QuickPrep mRNA Purification Kit (manufactured by GE Healthcare). From the obtained mRNA, cDNA encoding an antibody V region can be synthesized by using a reverse transcriptase. Such cDNA can be synthesized by use of an AMV Reverse Transcriptase First-strand cDNA Synthesis kit (manufactured by SEIKAGAKU CORPORATION). For synthesis and amplification of cDNA, a SMART RACE cDNA amplification kit (manufactured by Clontech) and 5′-RACE method using a PCR (Proc. Natl. Acad. Sci. USA (1988) 85 (23), 8998-9002, Nucleic Acids Res. (1989) 17 (8), 2919-2932) can be appropriately used. Furthermore, in the process for synthesizing cDNA, appropriate restriction enzyme sites (described later) can be introduced into both terminals of the cDNA.
From the obtained PCR product, a desired cDNA fragment is purified and then ligated to vector DNA. A recombinant vector is prepared in this manner and introduced in Escherichia coli, etc. After a colony is selected, a desired recombinant vector can be prepared from Escherichia coli forming the colony. Subsequently, whether the recombinant vector has the nucleotide sequence of a desired cDNA or not is determined by a known method, for example, a dideoxynucleotide chain termination method, etc.
To obtain a variable region-encoding gene, it is convenient to use 5′-RACE method using a variable region gene amplification primer. First, cDNA is synthesized by using RNA extracted from a hybridoma cell as a template, and then, 5′-RACE cDNA library is obtained. For constructing the 5′-RACE cDNA library, a commercially available kit such as a SMART RACE cDNA amplification kit, is appropriately used.
Using the obtained 5′-RACE cDNA library as a template, an antibody gene is amplified by a PCR method. Based on a known antibody gene sequence, primers for amplifying a mouse antibody gene can be designed. The nucleotide sequences of the primers vary depending upon the subclass of immunoglobulin. Therefore, it is desirable to previously determine the subclass by use of a commercially available kit such as Iso Strip mouse monoclonal antibody isotyping kit (Roche Diagnostics).
To describe it more specifically, in order to obtain, for example, a mouse IgG-encoding gene, the primer capable of amplifying genes encoding γ1, γ2 a, γ2b and γ3 as heavy chains, and K chain and 2 chain as light chains can be used. In order to amplify an IgG variable-region gene, a primer annealing to a portion corresponding to a constant region near a variable region is generally used as a 3′-side primer. In contrast, as a 5′-side primer, a primer attached to a 5′ RACE cDNA library preparation kit is used.
Using the PCR product thus amplified, an immunoglobulin formed of a combination of heavy chains and light chains can be reconstituted. A desired antibody can be screened based on the binding activity of the reconstituted immunoglobulin to IL-6R. For example, when an antibody against IL-6R is desired, it is further preferable that the binding of the antibody to IL-6R is specific. The antibody binding to IL-6R can be screened, for example, as follows:
(1) a step of bringing an antibody, which contains a V region encoded by the cDNA obtained from a hybridoma, into contact with an IL-6R expression cell,
(2) a step of detecting binding between the IL-6R expression cell and the antibody, and
(3) a step of selecting the antibody binding to the IL-6R expression cell.
A method for detecting the binding between the antibody and the IL-6R expression cell is known in the art. More Specifically, the binding between the antibody and the IL-6R expression cell can be detected by a method such as FACS as mentioned above. To evaluate the binding activity of the antibody, a preparation on which IL-6R expression cells are fixed can be appropriately used.
As a method for screening an antibody based on the binding activity, a panning method using a phage vector is preferably used. When an antibody gene is obtained as a library of a subclass such as a heavy chain and a light chain from a polyclonal antibody expression cells, a screening method using a phage vector is advantageously used.
If genes encoding variable regions of a heavy chain and a light chain are ligated via an appropriate linker sequence, a single chain Fv (scFv) (Nat. Biotechnol. (2005) 23 (9), 1126-1136) can be formed. If the scFv-encoding gene is inserted to a phage vector, a phage expressing a scFv on the surface can be obtained. After the phage is brought into contact with a desired antigen, the phage bound to the antigen is recovered to obtain scFv-encoding DNA having a desired binding activity. This operation is repeated, if necessary, to concentrate scFv having a desired binding activity.
After cDNA encoding a V region of a desired anti-IL-6R antibody is obtained, the cDNA is digested with a restriction enzyme(s), which recognize the restriction enzyme sites inserted to both terminals of the cDNA. A restriction enzyme preferably recognizes and digests a nucleotide sequence that less frequently emerges in the nucleotide sequence constituting an antibody gene. In order to insert a single copy digestion fragment into a vector in a right direction, use of a restriction enzyme providing sticky ends is preferable. An antibody expression vector can be obtained by inserting cDNA encoding a V region of the anti-IL-6R antibody digested as mentioned above into an appropriate expression vector. At this time, if an antibody constant region (C region)-encoding gene and a gene encoding the V region are fused in frame, a chimeric antibody is obtained. The chimeric antibody herein refers to an antibody having a constant region and a variable region derived from different origins. Accordingly, in addition to a xenogeneic chimeric antibody such as a mouse-human chimeric antibody, a human-human homogeneous chimeric antibody is included in the chimeric antibody defined in the present invention. By inserting the V region gene into an expression vector already having a constant region, a chimeric antibody expression vector can be constructed. To explain it more specifically, for example, on the 5′ side of the expression vector having DNA encoding a desired antibody constant region (C region), the sequence recognized by a restriction enzyme digesting the V region gene can be appropriately arranged. Both fragments digested by the same combination of restriction enzymes are fused in frame to construct a chimeric antibody expression vector.
To produce an anti-IL-6R monoclonal antibody, the antibody gene is inserted into an expression vector such that the antibody gene can be expressed under the control of an expression control region. The expression control region for expressing the antibody contains, for example, an enhancer and a promoter. In addition, an appropriate signal sequence can be added to the amino terminal so as to secrete an expressed antibody out of the cell. In Examples (described later), a peptide having an amino acid sequence MGWSCIILFLVATATGVHS (SEQ ID NO: 3) is used as a signal sequence. Other than this, an appropriate signal sequence is added. The polypeptide expressed is cleaved at the carboxyl terminal of the above sequence and the cleaved polypeptide can be secreted as a mature polypeptide out of the cell. Subsequently, an appropriate host cell is transformed by the expression vector to obtain a recombinant cell expressing an anti-IL-6R antibody-encoding DNA.
To express an antibody gene, DNAs encoding an antibody heavy chain (H-chain) and an antibody light chain (L-chain), respectively, are integrated into different expression vectors. A host cell is simultaneously transformed (co-transfected) with the vectors having the H-chain and the L-chain, respectively integrated therein to express an antibody molecule having the H-chain and L-chain. Alternatively, DNAs respectively encoding a H-chain and a L-chain are integrated into a single expression vector and then introduced to a host cell. In this manner, the host cell can be transformed (see, International Publication WO 1994/011523).
For preparing antibodies by introducing an isolated antibody gene into an appropriate host, various combinations of host cells and expression vectors are known in the art. These expression systems all can be applied to isolating the antigen-binding domain of the present invention. When an eukaryotic cell is used as a host cell, an animal cell, a plant cell or a fungus cell can be appropriately used. As the animal cell, for example, the following cells can be illustrated
(1) Mammalian cells: CHO, COS, myeloma, BHK (baby hamster kidney), Hela, Vero, HEK (human embryonic kidney) 293, etc.
(2) Amphibian cells: Xenopus oocyte, etc.
(3) Insect cells: sf9, sf21, Tn5, etc.
Alternatively, antibody gene expression systems using cells derived from the genus Nicotiana (e.g., Nicotiana tabacum) as the plant cells are known in the art. Cultured callus cells can be appropriately used for the plant cell transformation.
The following cells can be used as the fungus cells:
Also, antibody gene expression systems using prokaryotic cells are known in the art. In the case of using, for example, bacterial cells, cells of bacteria such as E. coli and Bacillus subtilis can be appropriately used. The expression vectors comprising the antibody gene of interest are transferred into these cells by transformation. The transformed cells are cultured in vitro, and the desired antibody can be obtained from the resulting cultures of the transformed cells.
In addition to the host cells, transgenic animals may be used for the recombinant antibody production. Specifically, the desired antibody can be obtained from animals transfected with the gene encoding this antibody. For example, the antibody gene can be inserted in frame into genes encoding proteins specifically produced in milk to construct fusion genes. For example, goat β casein can be used as the proteins secreted into milk. DNA fragments comprising the fusion genes having the antibody gene inserted are injected into goat embryos, which are in turn introduced into female goats. From milk produced by transgenic goats (or progeny thereof) brought forth by the goats that have received the embryos, the desired antibody can be obtained as a fusion protein with the milk protein. In addition, hormone can be administered to the transgenic goats in order to increase the amount of milk containing the desired antibody produced from the transgenic goats (Bio/Technology (1994), 12 (7), 699-702).
In the case of administering the antigen-binding molecule described herein to humans, an antigen-binding domain derived from a genetically recombinant antibody that has been engineered artificially can be appropriately adopted as an antigen-binding domain for the antigen-binding molecule, for example, for the purpose of reducing heteroantigenicity in humans. The genetically recombinant antibody encompasses, for example, humanized antibodies in addition to the chimera antibodies described above. These engineered antibodies are appropriately produced using a method known in the art.
Each antibody variable region used for preparing the antigen-binding domain in the antigen-binding molecule described herein is typically composed of three complementarity-determining regions (CDRs) flanked by four framework regions (FRs). The CDRs are regions that substantially determine the binding specificity of the antibody. The CDRs have diverse amino acid sequences. On the other hand, the FRs are mostly constituted by amino acid sequences that are highly identical even among antibodies differing in binding specificity. Therefore, it is considered that in general, the binding specificity of a certain antibody can be transplanted to other antibodies through CDR grafting.
The humanized antibodies are also called reshaped human antibodies. Specifically, for example, a humanized antibody consisting of a non-human animal (e.g., mouse) antibody CDR-grafted human antibody is known in the art. General gene recombination approaches are also known for obtaining the humanized antibodies. Specifically, for example, overlap extension PCR is known in the art as a method for grafting mouse antibody CDRs to human FRs. In the overlap extension PCR, a nucleotide sequence encoding each mouse antibody CDR to be grafted is added to primers for human antibody FR synthesis. The primers are prepared with respect to each of the four FRs. For grafting the mouse CDRs to the human FRs, it is generally regarded as advantageous to select human FRs highly identical to mouse FRs, in order to maintain the CDR functions. Specifically, in general, human FRs comprising amino acid sequences highly identical to those of FRs adjacent to the mouse CDRs to be grafted are preferably used.
The nucleotide sequences to be linked are designed so that the sequences are connected in frame with each other. The human FR-encoding nucleotide sequences are individually synthesized using their respective primers. The resulting products contain the mouse CDR-encoding DNA added to each human FR-encoding sequence. The mouse CDR-encoding nucleotide sequences are designed so that the nucleotide sequence in each product overlaps with another. Subsequently, the overlapping CDR portions in the products synthesized with human antibody genes as templates are annealed to each other for complementary strand synthesis reaction. Through this reaction, the human FR sequences are linked via the mouse CDR sequences.
Finally, the full-length sequence of the gene of the V region comprising three CDRs and four FRs linked is amplified using primers that each anneal to the 5′ and 3′ ends thereof and have an added recognition sequence for an appropriate restriction enzyme. The DNA thus obtained and a human antibody C region-encoding DNA can be inserted into expression vectors such that these DNAs are fused in frame to prepare vectors for human-type antibody expression. These vectors having the inserts are transferred to hosts to establish recombinant cells. Then, the recombinant cells are cultured for the expression of the humanized antibody-encoding DNA to produce the humanized antibodies into the cultures of the cultured cells (See European Patent Publication EP239400 and International Publication WO1996002576).
The humanized antibodies thus prepared can be evaluated for their antigen-binding activity by qualitative or quantitative assay to thereby select suitable human antibody FRs that allow CDRs to form a favorable antigen-binding site when linked via the CDRs. If necessary, FR amino acid residue(s) may be substituted such that the CDRs of the resulting reshaped human antibody form an appropriate antigen-binding site. For example, the amino acid sequence of FR can be mutated by the application of the PCR method used in the mouse CDR grafting to the human FRs. Specifically, a mutation of a partial nucleotide sequence can be introduced to the primers annealing to a FR nucleotide sequence. The FR nucleotide sequence synthesized using such primers contains the mutation thus introduced. Such variant antibodies having the substituted amino acid(s) can be evaluated for their antigen-binding activity by the same assay as above to thereby select variant FR sequences having the desired properties (Cancer Res., (1993) 53, 851-856).
Furthermore, a desired human antibody can be obtained through DNA immunization using a transgenic animal having all repertories of a human antibody gene (see, International Publication WO1993/012227, WO1992/003918, WO1994/002602, WO1994/025585, WO1996/034096, WO1996/033735) as an immunized animal.
Moreover, a technique for obtaining a human antibody by panning using a human antibody library is also known in the art. For example, a human-antibody V region is expressed on the surface of a phage as a single-chain antibody (scFv) by a phage display method. A phage expressing a scFv binding to an antigen can be selected. A DNA sequence encoding a human antibody V region binding to the antigen can be determined by analyzing the gene of the selected phage. After the DNA sequence of the scFv binding to the antigen is determined, the V region sequence is fused with the sequence of a desired human antibody C region in frame and inserted into an appropriate expression vector. In this manner, the expression vector can be prepared. The expression vector is introduced in a preferable expression cell as mentioned above and a gene encoding the human antibody is allowed to express to obtain the human antibody. These methods are already known in the art (see, International Publication WO1992/001047, WO1992/020791, WO1993/006213, WO1993/011236, WO1993/019172, WO1995/001438, WO1995/015388).
As a method for obtaining an antibody gene, a B cell cloning method described in Bernasconi et al. (Science (2002) 298, 2199-2202) or described in WO2008/081008 (identification, cloning, isolation of individual antibody coding sequences and use thereof for constructing expression vectors for preparing individual antibodies (particularly, IgG1, IgG2, IgG3 or IgG4) etc.) can be appropriately used other than those mentioned above.
According to the method used in the present invention, amino acid positions assigned for CDR and FR of an antibody are defined in accordance with Kabat (Sequences of Proteins of Immunological Interest (National Institute of Health, Bethesda, Md., 1987 and 1991). In the specification, when an antigen-binding molecule is an antibody or an antigen binding fragment, the amino acids in a variable region are indicated in accordance with the Kabat numbering, whereas amino acids in a constant region are indicated by the EU numbering in accordance with the Kabat amino acid positions.
Unlike an Fcγ receptor belonging to an immunoglobulin superfamily, a human FcRn is structurally analogous to a polypeptide of a major histoincompatible complex (MHC) class I and has a sequence homology of 22 to 29% with class I MHC molecules (Ghetie et al., Immunol. Today (1997) 18 (12), 592-598). FcRn is expressed as a hetero dimer, which is a complex formed of soluble β chain or a light chain (β2 microglobulin) and a transmembrane a chain or a heavy chain. Like MHC, the α chain of FcRn consists of 3 extracellular domains (α1, α2, α3), and a short cytoplasmic domain plays a role of anchoring a protein on a cell surface. The α1 and α2 domains interact with an FcRn binding domain in the Fc region of an antibody (Raghavan et al. (Immunity (1994) 1, 303-315)).
FcRn is expressed in the placenta or yolk sac of a mammalian animal and involved in IgG transfer from a mother to a fetus. In addition, in the small intestine of a new-bone baby rodent in which FcRn is expressed, FcRn is involved in transferring a maternal IgG from ingested first milk or milk across through the brush border epithelium. FcRn is expressed in various tissues other than the aforementioned tissue and various endothelial cells in a wide variety of species. FcRn is also expressed in human adult vascular endothelial cells, muscular and blood vessel system and liver vasis sinusoideum. FcRn binds to IgG and recycles it to the serum. FcRn is thus considered to play a role in maintaining the concentration of IgG in plasma. FcRn binds to an IgG molecule usually definitely depending upon pH and optimal binding is observed in an acidic pH range of less than 7.0.
Human FcRn, which is obtained from a polypeptide containing a signal sequence represented by SEQ ID NO: 4 (FcRn; NP—004098.1) as a precursor (the polypeptide containing a signal sequence is described in SEQ ID NO: 5 (beta2-microglobulin; NP—004039.1)), forms a complex with human β2-microglobulin in-vivo. As shown in Examples later, a soluble human FcRn, which forms a complex with β2-microglobulin, is produced by use of a conventional recombinant expression method. The binding activity of the Fc region of the present invention to such soluble human FcRn (which forms a complex with (32-microglobulin) can be evaluated. In the present invention, unless otherwise specified, human FcRn refers to a human FcRn having a structure capable of binding to the Fc region of the present invention. Examples thereof include a complex of human FcRn and human β2-microglobulin.
The antigen-binding molecule of the present invention has an FcRn binding domain. The FcRn binding domain is not particularly limited as long as the antigen-binding molecule has a binding activity to FcRn in an acidic pH range. The FcRn binding domain may be a domain having an activity to directly or indirectly bind to FcRn. As such a domain, the Fc region of an IgG immunoglobulin having an activity to directly bind to FcRn, albumin, albumin domain 3, an anti-FcRn antibody, an anti-FcRn peptide and an anti-FcRn scaffold (Scaffold) molecule are preferably mentioned; or an IgG having an activity to indirectly bind to FcRn and a molecule binding to albumin are mentioned. In the present invention, a domain having a binding activity to FcRn in an acidic pH range and a neutral pH range is preferable. The domain, as long as it already has a binding activity to FcRn in an acidic pH range, can be preferably used as it is. When the domain has no binding activity or a weak binding activity to FcRn in an acidic pH range, it is possible to provide a binding activity to FcRn by modifying the amino acids of the antigen-binding molecule. Alternatively, the FcRn-binding activity may be enhanced by modifying the amino acids of the domain already having a binding activity to FcRn in an acidic pH range. In modifying the amino acids of the FcRn binding domain, a desired modification can be found out by comparing the binding activities to FcRn in an acidic pH range before and after amino acid modification.
The FcRn binding domain is preferably a region which directly binds to FcRn. As a preferable example of the FcRn binding domain, the Fc region of an antibody can be mentioned. However, a region, which can bind to a polypeptide having a binding activity to FcRn, such as albumin and IgG, can indirectly bind to FcRn via albumin or IgG, etc. Accordingly, as the FcRn binding region in the present invention, a region, which can bind to the polypeptide having a binding activity to FcRn, can be preferably used. The Fc region contains an amino acid sequence derived from a constant region of an antibody heavy chain. The Fc region is a portion of a heavy-chain constant region of an antibody ranging from the N terminal of a hinge region (papain cleavage portion) including the hinge, CH2 and CH3 domains and consisting of approximately 216 amino acids represented by the EU numbering.
In the present invention, the binding activity of the FcRn binding domain to FcRn (particularly human FcRn), can be measured by a method known to those skilled in the art, as described in the section of “Binding activity”. Conditions other than pH can be appropriately determined by those skilled in the art. The antigen-binding activity and human FcRn-binding activity of an antigen-binding molecule are evaluated based on e.g., KD (Dissociation constant), apparent KD (Apparent dissociation constant), kd (Dissociation rate) or apparent kd (Apparent dissociation rate). They can be measured by methods known to those skilled in the art such as Biacore (GE healthcare), Scatchard plot and flow cytometer.
In measuring the binding activity of an FcRn binding domain to FcRn, conditions other than pH can be appropriately determined by those skilled in the art and are not particularly limited. The binding activity can be measured in MES buffer at 37° C., as is described in WO2009/125825. In the present invention, the binding activity of an FcRn binding domain to FcRn can be measured by a method known to those skilled in the art, such as Biacore (GE Healthcare). The binding activity of an FcRn binding domain to FcRn can be measured and evaluated by feeding FcRn, or an FcRn binding domain or the antigen-binding molecule of the present invention containing an FcRn binding domain as an analyte, to chips on which an FcRn binding domain or the antigen-binding molecule of the present invention containing an FcRn binding domain or FcRn is immobilized.
The acidic pH range used as a condition, in which the binding activity of the FcRn binding domain contained in the antigen-binding molecule of the present invention to FcRn is obtained, usually refers to a region of pH 4.0 to pH 6.5, preferably pH 5.5 to pH 6.5, and particularly preferably, pH 5.8 to pH 6.0 which is close to pH value within the early-stage endosome in-vivo. The binding affinity of an FcRn binding domain for FcRn may be evaluated at any measurement temperature from 10° C. to 50° C. Preferably, the binding affinity of an FcRn binding domain for human FcRn is determined at a temperature of 15° C. to 40° C. More preferably, the binding affinity of an FcRn binding domain for FcRn is determined at any temperature from 20° C. to 35° C., such as 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, and 35° C. A temperature of 25° C. is a non-limiting example of the present invention.
According to Yeung et al. (J. Immunol. (2009) 182, 7663-7671), the binding activity of natural human IgG1 to human FcRn in an acidic pH range (pH 6.0) is KD 1.7 μM; however, the activity cannot be virtually detected in a neutral pH range. Accordingly, in a preferable aspect, it is possible to use the antigen-binding molecule of the present invention having a binding activity to human FcRn under the acidic pH range condition, which includes an antigen-binding molecule whose binding activity to human FcRn under an acidic pH range condition is KD 20 μM or stronger and whose binding activity to human FcRn under a neutral pH range condition is the same as that of a natural human IgG. In more preferable aspect, the antigen-binding molecule of the present invention including an antigen-binding molecule whose human FcRn-binding activity under the acidic pH range condition is KD 2.0 μM or stronger, can be used. In further more preferable aspect, an antigen-binding molecule whose human FcRn-binding activity under the acidic pH range condition is KD 0.5 μM or stronger can be used. The aforementioned KD value is determined in accordance with the method described in The Journal of Immunology (2009) 182: 7663-7671 (an antigen-binding molecule is immobilized to a chip, to which human FcRn is fed as an analyte).
In the present invention, an Fc region having a binding activity to FcRn under an acidic pH range condition is preferable. As the Fc domain, any Fc domain can be used if the domain is an Fc region already having a binding activity to FcRn under an acidic pH range condition, the domain can be used as it is. If the domain has no or weak binding activity to FcRn under an acidic pH range condition, an Fc region having a desired binding activity to FcRn can be obtained by modifying an amino acid in an antigen-binding molecule. Also, an Fc region having a desired or enhanced binding activity to FcRn under an acidic pH range condition can be preferably obtained by modifying an amino acid in the Fc region. The amino acid modification in an Fc region by which such a desired binding activity is brought, can be found by comparing binding activities to FcRn before and after modification of an amino acid under the acidic pH range condition. Those skilled in the art can appropriately modify an amino acid by use of a method known in the art as described in the section of “Modification of amino acid” in the specification.
The Fc region (contained in the antigen-binding molecule of the present invention) having a binding activity to FcRn under the acidic pH range condition, can be obtained by any method. To describe it more specifically, an FcRn binding domain having a binding activity to FcRn or an enhanced binding activity to FcRn under an acidic pH range condition can be obtained by modification of an amino acid of a human IgG immunoglobulin used as a starting Fc region. As a preferable Fc region of the IgG immunoglobulin to be modified, for example, the Fc region of a human IgG (IgG1, IgG2, IgG3, or IgG4, and a modified form of them) are mentioned. Other than these, an amino acid at any position can be modified as long as the binding activity to FcRn is obtained under an acidic pH range condition or the binding activity to human FcRn under the acidic pH range can be enhanced. If an antigen-binding molecule contains human IgG1 Fc region as an Fc region, it is preferable to contain a modification by which an effect of enhancing binding to FcRn under an acidic pH range condition is brought compared to the binding activity of a starting Fc region of human IgG1. Preferable examples of the amino acid that can be modified as mentioned above include amino acids (represented by the EU numbering) at position 238, position 252, position 253, position 254, position 255, position 256, position 265, position 272, position 286, position 288, position 303, position 305, position 307, position 309, position 311, position 312, position 317, position 340, position 356, position 360, position 362, position 376, position 378, position 380, position 382, position 386, position 388, position 400, position 413, position 415, position 424, position 433, position 434, position 435, position 436, position 439 and/or position 447 (as described in WO2000/042072). Similarly, preferable examples of such amino acid that can be modified as mentioned above amino acids (represented by the EU numbering) at position 251, position 252, position 254, position 255, position 256, position 308, position 309, position 311, position 312, position 385, position 386, position 387, position 389, position 428, position 433, position 434, and/or position 436 (described in WO2002/060919). Furthermore, preferable examples of such amino acid that can be modified as mentioned above include amino acids (represented by the EU numbering) at position 250, position 314, and position 428 (described in WO2004/092219). Moreover, preferable examples of such amino acid that can be modified as mentioned above include amino acids (represented by the EU numbering) at position 251, position 252, position 307, position 308, position 378, position 428, position 430, position 434, and/or position 436 (described in WO2010/045193). The binding of the Fc region of an IgG immunoglobulin to FcRn under an acidic pH range condition is enhanced by modification of these amino acids.
The Binding of the Fc region of IgG to FcRn under an acidic pH range condition can be enhanced by using, for example, these modifications of amino acids singly or in combination. The modification of amino acid to be introduced is not particularly limited, and any amino acid modification may be introduced as long as a plasma retentivity improving effect is produced.
According to a non-limiting aspect of the present invention, as an FcRn binding domain, an antigen-binding domain having a binding activity to FcRn, particularly human FcRn, can be also appropriately used. As described above, as the antigen-binding molecule of the present invention, a bispecific antibody can be appropriately used. Of them, a bispecific antibody recognizing two epitopes, one of which is present in a desired antigen except FcRn and the other of which is present in FcRn, is preferably mentioned. The structure of the bispecific antibody is not particularly limited to a specific structure as long as it contains a bivalent binding domain (binding to a desired antigen and FcRn) and a sugar chain receptor-binding domain. For example, a structure of an antibody such as an IgG antibody, in which Fc regions are linked, can be used. Besides, e.g., “scFv2 (single chain Fv 2)”, “diabody”, or “F(ab′)2” can be preferably used. When a structure of an antibody such as an IgG antibody is used, a sugar chain binding domain can be contained not only in an Fc region but also in an FcRn binding domain and/or an antigen-binding domain. Furthermore, when a structure of “scFv2 (single chain Fv 2)”, “diabody”, or “F(ab′)2” is used, a sugar chain binding domain can be also contained in an FcRn binding domain and/or an antigen-binding domain.
When such a bispecific antibody is used, as an FcRn binding domain, an FcRn binding domain, whose binding to FcRn changes depending upon the ion-concentration condition (as described later in the section of “Conditions of ion concentration”) can be appropriately used. More specifically, according to a non-limiting aspect of the present invention, an FcRn binding domain, whose binding to FcRn changes depending upon the condition of metal ion concentration and pH condition, can be used (as later described in the section of “Conditions of ion concentration”).
In a non-limiting aspect of the present invention, the ion concentration refers to a metal-ion concentration. The “metal ion” refers to an ion of a metal element belonging to Group I including alkali metals except hydrogen and coppers; Group II including alkali earth metals and zincs; Group III except boron; Group IV except carbon and silicon; Group VIII including iron and platinum; elements belonging to a sub A group of each of Group V, VI and VII, and metal elements such as antimony, bismuth and polonium. A metal atom is disposed to release an atomic electron(s) into a cation. This property is called ionization tendency. A metal having large ionization tendency is said to be chemically highly active.
In the present invention, a calcium ion is mentioned as a preferable example of such a metal ion. The calcium ion is involved in control of many life phenomena, more specifically involved in contraction of muscle such as skeleton muscle, smooth muscle and cardiac muscle, activation of movement and phagocytosis of leucocytes, activation of deformation and secretion of platelets, activation of lymphocytes, activation of mast cells such as secretion of histamine, cellular response via a catecholamine α receptor and an acetylcholine receptor, exocytosis, release of a transmittance from a neuron terminal and axonal flow of a neuron. As an intracellular calcium ion receptor, Troponin C, calmodulin, parvalbumin and myosin light-chain, etc. are known, which have a plurality of calcium ion-binding sites and are presumably derived from the same origin in view of molecular evolution. Many binding motifs of them are also known. For example, a cadherin domain, EF hand contained in calmodulin, a C2 domain contained in Protein kinase C, a Gla domain contained in blood coagulation protein, Factor IX, a C type lectin contained in an asialoglycoprotein receptor and a mannose receptor, an A domain contained in an LDL receptor, annexin, a thrombospondin type III domain and an EGF-like domain are known well.
In the present invention, when the metal ion is a calcium ion, as a calcium-ion concentration condition, the low calcium-ion concentration condition and a high calcium-ion concentration condition are mentioned. The expression: “the binding activity changes depending upon a calcium-ion concentration condition” means that the binding activity of an antigen-binding molecule to an antigen changes depending upon the difference in conditions between a low calcium-ion concentration and a high calcium-ion concentration. For example, a case where the binding activity of an antigen-binding molecule to an antigen is higher under a high calcium-ion concentration condition than the binding activity of the antigen-binding molecule to the antigen under a low calcium-ion concentration condition, is mentioned. Alternatively, a case where the binding activity of an antigen-binding molecule to an antigen under a low calcium-ion concentration condition is higher than (the binding activity of the antigen-binding molecule to the antigen) under a high calcium-ion concentration condition, is mentioned.
In the specification, the high calcium-ion concentration is not limited to a single numerical value and can be preferably a concentration selected from the range between 100 μM to 10 mM. In another aspect, the high calcium-ion concentration can be a concentration selected from the range between 200 μM to 5 mM. In another aspect, the high calcium-ion concentration can be a concentration selected from the range between 500 μM to 2.5 mM, and in another aspect, from 200 μM to 2 mM, and further from 400 μM to 1.5 mM. In particular, a concentration selected from the range between 500 μM to 2.5 mM, which is close to the calcium-ion concentration of in-vivo plasma (in blood), is preferably mentioned.
In the specification, the low calcium-ion concentration is not limited to a single numerical value and can be preferably a concentration selected from the range between 0.1 μM to 30 μM. In another aspect, the low calcium-ion concentration can be a concentration selected from the range between 0.2 μM to 20 μM. In another aspect, the low calcium-ion concentration can be a concentration selected from the range between from 0.5 μM to 10 μM, and in another aspect, from 1 μM to 5 μM, and further from 2 μM to 4 μM. In particular, a concentration selected from the range between 1 μM to 5 μM, which is close to the calcium-ion concentration of an early-stage endosome in vivo, is preferably mentioned.
In the present invention, the expression: the binding activity to an antigen under a low calcium-ion concentration condition is lower than the binding activity to the antigen under a high calcium-ion concentration condition, means that the binding activity of an antigen-binding molecule to an antigen in a calcium-ion concentration selected from the range between 0.1 μM to 30 μM is weaker than the binding activity to the antigen in a calcium-ion concentration selected from the range between 100 μM to 10 mM. Preferably, the binding activity of an antigen-binding molecule to an antigen in a calcium-ion concentration selected from the range between 0.5 μM to 10 μM is weaker than (the binding activity of the antigen-binding molecule to the antigen) in a calcium-ion concentration selected from the range between 200 μM to 5 mM. Particularly preferably, the antigen-binding activity in a calcium-ion concentration within the early-stage endosome in vivo is weaker than (the antigen-binding activity) in a calcium-ion concentration within plasma in-vivo. More specifically, the binding activity of an antigen-binding molecule to an antigen in a calcium-ion concentration selected from the range between 1 μM to 5 μM is weaker than the binding activity to the antigen in a calcium-ion concentration selected from the range between 500 μM to 2.5 mM.
Whether the binding activity of the antigen-binding domain of the present invention to an antigen changes or not depending upon the metal ion-concentration condition can be determined by use of a measurement method known in the art (as described, for example, in the above section of “Binding activity”). For example, to determine that the binding activity of an antigen-binding molecule containing the antigen-binding domain of the present invention to an antigen under a high calcium-ion concentration condition changes in a higher level than the binding activity of the antigen-binding molecule containing the antigen-binding domain to the antigen under a low calcium-ion concentration condition, the binding activity of the antigen-binding molecule containing the antigen-binding domain to an antigen is compared between under the low calcium-ion concentration condition and under a high calcium-ion concentration condition.
In the present invention, the expression: “the binding activity to an antigen under the low calcium-ion concentration condition is lower than the binding activity to the antigen under a high calcium-ion concentration condition” can be rephrased by the expression that the binding activity of an antigen-binding molecule to an antigen under a high calcium-ion concentration condition is higher than the binding activity to the antigen under a low calcium-ion concentration condition. Note that, in the present invention “the binding activity to an antigen under a low calcium-ion concentration condition is lower than the binding activity to the antigen under a high calcium-ion concentration condition” is sometimes described as “the binding ability to an antigen under a low calcium-ion concentration condition is weaker than the binding ability to the antigen under a high calcium-ion concentration condition”; and “the antigen-binding activity to an antigen under a low calcium-ion concentration condition is lowered than the antigen-binding activity under a high calcium-ion concentration condition” is sometimes described as “the binding ability to an antigen under a low calcium-ion concentration condition is weaken than the antigen binding ability under a high calcium-ion concentration condition”.
Conditions for measuring the binding activity to an antigen other than the calcium-ion concentration can be appropriately selected by those skilled in the art and are not particularly limited. For example, measurement can be performed in a HEPES buffer at 37° C. For example, measurement can be performed by use of Biacore (GE Healthcare), etc. The binding activity of an antigen-binding molecule containing an antigen-binding domain to an antigen, in the case the antigen is a soluble antigen, can be measured and evaluated by feeding the antigen-binding molecule containing an antigen-binding domain as an analyte to a chip having the antigen immobilized thereto. If the antigen is a membrane antigen, the binding activity to the membrane antigen can be evaluated by feeding the antigen-binding molecule containing an antigen-binding domain as an analyte to a chip having the antigen immobilized thereto.
In the antigen-binding molecule of the present invention, as long as the binding activity to an antigen in a low calcium-ion concentration condition is weaker than the binding activity to the antigen in a high calcium-ion concentration condition, the ratio of the binding activity to the antigen under the low calcium-ion concentration condition relative to the binding activity to the antigen under the high calcium-ion concentration condition is not particularly limited; however, the ratio is expressed by the ratio of KD (Dissociation constant) of the antigen in the low calcium-ion concentration condition relative to KD in the high calcium-ion concentration condition, i.e., a value of KD (Ca 3 μM)/KD (Ca 2 mM). This value (KD (Ca 3 μM)/KD (Ca 2 mM)) is preferably 2 or more, more preferably 10 or more and further preferably is 40 or more. The upper limit of the value of KD ((Ca 3 μM)/KD (Ca 2 mM)) is not particularly limited as long as preparation can be made by technique of those skilled in the art. Any value such as 400, 1000, 10000 can be employed. Furthermore, the ratio can be specified by a value of KD (Ca3 μM)/KD (Ca 1.2 mM). The value of KD (Ca 3 μM)/KD (Ca 1.2 mM) is 2 or more, more preferably 10 or more and further preferably 40 or more. The upper limit of the value of KD (Ca 3 μM)/KD (Ca 1.2 mM) is not particularly limited. As long as preparation can be made by technique of those skilled in the art, any value such as 400, 1000, 10000 can be employed.
As a value showing the binding activity to an antigen, KD (dissociation constant) can be used if the antigen is a soluble antigen; however, if the antigen is a membrane antigen, an apparent KD (Apparent dissociation constant) can be used. The KD (dissociation constant) and apparent KD (apparent dissociation constant) can be determined by a method known to those skilled in the art, for example, determined by use of Biacore (GE healthcare), Scatchard plot and a flow cytometer.
Furthermore, as another index showing the ratio of the binding activity of the antigen-binding molecule of the present invention to an antigen in a low-calcium concentration condition relative to the binding activity in a high-calcium concentration condition, for example, a dissociation rate constant, i.e., kd (Dissociation rate constant), is further preferably used. When kd (dissociation rate constant) is used in place of KD (dissociation constant) as the index showing the ratio of the binding activity, the ratio of kd (dissociation rate constant) in a low-calcium concentration condition to an antigen relative to kd (dissociation rate constant) in a high-calcium concentration condition, i.e., a value of kd (low-calcium concentration condition)/kd (high-calcium concentration condition), is preferably 2 or more, more preferably 5 or more, further preferably 10 or more and still more preferably 30 or more. The upper limit of the value of kd (low-calcium concentration condition)/kd (high-calcium concentration condition) is not particularly limited. As long as preparation can be made by common technical knowledge of those skilled in the art, any value such as 50, 100 and 200 may be used.
As the value of an antigen-binding activity, kd (dissociation rate constant) can be used if the antigen is a soluble antigen; however, if the antigen is a membrane antigen, an apparent kd (Apparent dissociation rate constant) can be used. The kd (dissociation rate constant) and apparent kd (apparent dissociation rate constant) can be measured by a method known to those skilled in the art, such as Biacore (GE healthcare), Scatchard plot and a flow cytometer. Note that, in the present invention, when the binding activity of an antigen-binding molecule to an antigen is measured in different calcium-ion concentrations, conditions other than the calcium concentrations are preferably the same.
For example, according to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, can be obtained by a screening for the antigen-binding domain or the antibody comprising the following steps (a) to (c):
(a) a step of obtaining the antigen-binding activity of each of antigen-binding domains or antibodies in a low-calcium concentration condition,
(b) a step of obtaining the antigen-binding activity of each of the antigen-binding domains or antibodies in a high-calcium concentration condition, and
(c) a step of selecting an antigen-binding domain or antibody having a lower antigen-binding activity in the condition of the low-calcium concentration condition than (the antigen-binding activity) in the high-calcium concentration condition.
According to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, can be obtained by a screening for the antigen-binding domain, the antibody or libraries of these comprising the following steps (a) to (c):
(a) a step of bringing antigen-binding domains, antibodies or libraries of them into contact with an antigen in a high-calcium concentration condition,
(b) a step of placing the antigen-binding domains or antibodies that bind to the antigen in the step (a), under a low-calcium concentration condition, and
(c) a step of isolating an antigen-binding domain or antibody that dissociates in the step (b).
According to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition can be obtained by a screening for the antigen-binding domain or antibody or libraries of them comprising the following steps (a) to (d):
(a) a step of bringing antigen-binding domains or an antibody library into contact with an antigen in a low-calcium concentration condition,
(b) a step of selecting the antigen-binding domain or antibody that does not bind to the antigen in the step (a),
(c) a step of binding the antigen-binding domain or antibody selected in the step (b) to the antigen under a high-calcium concentration condition, and
(d) a step of isolating the antigen-binding domain or antibody that binds to the antigen in the step (c).
According to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, can be obtained by a screening process comprising the following steps (a) to (c):
(a) a step of bringing antigen-binding domains or an antibody library into contact with a column having the antigen immobilized thereto in a high-calcium concentration condition,
(b) a step of releasing the antigen-binding domain or antibody that binds to the column in the step (a) by elution from the column in a low-calcium concentration condition, and
(c) a step of isolating the antigen-binding domain or antibody released by elution in the step (b).
According to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, can be obtained by a screening process comprising the following steps (a) to (d):
(a) a step of passing antigen-binding domains or an antibody library through a column having an antigen immobilized thereto, in a low-calcium concentration condition,
(b) a step of recovering the antigen-binding domain or antibody that is released by elution without binding to the column in the step (a),
(c) a step of binding the antigen-binding domain or antibody recovered in the step (b) to the antigen in a high-calcium concentration condition, and
(d) a step of isolating the antigen-binding domain or antibody that binds to the antigen in the step (c).
According to an aspect of the present invention, an antigen-binding domain or antibody whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, can be obtained by a screening process comprising the following steps (a) to (d):
(a) a step of bringing antigen-binding domains or an antibody library into contact with an antigen in a high-calcium concentration condition,
(b) a step of obtaining antigen-binding domains or antibodies that bind to the antigen in the step (a),
(c) a step of placing the antigen-binding domain or antibody obtained in the step (b) under a low-calcium concentration condition, and
(d) a step of isolating the antigen-binding domain or antibody whose antigen-binding activity in the step (c) is weaker than the standard selected in the step (b).
Note that the aforementioned steps may be repeated twice or more. Thus, according to the present invention, an antigen-binding domain or antibody, whose binding activity to an antigen in a low calcium-ion concentration condition is lower than the binding activity to the antigen in a high calcium-ion concentration condition, obtained by any one of the aforementioned screening processes further comprising a step of repeating the steps (a) to (c) or (a) to (d), twice or more, is provided. The number of repeats of (a) to (c) or (a) to (d) steps is not particularly limited; however, the number of repeats is usually within 10 times.
In the screening method of the present invention, the antigen-binding activity of an antigen-binding domain or an antibody in a low-calcium concentration condition is not particularly limited, as long as it is the antigen-binding activity obtained at a calcium-ion concentration between 0.1 μM and 30 μM. The antigen-binding activity obtained at a more preferable calcium-ion concentration between 0.5 μM and 10 μM is mentioned. As a more preferable calcium-ion concentration, a calcium-ion concentration within early-stage endosome in vivo is mentioned. More specifically, the antigen-binding activity obtained at a calcium-ion concentration of 1 μM to 5 μM can be mentioned. In contrast, the antigen-binding activity of an antigen-binding domain or an antibody under a high-calcium concentration condition is not particularly limited, as long as it is the antigen-binding activity obtained at a calcium-ion concentration between 100 μM and 10 mM. The antigen-binding activity obtained at a preferable calcium-ion concentration between 200 μM and 5 mM is mentioned. As a more preferable calcium-ion concentration, a calcium-ion concentration within plasma in-vivo can be mentioned. More specifically, the antigen-binding activity obtained at a calcium-ion concentration of 0.5 mM to 2.5 mM can be mentioned.
The binding activity of an antigen-binding domain or an antibody can be measured by a method known to those skilled in the art. Conditions other than a calcium-ion concentration can be appropriately determined by those skilled in the art. The antigen-binding activity of an antigen-binding domain or an antibody can be evaluated based on e.g., KD (Dissociation constant), apparent KD (Apparent dissociation constant), a dissociation rate, kd (Dissociation rate) or apparent kd (Apparent dissociation). These can be measured by a method known to those skilled in the art such as Biacore (GE healthcare), Scatchard plot, FACS.
In the present invention, the step of selecting an antigen-binding domain or antibody, whose antigen-binding activity under a high-calcium concentration condition is higher than (the antigen-binding activity) under a low-calcium concentration condition, is equivalent to a step of selecting an antigen-binding domain or antibody whose antigen-binding activity under a low-calcium concentration condition is lower than (the antigen-binding activity) under a high-calcium concentration condition.
As long as the antigen-binding activity under a high-calcium concentration condition is higher than (the antigen-binding activity) under a low-calcium concentration condition, difference between the antigen-binding activity under a high-calcium concentration condition and the antigen-binding activity under a low-calcium concentration condition is not particularly limited; however, the antigen-binding activity under a high-calcium concentration condition is preferably twice or more as high as the antigen-binding activity under a low-calcium concentration condition, more preferably, 10 fold or more and further preferably 40 fold or more.
The antigen-binding domain or antibody of the present invention to be screened by any one of the screening methods mentioned above is not particularly limited. For example, any one of the aforementioned antigen-binding domains or antibodies can be screened. For example, an antigen-binding domain or an antibody having a natural sequence can be screened or an antigen-binding domain or antibody whose amino acid sequence is substituted, may be screened.
(2) Amino Acid that Changes the Binding Activity of Antigen-Binding Domain to Antigen Depending Upon the Calcium-Ion Concentration Condition
The antigen-binding domain or antibody of the present invention to be screened by any one of the screening methods as mentioned above may be prepared in any manner. For example, if a metal ion is a calcium ion, antibodies already exist; libraries (phage library, etc.) already exist; antibodies or libraries prepared from hybridomas prepared by immunization of animals or the B cells of immunized animals; and antibodies or libraries prepared by introducing an amino acid (e.g., aspartic acid and glutamine acid) capable of chelating calcium and a non-natural amino acid mutation into these antibodies, (a library prepared by introducing an amino acid (e.g., aspartic acid and glutamine acid) capable of chelating calcium, a library whose non-natural amino acid content is increased or a library prepared by introducing an amino acid (e.g., aspartic acid and glutamine acid) capable of chelating calcium or a non-natural amino acid mutation into a specific site), can be used.
As the amino acid that changes the binding activity of an antigen-binding molecule to an antigen depending upon the ion-concentration condition as described above, if a metal ion is a calcium ion, as long as it is an amino acid forming a calcium-binding motif, the type of amino acid is not limited. The calcium-binding motifs are known to those skilled in the art and more specifically described in the literatures: (for example, Springer et al. (Cell (2000) 102, 275-277), Kawasaki and Kretsinger (Protein Prof. (1995) 2, 305-490), Moncrief, et al. (J. Mol. Evol. (1990) 30, 522-562), Chauvaux, et al. (Biochem. J. (1990) 265, 261-265), Bairoch and Cox (FEBS Lett. (1990) 269, 454-456), Davis (New Biol. (1990) 2, 410-419), Schaefer, et al. (Genomics (1995) 25, 638 to 643), Economou, et al. (EMBO J. (1990) 9, 349-354), Wurzburg, et al. (Structure. (2006) 14, 6, 1049-1058)). More specifically, any known calcium-binding motifs such as C type lectins including ASGPR, CD23, MBR and DC-SIGN can be contained in the antigen-binding molecule of the present invention. As a preferable example of such a calcium-binding motif other than the aforementioned ones, a calcium-binding motif contained in the antigen-binding domain represented by SEQ ID NO: 6 can be mentioned.
As the amino acid that changes the binding activity of an antigen-binding molecule to an antigen depending upon the calcium-ion concentration condition, an amino acid having a metal chelating function is also preferably used. Preferable examples of the amino acid having a metal chelating function include serine (Ser (S)), threonine (Thr (T)), asparagine (Asn (N)), glutamine (Gln (Q)), aspartic acid (Asp (D)) and glutamine acid (Glu (E)).
The position of the antigen-binding domain containing an amino acid is not particularly limited to a specific position. As long as the binding activity of an antigen-binding molecule to an antigen is changed depending upon the calcium-ion concentration condition, any position in a heavy-chain variable region or a light-chain variable region forming the antigen-binding domain may be acceptable. More specifically, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing an amino acid that changes the binding activity of an antigen-binding molecule to an antigen depending upon the calcium-ion concentration condition in a heavy chain antigen-binding domain. According to another non-limiting aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid in a heavy chain CDR3. According to another non-limiting aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid in heavy chain CDR3 at the position 95, position 96, position 100a, and/or position 101 (represented by Kabat numbering).
In a non-limiting aspect of the present invention, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing an amino acid that changes the binding activity of an antigen-binding molecule to an antigen depending upon the calcium-ion concentration condition, in a light chain antigen-binding domain. In another aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid in light chain CDR1. In another aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid in light chain CDR1 at the position 30, position 31, and/or position 32 (represented by Kabat numbering).
In another non-limiting aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in light chain CDR2. In another aspect, a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in light chain CDR2, at the position 50 (represented by Kabat numbering) is provided.
In another non-limiting aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in light chain CDR3. In another aspect, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in light chain CDR3 at the position 92 (represented by Kabat numbering).
The antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in a 2 or 3 CDRs selected from light chain CDR1, CDR2 and CDR3 mentioned above, as a different aspect of the present invention. Furthermore, the antigen-binding domain of the present invention can be obtained from a library mainly consisting of antigen-binding molecules mutually different in sequence and containing the amino acid residue in a light chain at at least one position of the position 30, position 31, position 32, position 50, and/or position 92 (represented by Kabat numbering).
As long as these amino acid residues form a calcium-binding motif and/or as long as the binding activity of an antigen-binding molecule to an antigen changes depending upon the calcium-ion concentration condition, these amino acid residues can be contained alone and in combination of two or more. Furthermore, troponin C, calmodulin, parvalbumin and myosin light-chain, etc., which have a plurality of calcium ion-binding sites and are presumably derived from the same origin in view of molecular evolution, are known and light chain CDR1, CDR2 and/or CDR3 can be designed so as to contain its binding motif(s). For example, a cadherin domain, EF hand contained in calmodulin, a C2 domain contained in Protein kinase C, a Gla domain contained in a blood coagulation protein, Factor IX, a C type lectin contained in an asialoglycoprotein receptor and a mannose receptor, an A domain contained in an LDL receptor, Annexin, thrombospondin type III domain and EGF-like domain are appropriately used for the purpose described above.
In one aspect of the present invention, the antigen-binding domain of the present invention can be obtained from a library containing a plurality of antigen-binding molecules of the present invention having mutual different sequences and obtained by using a heavy-chain variable region (which is selected as a framework sequence already containing “at least one amino acid residue that changes the binding activity of an antigen-binding molecule to an antigen depending upon the ion-concentration condition”) in combination with a light-chain variable region (which is prepared as a randomized variable region sequence library). As a non-limiting example thereof, in the case where the ion concentration is a calcium-ion concentration, a library, which is obtained by using a heavy-chain variable region sequence represented by, for example, SEQ ID NO: 7 (6RL#9-IgG1) or SEQ ID NO: 8 (6KC4-1#85-IgG1) in combination with a light-chain variable region prepared as a randomized variable region sequence library is preferably mentioned. A library can be also prepared by appropriately selecting a light-chain variable region from the light-chain variable regions having a genital cell lineage sequence in place of the light-chain variable region prepared as the randomized variable region sequence library. For example, a library obtained by using the heavy-chain variable region sequence represented by SEQ ID NO: 7 (6RL#9-IgG1) or SEQ ID NO: 8 (6KC4-1#85-IgG1) in combination with a light-chain variable region having a genital cell lineage sequence is preferably mentioned.
In the specification, the “library” refers to a plurality of antigen-binding molecules or a plurality of fusion polypeptides each containing an antigen-binding molecule or nucleic acids and polynucleotides encoding these sequences. The sequences of the antigen-binding molecules or the fusion polypeptides each containing an antigen-binding molecule contained in the library are not the same and mutually different. In the library, a method for exposing a fusion polypeptide containing an antibody fragment on the surface of a bacteriophage is known in the art and described, for example, in WO1992001047 and this specification. Other than these, relevant methods are described in WO1992020791, WO1993006213, WO1993011236 and 1993019172. Those skilled in the art can appropriately use these methods. Other documents (H. R. Hoogenboom & G. Winter (1992) J. Mol. Biol. 227, 381-388, WO1993006213 and WO1993011236) disclose identification of antibodies against various antigens exposed on a phage surface by a variable region gene repertory artificially rearranged.
In one aspect of the present invention, the ion-concentration condition refers to a hydrogen ion-concentration condition or a pH condition. In the present invention, the concentration condition of an atomic nucleus of a proton, i.e., a hydrogen atom, is regarded as the same as the condition of hydrogen index (pH). If the active mass of a hydrogen ion in an aqueous solution is represented by aH+, pH is defined as −log 10aH+. If the ion intensity of the aqueous solution is low (for example, lower than 10−3), aH+ is almost equal to hydrogen ion intensity. For example, since the ionic product of water at 25° C. under 1 atmospheric pressure, Kw=aH+aOH=10-14, the ionic product in pure water is aH+=aOH=10-7. In this case, pH=7 is neutral. The aqueous solution having a pH value smaller than 7 is acidic; whereas, the aqueous solution having a pH value larger than 7 is alkaline.
In the present invention, when a pH condition is used as the ion-concentration condition, high hydrogen-ion concentration or low pH, i.e., an acidic pH range condition; a low hydrogen-ion concentration or higher pH, i.e., an neutral pH range condition are used as the pH condition. The expression: “binding activity changes depending upon the pH condition” means that the binding activity of an antigen-binding molecule to an antigen changes depending upon difference in condition, more specifically difference between a high hydrogen-ion concentration or low pH (an acidic pH range condition) and a low hydrogen-ion concentration or high pH (neutral pH range condition). For example, a case where the binding activity of an antigen-binding molecule to an antigen in a neutral pH range condition is higher than (the binding activity of the antigen-binding molecule to the antigen) in an acidic pH range condition, is mentioned. Another case where the binding activity of an antigen-binding molecule to an antigen in an acidic pH range condition is higher than (the binding activity of the antigen-binding molecule to the antigen) in a neutral pH range condition, is also mentioned.
In the specification, the neutral pH range, which is not limited to a single numerical value, can be selected preferably from pH 6.7 to pH 10.0, and selected from pH 6.7 to pH 9.5 in another aspect, pH 7.0 to pH 9.0 in another aspect, and pH 7.0 to pH 8.0 in another aspect. Particularly, pH 7.4, which is close to pH of plasma (in blood) in-vivo, is preferably mentioned.
In the specification, the acidic pH range, which is not limited to a single numerical value, can be selected preferably from pH 4.0 to pH 6.5, and selected from pH 4.5 to pH 6.5 in another aspect, pH 5.0 to pH 6.5 in another aspect, and pH 5.5 to pH 6.5 in another aspect. Particularly, pH 5.8, which is close to pH of calcium-ion concentration within early-stage endosome in-vivo, is preferably mentioned.
In the present invention, the expression: the binding activity of an antigen-binding molecule to an antigen in a high hydrogen-ion concentration condition or low pH (acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition or high pH (a neutral pH range), means that the binding activity of an antigen-binding molecule to an antigen at a pH selected from pH 4.0 to pH 6.5 is weaker than the binding activity to the antigen at a pH selected from pH 6.7 to pH 10.0; preferably, means that the binding activity of an antigen-binding molecule to an antigen at a pH selected from pH 4.5 to pH 6.5 is weaker than the binding activity to the antigen at a pH selected from pH 6.7 to pH 9.5; more preferably, means that the binding activity of an antigen-binding molecule to an antigen at a pH selected from pH 5.0 to pH 6.5 is weaker than the binding activity to the antigen at a pH selected from pH 7.0 to pH 9.0; further preferably means that the binding activity of an antigen-binding molecule to an antigen at a pH selected from pH 5.5 to pH 6.5 is weaker than (the binding activity to an antigen) at a pH selected from pH 7.0 to pH 8.0; particularly preferably means that antigen-binding activity at pH within early-stage endosome in-vivo is weaker than (the antigen-binding activity) at pH within plasma in-vivo; and, to be more specific, means that the binding activity of an antigen-binding molecule to an antigen at pH 5.8 is weaker than the binding activity to the antigen at pH 7.4.
Whether the binding activity of the antigen-binding domain of the present invention to an antigen changes or not depending upon the pH condition, can be determined by use of a measurement method known in the art as described, for example, in the above section “Binding activity”. To explain this more specifically, in the measurement method, the binding activity is measured in different pH conditions. For example, to confirm that the binding activity of an antigen-binding molecule containing the antigen-binding domain of the present invention to an antigen under a neutral pH range condition changes in a higher level than (the binding activity of the antigen-binding molecule containing the antigen-binding domain of the present invention) to the antigen under an acidic pH range condition, the binding activity of the antigen-binding molecule to the antigen under the acidic pH range condition is compared to that under the neutral pH range condition.
In the present invention, the expression: “the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)” can be expressed by the expression “the binding activity to an antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is higher than the binding activity to the antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range)”. Note that, in the present invention, “the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)” can be sometimes expressed by the expression: “the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is weaker than (the binding capacity to the antigen) in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)”; or the expression: “the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), is lowered than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)” is sometimes expressed by “the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), is weakened than (the binding activity to the antigen) in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range).
Conditions other than the hydrogen-ion concentration or pH in measuring the binding activity to an antigen can be appropriately selected by those skilled in the art and are not particularly limited. For example, measurement can be made in HEPES buffer at 37° C. and for example by use of Biacore (GE Healthcare), etc. The binding activity of an antigen-binding molecule containing an antigen-binding domain to an antigen, if the antigen is a soluble antigen, can be measured and evaluated by feeding the antigen as an analyte to a chip in which the antigen-binding molecule containing an antigen-binding domain is immobilized. If the antigen is a membrane antigen, the binding activity to the membrane antigen can be evaluated by feeding an antigen-binding molecule containing an antigen-binding domain as an analyte to a chip in which the antigen is immobilized.
In the antigen-binding molecule of the present invention, as long as the binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is weaker than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), the ratio of the binding activity to the antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) relative to the binding activity to an antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is not particularly limited; however, preferably, a KD (pH 5.8)/KD (pH 7.4) value (which is a ratio of KD in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) relative to KD in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)) is 2 or more; more preferably 10 or more and further preferably 40 or more. The upper limit of the value of KD (pH 5.8)/KD (pH 7.4) value is not particularly limited. As long as preparation can be made by technique of those skilled in the art, any value such as 400, 1000 and 10000 can be employed.
As the value of the binding activity to an antigen, if the antigen is a soluble antigen, KD (dissociation constant) can be used; however, if the antigen is a membrane antigen, an apparent KD (Apparent dissociation constant) can be used. The KD (dissociation constant) and apparent KD (apparent dissociation constant) can be determined by a method known to those skilled in the art, for example, by use of Biacore (GE healthcare), Scatchard plot and a flow cytometer.
As another index showing the ratio of the binding activity to the antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) relative to the binding activity to an antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), for example, a dissociation rate constant kd (Dissociation rate constant) can be further preferably used. When kd (dissociation rate constant) is used in place of KD (dissociation constant) as an index showing the ratio of the binding activity, a value of kd (acidic pH range)/kd (a neutral pH range) (which is the ratio of kd (dissociation rate constant) in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) relative to kd (dissociation rate constant) in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range)) is preferably 2 or more, more preferably 5 or more, further preferably 10 or more and still more preferably 30 or more. The upper limit of the value of kd (acidic pH range)/kd (a neutral pH range) is not particularly limited. As long as preparation can be made based on common technical knowledge of those skilled in the art, any value such as 50, 100 and 200 can be employed.
As the value of an antigen-binding activity, kd (dissociation rate constant) can be used if the antigen is a soluble antigen; however, if the antigen is a membrane antigen, an apparent kd (Apparent dissociation rate constant) can be used. The kd (dissociation rate constant) and apparent kd (apparent dissociation rate constant) can be determined by a method known to those skilled in the art, for example, by use of Biacore (GE healthcare) and a flow cytometer. Note that, in the present invention, when the binding activity of an antigen-binding molecule to an antigen is measured in different hydrogen-ion concentrations (i.e., pH), conditions other than the hydrogen-ion concentration (i.e., pH) are preferably the same.
For example, according to an aspect of the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening for the antigen-binding domain or the antibody, comprising the following steps (a) to (c):
(a) a step of obtaining the antigen-binding activity of each of antigen-binding domains or antibodies in an acidic pH-range condition,
(b) a step of obtaining the antigen-binding activity of each of the antigen-binding domains or antibodies in a neutral pH range condition, and
(c) a step of selecting an antigen-binding domain or antibody having a lower antigen-binding activity in the acidic pH-range condition than (the antigen-binding activity) in the neutral pH range condition.
According to an aspect of the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening process for the antigen-binding domain, the antibody or a library thereof, comprising the following steps (a) to (c):
(a) a step of bringing antigen-binding domains, antibodies or a library thereof into contact with an antigen in a neutral pH range condition,
(b) a step of placing the antigen-binding domains or antibodies that bind to the antigen in the step (a) under an acidic pH range condition, and
(c) a step of isolating the antigen-binding domain or antibody that dissociates in the step (b).
According to an aspect of the present invention, an antigen-binding domain or antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening for the antigen-binding domain or antibody or a library thereof, comprising the following steps (a) to (d):
(a) a step of bringing antigen-binding domains or an antibody library into contact with an antigen in an acidic pH-range condition,
(b) a step of selecting the antigen-binding domain or antibody that does not bind to the antigen in the step (a),
(c) a step of binding the antigen-binding domain or antibody selected in the step (b) to the antigen in a neutral pH range condition, and
(d) a step of isolating the antigen-binding domain or antibody that binds to the antigen in the step (c).
According to an aspect of the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening process, comprising the following steps (a) to (c):
(a) a step of bringing antigen-binding domains or an antibody library into contact with a column having the antigen immobilized thereto in a neutral pH range condition,
(b) a step of releasing the antigen-binding domain or antibody that binds to the column in the step (a) by elution from the column in the acidic pH range, and
(c) a step of isolating the antigen-binding domain or antibody released by elution in the step (b).
According to an aspect of the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening process, comprising the following steps (a) to (d):
(a) a step of passing antigen-binding domains or an antibody library through a column having an antigen immobilized thereto in an acidic pH range condition,
(b) a step of recovering the antigen-binding domain or antibody that is released by elution without binding to the column in the step (a), and
(c) a step of binding the antigen-binding domain or antibody recovered in the step (b) to the antigen in a neutral pH range condition, and
(d) a step of isolating the antigen-binding domain or antibody bound to the antigen in the step (c).
According to an aspect of the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than the binding activity to the antigen in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range), can be obtained by a screening process, comprising the following steps (a) to (d):
(a) a step of bringing antigen-binding domains or an antibody library into contact with an antigen in a neutral pH range condition,
(b) a step of obtaining the antigen-binding domains or antibodies that bind to the antigen in the step (a),
(c) a step of placing the antigen-binding domain or antibody obtained in the step (b) under the acidic pH range condition, and
(d) a step of isolating the antigen-binding domain or antibody whose antigen-binding activity in the step (c) is weaker than the standard selected in the step (b).
Note that the aforementioned steps may be repeated twice or more. Thus, according to the present invention, an antigen-binding domain or an antibody, whose binding activity to an antigen in an acidic pH-range condition is lower than the binding activity to the antigen in a neutral pH range condition, obtained by any one of the aforementioned screening processes further comprising a step of repeating the steps (a) to (c) or (a) to (d), twice or more is provided. The number of repeats of (a) to (c) or (a) to (d) steps is not particularly limited; however, the number of repeats is usually within 10 times.
In the screening method of the present invention, the binding activity of an antigen-binding domain or an antibody in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), is not particularly limited, as long as the antigen-binding activity is obtained in the pH range between 4.0 to 6.5, and preferably 4.5 to 6.6, still preferably 5.0 to 6.5, further preferably, 5.5 to 6.5, more preferably the pH of early-stage endosome in-vivo, more specifically, pH 5.8. Furthermore, the binding activity of an antigen-binding domain or an antibody in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is not particularly limited, as long as the antigen-binding activity is obtained in the pH range between 6.7 to 10, and preferably 6.7 to 9.5, still preferably 7.0 to 9.5, further preferably, 7.0 to 8.0, more preferably the pH of plasma in-vivo, more specifically, pH 7.4.
The binding activity of an antigen-binding domain or an antibody can be measured by a method known to those skilled in the art. Conditions other than a calcium-ion concentration can be appropriately determined by those skilled in the art. The binding activity of an antigen-binding domain or an antibody can be evaluated based on KD (Dissociation constant), apparent KD (Apparent dissociation constant), a dissociation rate, kd (Dissociation rate) or apparent kd (Apparent dissociation). These can be measured by a method known to those skilled in the art such as Biacore (GE healthcare), Scatchard plot, FACS, etc.
In the present invention, the step of selecting an antigen-binding domain or antibody whose antigen-binding activity in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is higher than (the antigen-binding activity) in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is equivalent to a step of selecting an antigen-binding domain or antibody whose antigen-binding activity in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range) is lower than (the antigen-binding activity) in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range).
As long as the antigen-binding activity in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is higher than (the antigen-binding activity) in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), difference between the antigen-binding activity in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) and the antigen-binding activity in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), is not particularly limited; however, preferably the antigen-binding activity in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) is twice or more as high as the antigen-binding activity in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), more preferably, 10 times or more, and further preferably 40 times or more.
The antigen-binding domain or antibody of the present invention to be screened by the screening method is not particularly limited. For example, the aforementioned antigen-binding domains or antibodies can be screened. For example, antigen-binding domains or antibodies having a natural sequence can be screened. Alternatively, antigen-binding domains or antibodies whose amino acid sequence is substituted may be screened.
The antigen-binding domain or antibody of the present invention to be screened by any one of the screening method mentioned above may be prepared in any manner. For example, antibodies already exist; libraries (phage library, etc.) already exist; antibodies or libraries prepared from hybridomas (prepared by immunization of animals) or the B cells of immunized animals; and antibodies or libraries prepared by introducing an mutation into an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 to these antibodies and libraries (e.g., a library rich in an amino acid (e.g., histidine and glutamine acid) whose side chain has a pKa of 4.0-8.0 or rich in non-natural amino acids; and a library to which an amino acid (e.g., histidine and glutamine acid) whose side chain has a pKa of 4.0-8.0 or a non-natural amino acid mutation, is introduced into a specific site); can be used.
As a method for obtaining an antigen-binding domain or antibody having an antigen-binding activity in a low hydrogen-ion concentration condition (or high pH, i.e., a neutral pH range) higher than (the antigen-binding activity) in a high hydrogen-ion concentration condition (or low pH, i.e., acidic pH range), from a hybridoma prepared by immunization of an animal or the B cell of an immunized animal, a method as described, for example, a method described in WO2009/125825 is preferably mentioned, in which such an antigen-binding domain or antibody is obtained in accordance with this method by substituting at least one amino acid of an antigen-binding domain or an antibody with an amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) or a non-natural amino acid mutation or by inserting an amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) or a non-natural amino acid in an antigen-binding domain or an antibody.
The position, to which an amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) or a non-natural amino acid mutation is to be introduced, is not particularly limited. Any position may be accepted as long as the antigen-binding activity in an acidic pH range becomes weaker than (the antigen-binding activity) in a neutral pH range ((the value of (KD (acidic pH range)/KD (a neutral pH range) increases, or the value of kd (acidic pH range)/kd (a neutral pH range) increases) compared to before the substitution or insertion. For example, if the antigen-binding molecule is an antibody, e.g., a variable region and CDR of the antibody are preferably mentioned. The number of amino acids to be substituted with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0, or the number of amino acids to be inserted can be appropriately determined by those skilled in the art. Substitution can be made by a single amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) and a single non-natural amino acid; and insertion can be made by a single amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) and a single non-natural amino acid. Substitution can be made by a plurality of amino acids (2 or more) having a pKa of a side chain of 4.0-8.0 (for example histidine and glutamine acid) and non-natural amino acids; and insertion can be made by 2 or more amino acids having a pKa of a side chain of 4.0-8.0 (for example histidine and glutamine acid) and non-natural amino acids. In addition, other than substation or insertion of an amino acid(s) (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 (s), deletion, addition, insertion and/or substitution, etc. of other amino acid(s) can be made at the same time. The substation or insertion of an amino acid(s) (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 (s) can be made at random by a histidine scanning method, etc., which is a substantially the same method as an alanine scanning method known to those skilled in the art except that alanine is replaced by histidine, etc. From the antigen-binding domains or antibodies, to which a mutation is introduced at random by substation or insertion of an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0, an antigen-binding molecule having a larger KD (acidic pH range)/KD (a neutral pH range) or kd (acidic pH range)/kd (a neutral pH range) value, compared to before introduction of mutation, can be selected.
As a preferable example of the antigen-binding molecule, to which a mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0, is introduced, and whose antigen-binding activity in the acidic pH range is lower than the antigen-binding activity in the neutral pH range, as described above, an antigen-binding molecule whose antigen-binding activity in the neutral pH range after mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 is equivalent to the antigen-binding activity (in the neutral pH range before mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0), is preferably mentioned. In the present invention, the expression: an antigen-binding molecule after mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 has the equivalent antigen-binding activity before mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 means that the antigen-binding activity of the antigen-binding molecule after the mutation with an amino acid whose side chain has a pKa of 4.0-8.0 (for example histidine and glutamine acid) or a non-natural amino acid is at least 10% or more, preferably 50% or more, further preferably 80% or more, and more preferably 90% or more, based on the antigen-binding activity of an antigen-binding molecule before mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0, which is regarded as 100%. The antigen-binding activity after the mutation with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0 at pH 7.4 may be higher than (the antigen-binding activity) before the mutation (with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0) at pH 7.4. If the antigen-binding activity of an antigen-binding molecule is lowered by substation or insertion (with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0), the antigen-binding activity can be increased to the same level as the antigen-binding activity before substitution or insertion (with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0) by providing substitution, deletion, addition and/or insertion, etc. of a single or a plurality of amino acids to the antigen-binding molecule. The present invention includes the antigen-binding molecule, which acquires the same binding activity by substitution, deletion, addition and/or insertion, etc. of a single or a plurality of amino acids after substation or insertion with an amino acid (for example histidine and glutamine acid) or a non-natural amino acid whose side chain has a pKa of 4.0-8.0.
When an antigen-binding molecule contains an antibody constant region, as another preferable aspect of the antigen-binding molecule whose antigen-binding activity in an acidic pH range is lower than (the antigen-binding activity) in a neutral pH range, an antigen-binding molecule having a modified antibody constant region is mentioned. As a specific example of the modified antibody constant region, for example, the constant regions represented by SEQ ID NO: 9, 10, 11, or 12 are preferably mentioned.
The antigen-binding domain or antibody of the present invention to be screened by any one of the above screening methods may be prepared in any manner. For example, if the ion-concentration condition is a hydrogen ion-concentration condition or a pH condition, antibodies already exist; libraries (phage library, etc.) already exist; antibodies or libraries prepared from hybridomas (prepared by immunization of animals) or the B cells of immunized animals; and antibodies or libraries prepared by introducing an amino acid (for example histidine and glutamine acid) or a non-natural amino acid mutation whose side chain has a pKa of 4.0-8.0 to these antibodies and libraries (e.g., library rich in an amino acid and non-natural amino acid whose side chain has a pKa of 4.0-8.0 (for example, histidine and glutamine acid); and a library to which an amino acid (for example histidine and glutamine acid) or a non-natural amino acid mutation whose side chain has a pKa of 4.0-8.0 is introduced in a predetermined site); can be used. As the amino acid having such an electron donating amino acid, not only natural amino acids such as histidine or glutamine acid but also non-natural amino acids such as a histidine analog (US20090035836) or m-NO2-Tyr (pKa 7.45), 3,5-Br2-Tyr (pKa 7.21) or 3,5-I2-Tyr (pKa 7.38) (Bioorg. Med. Chem. (2003) 11 (17), 3761-2768) are preferably illustrated. In the non-natural amino acids, it is known that pKa can be artificially controlled (Angew. Chem. Int. Ed. (2005) 44, 34, Chem Soc Rev. (2004) 33 (7), 422-430, Amino Acids. (1999) 16 (3-4), 345-379).
According to a non-limiting aspect of the present invention, a library containing a plurality of antigen-binding molecules of the present invention mutually different in sequence can be prepared also by using a light-chain variable region “to which at least one amino acid residue capable of changing the binding activity of an antigen-binding molecule to an antigen depending upon the hydrogen ion-concentration condition” is introduced, in combination with a heavy-chain variable region, which is prepared as a randomized variable region sequence library.
As a non-limiting example of the amino acid residue, an amino acid residue contained in CDR1 of a light chain is illustrated. Other than this, as a non-limiting example of the amino acid residue, an amino acid residue contained in CDR2 of a light chain is illustrated. In another non-limiting example of the amino acid residue, an amino acid residue contained in CDR3 of a light chain is also illustrated.
As a non-limiting example of the amino acid residue contained in CDR1 of a light chain as described above, the amino acid residues in CDR1 of a light-chain variable region at the position 24, position 27, position 28, position 31, position 32, and/or position 34 (represented by Kabat numbering) are mentioned. Furthermore, as a non-limiting example of the amino acid residue contained in CDR2 of a light chain, the amino acid residues in CDR2 of a light-chain variable region at the position 50, position 51, position 52, position 53, position 54, position 55, and/or position 56 (represented by Kabat numbering) are mentioned. As a non-limiting example of the amino acid residue contained in CDR3 of a light chain, the amino acid residues in CDR3 of a light-chain variable region at the position 89, position 90, position 91, position 92, position 93, position 94, and/or position 95A (represented by Kabat numbering) are mentioned. As long as these amino acid residues change the binding activity of an antigen-binding molecule to an antigen depending upon the hydrogen ion-concentration condition, these amino acid residues can be contained singly or in combination of two or more.
In the present invention, as non-limiting examples of the site to be substituted with histidine or a non-natural amino acid, for example, the following sites described in WO2009/125825 are mentioned. Note that, the amino acid positions are specified in accordance with the Kabat numbering.
Heavy chain: H27, H31, H32, H33, H35, H50, H58, H59, H61, H62, H63, H64, H65, H99, H100b, H102
Light chain: L24, L27, L28, L32, L53, L54, L56, L90, L92, L94
Of these modification sites, H32, H61, L53, L90 and L94 are considered as highly universal modification sites; however, the modification sites are not limited to these and can be appropriately designed depending upon the purpose.
Although it is not particularly limited, as preferable modification sites when the antigen is an IL-6 receptor (for example, human IL-6 receptor), the following sites can be mentioned.
Heavy chain: H27, H31, H32, H35, H50, H58, H61, H62, H63, H64, H65, H100b, H102
Light chain: L24, L27, L28, L32, L53, L56, L90, L92, L94
When a plurality of sites in combination are substituted by histidine or a non-natural amino acid, specific examples of preferable combinations can include a combination of H27, H31 and H35, a combination of H27, H31, H32, H35, H58, H62 and H102, a combination of L32 and L53, and a combination of L28, L32 and L53. Furthermore, as an example of a preferable combination of substation sites in a heavy chain and a light chain, a combination of H27, H31, L32 and L53 can be mentioned. One and a plurality of sites of these sites can be substituted with histidine or non-natural amino acid.
When an antigen-binding molecule contains an antibody constant region, as another method for changing the binding of an antigen-binding molecule to an antigen depending upon the ion-concentration condition, a method for modifying an amino acid in an antibody constant region can be also mentioned. Specific examples of such an antibody constant region can include antibody constant regions (SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16) having a substitution(s), which is inserted by the method as described in Examples WO2009/125825. As a method for modifying an antibody constant region, for example, a method of investigating a plurality of isotypes (IgG1, IgG2, IgG3, IgG4) of a constant region and selecting an isotype reducing the antigen-binding activity in an acidic pH range (a dissociation rate in the acidic pH range increases) is mentioned. Another method of reducing the antigen-binding activity in an acidic pH range (a dissociation rate in the acidic pH range increases) by introducing an amino acid substitution in a wild type isotype amino acid sequence (wild type IgG1, IgG2, IgG3, IgG4 amino acid sequence) is mentioned. The sequence of the hinge region of an antibody constant region greatly varies between isotypes (IgG1, IgG2, IgG3, IgG4). Since the difference in amino acid sequence of the hinge region has a large effect upon antigen-binding activity, if an isotype is appropriately selected in consideration of the types of antigen and epitope, the antigen-binding activity in an ion-concentration condition, for example, the acidic pH range, can be decreased (dissociation rate in the acidic pH range increases). Furthermore, since the difference in amino acid sequence of the hinge region has a large effect upon antigen-binding activity, as the amino acid substitution site in the amino acid sequence of a wild type isotype, a hinge region is presumably desirable.
An antigen-binding molecule whose binding activity to an antigen changes depending upon the ion-concentration condition, can be prepared by introducing a substitution or insertion of an amino acid(s) in an antigen-binding molecule not having a such a property by use of a method as mentioned above. Another method, a method for directly obtaining an antigen-binding molecule having such a property is mentioned. For example, an antibody having a desired property can be directly obtained by immunizing, an animal (mouse, rat, hamster, rabbit, transgenic mouse with a human immunoglobulin, transgenic rat with a human immunoglobulin, transgenic rabbit with a human immunoglobulin, lama, camel, etc.) with an antigen to obtain antibodies and screening the antibodies based on the binding to the antigen in an ion concentration depending manner. Furthermore, an antibody having a desired property can be directly obtained from an antibody library prepared in-vitro by screening based on the binding to the antigen performed in an ion concentration depending manner. Such a method is not particularly limited.
For modification of amino acid(s) of an antigen-binding domain, a method known in the art such as a site-directed mutation inducing method (Kunkel, et al. (Proc. Natl. Acad. Sci. USA (1985) 82, 488-492)) and an Overlap extension PCR can be appropriately employed. As a modification method for substituting with an amino acid(s) except natural amino acid(s), a plurality of known methods can be employed (Annu. Rev. Biophys. Biomol. Struct. (2006) 35, 225-249, Proc. Natl. Acad. Sci. U.S.A. (2003) 100 (11), 6353-6357). For example, an acellular translation system (Clover Direct (Protein Express)) containing tRNA having a non-natural amino acid bound to a complementary amber suppressor tRNA of a termination codon, i.e., UAG codon (amber codon) is preferably used.
In a non-limiting aspect of the present invention, a pharmaceutical composition, which contains an antigen-binding molecule containing an FcRn binding domain, an antigen-binding domain whose binding activity to an antigen changes depending upon the ion-concentration condition, and one or more sugar chain receptor-binding domains whose binding activity to a sugar chain receptor changes depending upon the ion-concentration condition, is provided. Generally, the neutralization activity refers to an activity that inhibits the biological activity of a ligand such as a virus and a toxin having a biological activity against cells. More specifically, a substance having a neutralization activity refers to a substance which binds to a ligand or a receptor to which the ligand binds to thereby inhibit binding between the ligand and the receptor. The receptor whose binding with the ligand is inhibited by the neutralization activity cannot exhibit a biological activity via the receptor. If the antigen-binding molecule is an antibody, an antibody having such a neutralization activity is generally called as a neutralizing antibody. The neutralization activity of a test substance is determined by comparing the biological activity in the presence of a ligand and in the presence or absence of the test substance.
For example, as a major ligand for IL-6R, IL-6 represented by SEQ ID NO: 17 is conceivably and preferably mentioned. IL-6R is a type I membrane protein (in which the amino terminal thereof forms an extracellular domain) forms a hetero tetramer together with a gp130 receptor (which is induced to form a dimer by IL-6) (HEINRICH, et al. (Biochem. J. (1998) 334, 297-314)). When the hetero tetramer is formed, Jak associated with the gp130 receptor is activated. Jak phosphorylates itself and a receptor. The phosphorylated sites of the receptor and Jak each serve as a binding site to a molecule belonging to a Stat family having SH2 such as Stat 3, MAP kinase and PI3/Akt, and other proteins and adaptors having SH2. Subsequently, Stat that binds to a gp130 receptor is phosphorylated by Jak. The phosphorylated Stat forms a dimer and migrates into a nucleus to control transcription of a target gene. Jak or Stat can be involved in a signal cascade via a receptor of another class. The signal cascade of IL-6 out of control is observed in the pathological condition of an autoimmune disease, inflammation, multiple myeloma and cancer such as prostatic cancer. Stat3, which may serve as a cancer gene, is constantly activated in many cancers. In prostatic cancer and multiple myeloma, there is a crosstalk between the signal cascade of IL-6R and the signal cascade of an epithelial growth factor receptor (EGFR) family member (Ishikawa, et al. (J. Clin. Exp. Hematopathol. (2006) 46 (2), 55-66)).
Since such a signal cascade within a cell varies depending upon the type of cell, a target molecule can be appropriately set every desired target cell and is not limited to the forementioned factors. Neutralization activity can be evaluated by measuring activation of an in-vivo signal. Also, the activation of the in-vivo signal can be detected based on transcription inducing effect on a target gene present downstream of the in-vivo signal cascade. A change of transcription activity of a target gene can be detected based on the principle of reporter assay. Specifically, a reporter gene, such as GFP (Green Fluorescence Protein) or luciferase, is arranged downstream of a transcription factor or a promoter region of a target gene and the reporter activity is measured. In this manner, a change of transcription activity can be measured as reporter activity. As a measurement kit for in-vivo signal activation, a commercially available kit can be appropriately used (for example, Mercury Pathway Profiling Luciferase System (Clontech), etc.).
The neutralization activity of a ligand for a receptor (such as EGF receptor family) working on a signal cascade (generally activating cell growth) is measured by determining growth activity of a target cell. In this manner, the neutralization activity of the neutralizing antibody can be evaluated. For example, the suppression effect against growth of cells, which is promoted by a growth factor of an EGF family such as HB-EGF, can be evaluated or determined based on the neutralization activity of an anti HB-EGF antibody preferably in accordance with the following method. The cell growth suppression activity can be evaluated or determined in-vitro by measuring uptake of thymidine labeled with [3H] and added to a medium by living cells, as an index for determining a DNA replication ability. As a further simple method, a dye-exclusion test and an MTT method are used. The former one is a method of measuring the ability of a cell to exclude a dye such as trypan blue out of the cell under a microscope. The latter one is a method using an ability of a living cell to convert a tetrazolium salt, i.e., MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) into formazan emitting blue color. To describe it more specifically, a test antibody is added together with a ligand to a culture fluid of a test cell. After the passage of a predetermine time, an MTT solution is added to the culture fluid and allowed to stand still for a predetermined time to allow the cells to take MTT. As a result, MTT (yellow compound) is converted into a blue compound by succinic acid dehydrogenase present within mitochondria in the cell. After the blue product is dissolved to allow the product to emit color, its absorbance is measured and used as an index of the number of living cells. Other than MTT, reagents such as MTS, XTT, WST-1 and WST-8 are commercially available (Nacalai Tesque, etc.) and can be preferably used. In measuring the activity, a binding antibody, which is an antibody having the same isotype as the anti HB-EGF antibody and having no cell growth suppression activity is used as a control antibody similarly to an anti HB-EGF antibody. Activity can be determined if the anti HB-EGF antibody shows a stronger cell growth suppression activity than the control antibody.
As the cells for use in evaluation of the activity, for example, a cell whose growth is promoted by HB-EGF, i.e., ovary cancer cell namely, RMG-1 cell strain, and a mouse Ba/F3 cell, which is transformed with a vector, in which a gene encoding a fusion protein hEGFR/mG-CSFR (human EGFR extracellular domain and a mouse GCSF receptor intracellular domain are fused in frame) is connected so as to express the gene, can be preferably used. As described above, those skilled in the art can appropriately select a cell for use in evaluating the activity and use the cell in measurement of the cell growth activity.
It is not necessary for the antigen-binding molecule provided by the present invention to have a neutralization activity by itself since the antigen-binding molecule can clear an antigen out of plasma. However, it is further preferable that the antigen-binding molecule exhibits the neutralization activity to an antigen to block the action of an antigen present in the plasma until the antigen is taken up into the cell expressing an Fcγ receptor together with the antigen-binding molecule by endocytosis via the Fcγ receptor.
Since the antigen-binding molecule (provided by the present invention) can promote dissociation of an antigen (which binds to the antigen-binding molecule outside the cell) from the antigen-binding molecule within the cell, the antigen dissociated from the antigen-binding molecule within the cell is decomposed in a lysosome. Therefore, it is not always necessary for the antigen-binding molecule itself to have a neutralization activity. However, it is further preferable that the antigen-binding molecule preferably exhibits the neutralization activity to an antigen to block the action of an antigen present in the plasma until the antigen is taken up into the cell expressing a sugar chain receptor, together with the antigen-binding molecule by endocytosis via the sugar chain receptor.
Since the antigen-binding molecule (provided by the present invention) can reduce the total antigen concentration or free antigen concentration in plasma, it is not always necessary for the antigen-binding molecule itself to have a neutralization activity. However, it is further preferable that the antigen-binding molecule exhibits the neutralization activity to an antigen to block the action of an antigen present in the plasma until the antigen is taken up into the cell expressing a sugar chain receptor together with the antigen-binding molecule by endocytosis via the sugar chain receptor.
The sugar chain refers to a group of compounds in which various types of sugar molecules are connected via a glycoside linkage. Most of sugar chains are present in-vivo as a complex molecule in which a sugar molecule binds to a protein or a lipid, which is generally called a glycoconjugate. Of them, a glycoconjugate, which is a sugar bound to a protein, is a glycoprotein.
As an example of the sugar chain (to be used in the present invention), which is recognized by a sugar chain receptor, more specifically, to which a sugar chain receptor-binding domain binds, a sugar chain constituting a glycoprotein is mentioned. Examples of the sugar chain of a glycoprotein include an O-linked sugar chain and an N-linked sugar chain are mentioned. More preferable example of the sugar chain of a glycoprotein, an N-linked sugar chain is mentioned.
The O-linked sugar chain of a glycoprotein is obtained by connecting a sugar chain to the hydroxy group of a serine or threonine residue of a protein via an O-glycoside linkage. The sugar directly binding to a serine or threonine residue is mostly N-acetylgalactosamine (GalNAc). The core structure thereof consists of 8 elements: (1) galactose (Gal) connected to N-acetylgalactosamine (GalNAc) via a β1-3 linkage, (2) Gal connected to GalNAc via a β1-3 linkage and N-acetylglucosamine (GlcNAc) connected to GalNAc via a β1-6 linkage, (3) GlcNAc connected to GalNAc via a β1-3 linkage, (4) GlcNAc connected to GalNAc via a β1-3 linkage and GlcNAc connected to GalNAc via a β1-6 linkage, (5) GlcNAc connected to GalNAc via a β1-6 linkage, (6) GalNAc connected to GalNAc via a β1-6 linkage, (7) Gal connected to GalNAc via a β1-3 linkage.
N-linked sugar chains of glycoproteins all have a common core unit structure, Man 6 (Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc. This is called a tri-mannosyl core. N-linked sugar chains are divided into three sub-groups based on the structure and the site of the sugar residue(s) added to the tri-mannosyl core.
Of them, a complex type sugar chain does not contain a mannose residue except a tri-mannosyl core. At the reducing end of a side chain, a GlcNAc residue is present and connected to two α-mannosyl residues of the tri-mannosyl core.
A high-mannose sugar chain contains only α-mannose residues in addition to a tri-mannosyl core. In the sugar chain of this group, seven sugars are contained as core units, like Manα1-6 (Manα1-3)Manα1-6 (Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc.
In the complex sugar chain, one or two α-mannosyl groups are connected to a Manα1-6 arm of a tri-mannosyl core, in the same manner as in a high mannose, and the same side chain as that of the complex sugar chain is connected to the Manα1-3 arm of the core. The presence or absence of a fucose linkage to the position C-6 of GlcNAc, which is positioned at the reducing end of the tri-mannosyl core and furthermore, the presence or absence of β-GlcNAc linkage (called bisecting GlcNAc) to the position C-4 of a β mannosyl residue contribute to diversity of the structure of a complex sugar chain. Of the three N-linked sugar chain sub groups, a complex type contains the most diversified structures.
The sugar chain receptor refers to a receptor recognizing the aforementioned sugar chain and binding it. As long as it recognizes and binds to the sugar chain, any molecule can be used as a sugar chain receptor. A preferable receptor is a receptor expressed on a cell. For example, it is disclosed that an O-linked sugar chain on CD99 plays an important role in binding with PILR (paired Ig-like type-II receptor) (The Journal of immunology (2008) vol. 180 (3), 1686-1693). Furthermore, it is known that an asialoglycoprotein receptor binds to an N-linked sugar chain having galactose at a terminal thereof. Moreover, it is known that a mannose receptor binds to an N-linked sugar chain having mannose at a terminal thereof. These receptors are preferably used as a sugar chain receptor in the present invention. More specifically, in the present invention, the antigen-binding molecule has a domain (sugar chain receptor-binding domain) binding to such a receptor. Thus, if the sugar chain receptor is an asialoglycoprotein receptor, an N-linked sugar chain having galactose at a terminal thereof can be preferably used as a sugar chain receptor-binding domain contained in the antigen-binding molecule of the present invention. Furthermore, if the sugar chain receptor is a mannose receptor, an N-linked sugar chain having mannose at a terminal thereof can be preferably used as a sugar chain receptor-binding domain contained in the antigen-binding molecule of the present invention
The antigen-binding molecule of the present invention has one or more binding domain to a sugar chain receptor (particularly a human sugar chain receptor). The binding domain to a sugar chain receptor (particularly, a human sugar chain receptor) is not particularly limited in type and number, as long as the antigen-binding molecule has a binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range and as long as the binding activity to the sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range. Furthermore, a domain having a binding activity directly or indirectly to a sugar chain receptor (particularly, a human sugar chain receptor) can be used. Examples of such a domain may include a sugar chain having an activity directly binding to a sugar chain receptor (particularly, a human sugar chain receptor); an Fc domain of an IgG immunoglobulin; an antibody against a sugar chain receptor (particularly, a human sugar chain receptor); a peptide that binds to a sugar chain receptor (particularly, a human sugar chain receptor); and a Scaffold molecule to a sugar chain receptor (particularly, a human sugar chain receptor). In the present invention, a sugar chain receptor-binding domain, which has a binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range and whose binding activity to the sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range, is preferred. The domain can be used as it is as long as the domain already has the binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range and as long as the binding activity to a sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range. The binding activity between a sugar chain receptor-binding domain, which has an N-linked sugar chain having galactose at a terminal thereof, and an asialoglycoprotein receptor (a sugar chain receptor binding to the sugar chain) in an acidic pH range is preferably mentioned as an example where the binding activity is lower than the binding activity in the neutral pH range. Also, the binding activity between a sugar chain receptor-binding domain, which has an N-linked sugar chain having mannose at a terminal thereof, and a mannose receptor (a sugar chain receptor binding to the sugar chain) in an acidic pH range is preferably mentioned as an example where the binding activity is lower than the binding activity in the neutral pH range.
In the case where the binding activity of a sugar chain receptor-binding domain to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range is zero or weak, the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) can be acquired by modifying an amino acid in the antigen-binding molecule. Alternatively, the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor), can be enhanced by modifying an amino acid in the domain already having the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range. With respect to modification of an amino acid in the binding domain to a sugar chain receptor (particularly, a human sugar chain receptor), a desirable modification can be found out by comparing the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the neutral pH range between before and after modification of the amino acid.
In the case where the binding activity of a sugar chain receptor-binding domain to a sugar chain receptor (particularly, a human sugar chain receptor) in an acidic pH range is not lower than (the binding activity to a sugar chain receptor (particularly, a human sugar chain receptor)) in a neutral pH range, the binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in the acidic pH range lower than the binding activity (to a sugar chain receptor (particularly, a human sugar chain receptor)) in a neutral pH range can be acquired by modifying an amino acid in the antigen-binding molecule. With respect to modification of an amino acid in the binding domain to a sugar chain receptor (particularly, a human sugar chain receptor), a desirable modification can be found out by comparing the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the acidic pH range to the binding activity (to a sugar chain receptor (particularly, a human sugar chain receptor)) in the neutral pH range between before and after modification of an amino acid.
In the present invention, a sugar chain receptor-binding domain can be introduced into a site other than the antigen-binding domain and an FcRn binding domain constituting an antigen-binding molecule. Furthermore, as long as binding to an antigen by an antigen-binding domain is not inhibited, a sugar chain receptor-binding domain can be introduced in any site of the structure of the antigen-binding molecule. The site can be introduced into the antigen-binding domain as long as binding to an antigen by the antigen-binding domain is not inhibited and can be introduced into a site other than the antigen-binding domain. Furthermore, in another aspect, as long as a sugar chain receptor-binding domain does not inhibit the binding between the FcRn binding domain of an antigen-binding molecule and FcRn (particularly human FcRn), the sugar chain receptor-binding domain can be introduced into any site of the structure of the antigen-binding molecule. For example, the hinge portion of an IgA antibody can be a candidate for an amino acid sequence of the sugar chain receptor-binding domain for binding an O-linked sugar chain. A motif sequence, to which an N-linked sugar chain (i.e., Asn-X-Ser/Thr where X is amino acid except Pro) is added, can be a candidate for amino acid sequence of the sugar chain receptor-binding domain for binding the N-linked sugar chain. A gene encoding an antigen-binding molecule containing such an amino acid sequence is introduced into a host cell (described later) and cultured. From the culture fluid, the antigen-binding molecule of the present invention containing a sugar chain receptor-binding domain, to which a desired sugar chain is bound, can be produced.
In the present invention, a sugar chain receptor-binding domain may be chemically produced. For example, a chemical ligand such as a galactose derivative, which imitates an N-linked sugar chain having a galactose terminal; a mannose derivative, which imitates a high-mannose sugar chain; and a derivative which imitates sialic acid, may covalently conjugate to an antigen-binding molecule. Examples of such a chemical ligand include the molecules described in Bioorg. Med. Chem. (2011) 19 (8), 2494-2500, Bioorg. Med. Chem. (2009) 17 (20), 7254-7264, Bioorg. Med. Chem. (2008) 16 (9), 5216-5231, J. Am. Chem. Soc. (2004) 126 (33), 10355-10363, J. Pept. Sci. (2003) 9 (6), 375-385, Methods Enzymol. (2010) 478, 343-363, but not limited to these. Examples of the amino acid at the antigen binding site, to which a chemical ligand is be conjugated, include lysine and cysteine, but not limited to these. A method for conjugating a chemical ligand to a specific site of an antigen-binding molecule, a method known to those skilled in the art can be employed, such as a method of substituting the amino acid at a conjugation site with cysteine, or a method of substituting lysine at a site where no conjugate is desired, with another amino acid. As a conjugation method, a known method to those skilled in the art can be used, such as a method of reacting maleimide and thiol of cysteine and a method of reacting an activated ester and lysine.
Conditions other than pH in measuring the binding activity to an antigen and FcRn (particularly human FcRn) can be appropriately selected by those skilled in the art and a method for measuring the binding activity is not limited to a specific method. For example, the binding activity can be measured in MES buffer at 37° C., as described in WO2009/125825. Furthermore, the antigen-binding activity of an antigen-binding molecule and the binding activity to, FcRn (particularly human FcRn) can be measured by a known method to those skilled in the art, such as Biacore (GE Healthcare). When the antigen is a soluble antigen, the binding activity of an antigen-binding molecule to an antigen is measured and evaluated by feeding the antigen as an analyte to a chip having the antigen immobilized thereto. If the antigen is a membrane antigen, the binding activity to the membrane antigen can be evaluated by feeding an antigen-binding molecule as an analyte to a chip having the antigen immobilized thereto. The binding activity of an antigen-binding molecule to FcRn (particularly human FcRn) is measured and evaluated by feeding FcRn (particularly human FcRn) or the antigen-binding molecule as an analyte to a chip having the antigen-binding molecule or FcRn (particularly human FcRn) immobilized thereto.
In the present invention, the binding activity to FcRn (particularly human FcRn) in an acidic pH range refers to the binding activity to FcRn (particularly human FcRn) at pH 4.0 to pH 6.5. The binding activity to FcRn (particularly human FcRn) in an acidic pH range refers to the binding activity to an antigen preferably at an arbitrary pH from pH 5.5 to pH 6.5, for example, the antigen-binding activity to an antigen at pH selected from pH 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, and 6.5, particularly preferably, at an arbitrary pH from pH 5.8 to pH 6.0 close to the pH in early-stage endosome in-vivo, for example, pH selected from pH 5.80, 5.81, 5.82, 5.83, 5.84, 5.85, 5.86, 5.87, 5.88, 5.89, 5.90, 5.91, 5.92, 5.93, 5.94, 5.95, 5.96, 5.97, 5.98, 5.99, and 6.00.
At any temperature from 10° C. to 50° C. as the temperature for measuring the binding activity, the binding activity of the antigen-binding molecule (of the present invention) containing an FcRn binding domain to FcRn (particularly human FcRn) can be evaluated. Preferably, the binding activity of the antigen-binding molecule (of the present invention) containing an FcRn binding domain to FcRn (particularly human FcRn) can be measured at any temperature from 15° C. to 40° C. More preferably, the binding activity of the antigen-binding molecule (of the present invention) containing an FcRn binding domain to FcRn (particularly human FcRn) can be measured at any temperature from 20° C. to 35° C., for example, selected from 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, and 35° C.
In the present invention, the expression: “the binding to an antigen is not inhibited by an antigen-binding domain” means that the antigen-binding activity of an antigen-binding molecule after introduction of an sugar-chain receptor binding domain is maintained at a level of 20% or more, preferably 50% or more, further preferably 80% or more, more preferably 90% or more of the antigen-binding activity of the antigen-binding molecule before the introduction of the sugar chain receptor-binding domain. When the antigen-binding activity of an antigen-binding molecule decreases by the introduction of the sugar chain receptor-binding domain, the antigen-binding activity can be changed to the same level as the antigen-binding activity before the sugar chain receptor-binding domain is introduced, by substitution, deletion, addition and/or insertion of one or a plurality of amino acids in the antigen-binding molecule. The present invention also includes the antigen-binding molecule that regains the binding activity to the same level as that before the introduction by such a substitution, deletion, addition and/or insertion of one or a plurality of amino acids performed after the introduction of a sugar chain receptor-binding domain. Furthermore, the expression: “the binding to FcRn (particularly human FcRn) is not inhibited by a sugar chain receptor-binding domain” means that the binding activity of an antigen-binding molecule to FcRn (particularly human FcRn) after introduction of an sugar-chain receptor binding domain is maintained at a level of 20% or more, preferably 50% or more, further preferably 80% or more, more preferably 90% or more of the binding activity of the antigen-binding molecule to FcRn (particularly human FcRn) before the introduction of the sugar chain receptor-binding domain. When the binding activity of an antigen-binding molecule to FcRn (particularly human FcRn) decreases by the introduction of a sugar chain receptor-binding domain, the binding activity can be changed to the same level as the binding activity to FcRn (particularly human FcRn) before the sugar chain receptor-binding domain is introduced, by substitution, deletion, addition and/or insertion of one or a plurality of amino acids in the antigen-binding molecule. The present invention also include the antigen-binding molecule that regains the binding activity to the same level as that before the introduction, even if such a substitution, deletion, addition and/or insertion of one or a plurality of amino acids is performed after the introduction of a sugar chain receptor-binding domain. A measurement method and determination method of the binding activity to an antigen or FcRn (particularly human FcRn) will be described later.
As an example of the sugar chain receptor-binding domain contained in the antigen-binding molecule in the present invention, a sugar chain receptor-binding domain having a desired sugar chain bound thereto is preferably mentioned. As an example of the desired sugar chain, an O-linked sugar chain or an N-linked sugar chain is preferably mentioned. As a method of binding a sugar chain to a sugar chain receptor-binding domain, a method known in the art can be employed. For example, an enzymatic method performed in an acellular system as described in (Japanese Patent Laid-Open No. 2006-141241), which is a method for producing an antibody modified after translation in an acellular protein synthesis system, comprising preparing a cell extract from cultured cells of an immortalized mammalian animal cell strain capable of secreting a protein and adding mRNA encoding an antibody to the extract, can be employed as a method for producing the sugar chain receptor-binding domain having a desired sugar chain bound thereto. Furthermore, in one of such methods known in the art, a gene, to which a motif sequence for adding a desired sugar chain is introduced by a genetic recombination technique, etc., and which encodes a sugar chain receptor-binding domain contained in an antigen-binding molecule present in nature or artificially produced is introduced into a host cell, which is then cultured. From the culture fluid of the host cell, the antigen-binding molecule of the present invention containing a sugar chain receptor-binding domain, to which a desired sugar chain to be bound, can be produced.
When the sugar chain is an O-linked sugar chain, a motif sequence, to which the O-linked sugar chain is added, can be designed by use of database known in the art. An O-linked sugar chain is added to the hinge portion of an IgA antibody. A gene sequence encoding such a sugar chain receptor-binding domain having an O-linked sugar chain added thereto, already known in the art, will be used as a candidate for the motif sequence. When the sugar chain is an N-linked sugar chain, a motif sequence, to which the N-linked sugar chain is added, is known to be a motif consisting of three continuous amino acids: Asn-X-Ser/Thr. Because of this, if a gene, which encodes an antigen-binding molecule containing a sugar chain receptor-binding domain and which is designed so as to encode the motif sequence consisting of Asn-X-Ser/Thr for adding an N-linked sugar chain by a genetic recombination technique, etc. is introduced into a host cell (described later) and cultured, the antigen-binding molecule of the present invention containing the sugar chain receptor-binding domain, to which a desired sugar chain is to be bound, can be produced, from the culture fluid of the host cell.
The antigen-binding molecules produced as mentioned above may have the same sugar chain structure in some cases; whereas, the antigen-binding molecules are produced as a mixture of the antigen-binding molecules having different sugar chains added thereto in other cases. In the present invention, such a mixture can be also preferably used. Also, an antigen-binding molecule having a sugar-chain binding domain to which a specific sugar chain is connected, can be preferably used in the present invention.
As a method for connecting a specific sugar chain to the sugar chain receptor-binding domain contained in the antigen-binding molecule (of the present invention), a plurality of methods known in the art can be employed. As one of the known methods, a method of purifying an antigen-binding molecule having a specific sugar chain by use of a property of a sugar chain of a natural antigen-binding molecule or an artificial antigen-binding molecule (prepared by a genetic recombination method, etc.) is mentioned. An antibody having high-mannose sugar chain is known to be purified by affinity chromatography using ConA-sepharose (Millward (Biologicals (2008) 36, 49-60)). Such a purification method can be used for preparing an antigen-binding molecule having an N-linked sugar chain having mannose at the non-reducing end, in the present invention.
Furthermore, in another aspect, in order to obtain an antigen-binding molecule having a specific sugar chain, an enzyme treatment can be appropriately employed. As described later in Examples, an antigen-binding molecule having an N-linked sugar chain having galactose at the non-reducing end can be prepared from an antigen-binding molecule having a complex sugar chain having sialic acid at the non-reducing end, by a sialidase treatment. Furthermore, an antibody having a high-mannose sugar chain is known to be prepared by sialidase and β galactosidase treatment, by which galactose is removed from the sugar chain (Newkirk (Clin. Exp. Immunol. (1996) 106, 259-264)). Such a preparation method including treatments with sialidase and β galactosidase can be used for preparing an antigen-binding molecule having an N-linked sugar chain having mannose at a non-reducing end, in the present invention.
In another aspect, in order to obtain the antigen-binding molecule having a specific sugar chain of the present invention, a method of recovering the antigen-binding molecule from a culture fluid of a host cell, which is transfected with a recombinant gene encoding the antigen-binding molecule and whose glycosidase activity is modified so as to accumulate a specific sugar chain (by a method including genetic or genetic recombination technique but not limited to these), can be appropriately employed. It is known that an antibody having a high mannose N-linked sugar chain is collected from a culture fluid of a Lec1 mutation strain, which is derived from a CHO cell defective in N-acetylglucosaminyltransferase I activity and transfected with a recombinant gene encoding the antibody (Wright and Morrison (J. Exp. Med. (1994) 180, 1087-1096)). In the present invention, an antigen-binding molecule having an N-linked sugar chain having mannose at the non-reducing end can be collected from a culture fluid of a Lec1 mutation strain transfected with a recombinant gene encoding the antigen-binding molecule.
In another aspect, in order to obtain the antigen-binding molecule having a specific sugar chain of the present invention, a method for collecting an antigen-binding molecule having a specific sugar chain and accumulated in a culture fluid by culturing a cell producing the antigen-binding molecule with the addition of an inhibitor for inhibiting a specific glycosidase reaction, can be appropriately employed. It is known that an antibody having a high mannose N-linked sugar chain having no fucose at its reducing end is collected from a culture fluid of a CHO cell producing the antibody and cultured with the addition of kifunesine (Zhou (Biotechnol. Bioeng. (2008) 99, 652-665)). In the present invention, an antibody having an N-linked sugar chain having no fucose at its reducing end and having mannose at the non-reducing end, can be collected from a culture fluid of a CHO cell transfected with a recombinant gene encoding the molecule and cultured with the addition of kifunesine. Furthermore, the antigen-binding molecule having a specific sugar chain of the present invention can be obtained by culturing a host cell whose glycosidase activity is changed as mentioned above, with the addition of an inhibitor mentioned above. Since it is known that an antibody having a specific sugar chain can be collected by such a combination (Kanda, et al. (Glycobiology (2007) 17, 104-118)), the same combination can be appropriately employed in order to obtain an antigen-binding molecule having a specific sugar chain, in the present invention
A method of expressing a protein having a specific sugar chain structure by genetically modifying a host such as Pichia pastor is known (Biochemistry. 2008 Sep. 30; 47 (39): 10294-304., J Biotechnol. 2009 Feb. 23; 139 (4): 318-25., Nat Biotechnol. 2006 February; 24 (2): 210-5.). By use of such a method, an antigen-binding molecule having a specific sugar chain structure (for example, N-linked sugar chain having a galactose terminal) uniformly bound to an N-linked glycosylation sequence can be prepared.
An antigen-binding molecule containing a sugar chain receptor-binding domain (particularly an antigen-binding molecule containing a human derived sugar chain receptor binding domain) according to the present invention binds to a sugar chain receptor in a pH-dependent manner and/or having a sugar chain receptor binding activity (particularly a human-derived sugar chain receptor binding activity) in a neutral pH range. If the binding activity to a sugar chain receptor in an acidic pH range can be lowered than (the binding activity to the sugar chain receptor) in a neutral pH range, the uptake of an antigen into a cell by the antigen-binding molecule can be promoted. If such an antigen-binding molecule is injected, the antigen concentration in plasma can be reduced more and more and the pharmacokinetics of the antigen-binding molecule can be improved, with the result that the number of antigens that can be bound by a single antigen-binding molecule can be increased.
In the present invention, the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in an acidic pH range refers to the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in the range pH 4.0 to pH 6.5, preferably at arbitrary pH in the range of pH 5.5 to pH 6.5, for example, at a pH value selected from pH 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, and 6.5, and particularly preferably, at arbitrary pH from pH 5.8 to pH 6.0 close to pH in early-stage endosome in-vivo, for example, pH selected from pH 5.80, 5.81, 5.82, 5.83, 5.84, 5.85, 5.86, 5.87, 5.88, 5.89, 5.90, 5.91, 5.92, 5.93, 5.94, 5.95, 5.96, 5.97, 5.98, 5.99, and 6.00. Furthermore, in the present invention, the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in a neutral pH range refers to the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in the range pH 6.7 to pH 10.0, at arbitrary pH in the range of pH 7.0 to pH 8.0, for example, at a pH value selected from pH 7.0, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, and 8.0, and particularly preferably, at pH 7.4 close to pH in plasma in-vivo.
Conditions other than pH in measuring the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) can be appropriately selected by those skilled in the art and are not particularly limited to specific conditions. The binding activity can be measured in MES buffer at 37° C. as described, for example, in WO2009/125825. The binding activity of an antigen-binding molecule to a sugar chain receptor (particularly a human-derived sugar chain receptor) can be measured by a method known to those skilled in the art, for example, by use of Biacore (GE Healthcare), etc. The binding activity of an antigen-binding molecule to a sugar chain receptor (particularly a human-derived sugar chain receptor) can be measured and evaluated by feeding the antigen-binding molecule as an analyte to a chip having a sugar chain receptor (particularly a human-derived sugar chain receptor) immobilized thereto. Conversely, the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) can be evaluated by feeding a solubilized sugar chain receptor (particularly a human-derived sugar chain receptor) as an analyte to a chip having the antigen-binding molecule immobilized thereto.
In the present invention, as long as the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) in an acidic pH range is weaker than (the antigen-binding activity) in a neutral pH range, the ratio of the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in the acidic pH range relative to the binding activity to the sugar chain receptor (particularly a human-derived sugar chain receptor) in the neutral pH range is not particularly limited. A KD (pH 5.8)/KD (pH 7.4) value, which is a ratio of KD (Dissociation constant) to a sugar chain receptor (particularly a human-derived sugar chain receptor) at pH 5.8 relative to KD at pH 7.4 is 2 or more, more preferably 10 or more and further preferably 40 or more. The upper limit of the KD (pH 5.8)/KD (pH 7.4) value is not particularly limited. As long as preparation can be made by those skilled in the art, any value such as 400, 1000 and 10000 may be used.
As a value representing the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor), KD (dissociation constant) is used. KD (dissociation constant) can be determined by a method known to those skilled in the art. For example, Biacore (GE healthcare), Scatchard plot, a flow cytometer, etc. are preferably used.
In the present invention, as another index representing the ratio of the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) in an acidic pH range relative to the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) in a neutral pH range, for example, a dissociation rate constant, kd (Dissociation rate constant) can be preferably used. When kd (dissociation rate constant) is used in place of KD (dissociation constant) as the index representing the ratio of the binding activities, a value of kd (in the acidic pH range)/kd (in the neutral pH range), which is a ratio of kd (dissociation rate constant) of a sugar chain receptor (particularly a human-derived sugar chain receptor) in the acidic pH range relative to kd (dissociation rate constant) in the neutral pH range, is preferably 2 or more, more preferably 5 or more, further preferably 10 or more and further more preferably 30 or more. The upper limit value of kd (in the acidic pH range)/kd (in the neutral pH range) is not particularly limited. As long as preparation can be made by common technical knowledge of those skilled in the art, any value such as 50, 100 and 200 may be used.
An asialoglycoprotein receptor (a sugar chain receptor) interacts with galactose in a pH-dependent manner and is known to exhibit a high binding activity in a neutral pH range but a low binding activity in an acidic pH range (J Biol Chem Vol. 274, No. 50, pp. 35400-35406, 1999). Similarly, a mannose receptor (a sugar chain receptor) interacts with galactose in a pH-dependent manner and is known to exhibit a high binding activity in a neutral pH range but low binding activity in an acidic pH range (J Biol Chem. 1994 Nov. 11; 269 (45): 28405-13.). From this, in the present invention, as a sugar chain/sugar chain receptor, galactose/asialoglycoprotein receptor and mannose/mannose receptor can be preferably used.
The binding activity of the galactose/asialoglycoprotein receptor and mannose/mannose receptor is dependent upon not only pH but also calcium-ion concentration. Since most of the sugar chain receptors are C type lectins, the binding between a sugar chain receptor and a sugar chain has calcium-ion concentration dependency. More specifically, similarly to the binding between an antigen-binding molecule and an antigen, the binding between a sugar chain receptor and a sugar chain may vary depending upon the calcium-ion concentration. It is sufficient that the binding in a high calcium-ion concentration is higher than the binding in a low calcium-ion concentration.
Note that, in the present invention, when the binding activity to a sugar chain receptor (particularly a human-derived sugar chain receptor) is measured in different pH conditions, same conditions other than pH condition are preferably employed.
The present invention provides an antigen-binding molecule having an antigen-binding domain, an FcRn binding domain and one or more binding domains to a sugar chain receptor, an antigen-binding molecule increased in number of binding domains to the sugar chain receptor, and an antigen-binding molecule further containing an antigen-binding domain whose binding activity to an antigen in an acidic pH range is lower than the binding activity to the antigen in a neutral pH range. Furthermore, the present invention provides a method for producing the antigen-binding molecule and a pharmaceutical composition containing the antigen-binding molecule. Furthermore, the present invention provides a method for introducing an antigen-binding molecule and/or an antigen, to which the antigen-binding molecule is to be bound, into a cell, a method for increasing the number of antigens to which a single antigen-binding molecule binds, a method of reducing the number of antigens present outside a cell, a method for improving the pharmacokinetics of the antigen-binding molecule, and a method for promoting dissociation of an antigen from the antigen-binding molecule, comprising bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor, in-vivo or ex-vivo. Moreover, the present invention provides a method for promoting uptake of the antigen-binding molecule and/or an antigen having the antigen-binding molecule bound thereto, into a cell, a method for increasing the number of antigens to which a single antigen-binding molecule binds, in-vivo or ex-vivo, a method of enhancing a potency of the antigen-binding molecule to clear antigens in-vivo and ex-vivo, a method for improving the pharmacokinetics of the antigen-binding molecule, and a method for promoting dissociation of an antigen from the antigen-binding molecule, comprising, in an antigen-binding molecule having an antigen-binding domain, an FcRn binding domain and one or more binding domains to a sugar chain receptor, increasing the number of binding domains to the sugar-chain receptor.
The present invention provides a method for producing an antigen-binding molecule having an antigen-binding domain, an FcRn, particularly a human FcRn binding domain and one or more sugar chain receptor-binding domains, and having a binding activity to the sugar chain receptor in a neutral pH range, in which the binding activity to the sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range; and the antigen-binding activity in an acidic pH range is lower than (the antigen-binding activity) in a neutral pH range. Also, the present invention provides a method for producing an antigen-binding molecule having an excellent promotion effect in decreasing the antigen concentration in plasma and being excellent in pharmacokinetics. The present invention provides a method for producing an antigen-binding molecule, which is particularly usefully used as a pharmaceutical composition.
Specifically, the present invention provides a method for producing an antigen-binding molecule having the following steps:
(a) a step of providing a polypeptide sequence of the antigen-binding molecule containing an antigen-binding domain and an FcRn binding domain,
(b) a step of identifying an amino acid sequence serving as a candidate for a motif for a sugar chain receptor-binding domain in the polypeptide sequence,
(c) a step of designing the motif for a sugar chain receptor-binding domain containing an amino acid sequence, which contains at least one amino acid different from the amino acid sequence identified in the step (b),
(d) a step of preparing a gene encoding a polypeptide of an antigen-binding molecule containing the motif for the sugar chain receptor-binding domain designed in the step (c), and
(e) a step of recovering the antigen-binding molecule from a culture fluid of a host cell transformed with the gene obtained in the step (d).
Note that the steps (c) and (d) may be repeated two or more. The number of repeating the steps (c) and (d) is not particularly limited but usually within 10 times. As described later, a step of further treating the antigen-binding molecule obtained in the step (e) with an enzyme is also included in the method of the present invention.
The antigen-binding domain contained in the antigen-binding molecule produced by a method provided by the present invention can be provided by the method described in the section: “Antigen-binding domain”.
The FcRn binding domain having a binding activity to FcRn (particularly human FcRn) and contained in the antigen-binding molecule produced by the method provided by the present invention can be provided by a method described in the section: “FcRn-binding domain”. More specifically, the FcRn binding domain is not particularly limited as long as it has a binding activity to FcRn (particularly human FcRn) in the acidic pH range. Furthermore, a domain having a binding activity directly or indirectly to FcRn (particularly human FcRn) can be used. As such a domain, Fc region of an IgG immunoglobulin, albumin, albumin domain 3, anti-human FcRn antibody, anti-human FcRn peptide, and anti-human FcRn Scaffold molecule, which have a binding activity directly to FcRn, (particularly a human FcRn), or an IgG and albumin, which have a binding activity indirectly to human FcRn, are mentioned. In the present invention, the polypeptide sequence of a domain having a binding activity directly or indirectly to FcRn (particularly, a human FcRn) can be provided as the polypeptide sequence of the antigen-binding domain.
As an example of the sugar chain receptor-binding domain contained in the antigen-binding molecule produced by a method provided by the present invention, the sugar chain receptor-binding domain having a desired sugar chain bound thereto is preferably mentioned. As a desired sugar chain, an O-linked sugar chain or N-linked sugar chain is preferably mentioned. As a method for binding a sugar chain to a sugar chain receptor-binding domain, a known method can be employed. In one of such methods known in the art, a gene, to which a motif sequence (more specifically, a motif for a sugar chain receptor-binding domain) for adding a desired sugar chain is introduced by a genetic recombination technique, etc., and which encodes a sugar chain receptor-binding domain contained in an antigen-binding molecule present in nature or artificially produced, is introduced into a host cell, which is then cultured. From the culture fluid of the host cell, the antigen-binding molecule of the present invention containing a sugar chain receptor-binding domain, to which a desired sugar chain is to be bound, can be produced.
In a step of identifying the amino acid sequence serving as a candidate for the motif for a sugar chain receptor-binding domain in the polypeptide sequence provided as described above, for example, the following method can be used. A motif sequence to which an O-linked sugar chain is added can be identified by use of database known in the art. Furthermore, when the hinge portion of an antibody is contained in the antigen-binding molecule of the present invention, from which isotype of antibody the hinge portion is derived can be identified. Such a hinge portion can be identified as a motif candidate for the O-linked sugar chain receptor-binding domain. When the sugar chain is an N-linked sugar chain, a motif sequence (more specifically, a motif for an N-linked sugar chain receptor-binding domain) to which an N-linked sugar chain is added, is known to consist of three continuous amino acids, i.e., Asn-X-Ser/Thr. Because of this, in order to design a sugar chain receptor-binding domain so as to encode a motif for an N-linked sugar chain receptor-binding domain, i.e., Asn-X-Ser/Thr, by a genetic recombination technique, etc., the presence or absence of a sequence, which is the equivalent or analogous to Asn-X-Ser/Thr in the polypeptide sequence provided is determined.
A motif for a sugar chain receptor-binding domain containing an amino acid sequence different in at least one amino acid from the amino acid sequence identified as mentioned above can be designed. To describe more specifically, using the database etc. known in the art, an amino acid in the polypeptide sequence serving as a candidate motif sequence to which an O-linked sugar chain added and identified above is substituted to design an O-linked sugar chain motif sequence. Furthermore, when the hinge portion of an antibody is contained in the antigen-binding molecule of the present invention, if a hinge portion derived from an IgA antibody is not contained in the hinge portion, the sequence of the hinge portion is substituted with the sequence derived from an IgA antibody to design an O-linked sugar chain motif sequence. In contrast, when the sugar chain is an N-linked sugar chain, if the sequence, which is equivalent or analogous to Asn-X-Ser/Thr, is not identified in the polypeptide sequence provided, an Asn-X-Ser/Thr sequence is inserted in an appropriate site of the polypeptide sequence provided. In this manner, a new motif for an N-linked sugar chain receptor-binding domain can be added. Furthermore, if the amino acid residue of an analogous sequence to an Asn-X-Ser/Thr sequence found in the polypeptide sequence provided is substituted, the analogous sequence can be modified to the Asn-X-Ser/Thr sequence, which is a motif for an N-linked sugar chain receptor-binding domain.
The antigen-binding molecule of the present invention has one or more binding domains to a sugar chain receptor (particularly, a human sugar chain receptor). The binding domain to a sugar chain receptor (particularly a human sugar chain receptor) is not particularly limited in type and number, as long as the antigen-binding molecule has a binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range and as long as the binding activity to the sugar chain receptor in an acidic pH range is lower the binding activity to the sugar chain receptor in a neutral pH range. Furthermore, a domain having a binding activity directly or indirectly to a sugar chain receptor (particularly, a human sugar chain receptor) can be used. Examples of such a domain may include a sugar chain having direct binding activity to a sugar chain receptor (particularly, a human sugar chain receptor); an Fc domain of IgG immunoglobulin; an antibody against a sugar chain receptor (particularly, a human sugar chain receptor); a peptide that binds to a sugar chain receptor (particularly, a human sugar chain receptor); and a Scaffold molecule to a sugar chain receptor (particularly, a human sugar chain receptor). In the present invention, a sugar chain receptor-binding domain having a binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range, in which the binding activity to the sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range, is preferred. The domain can be used as it is, if it is a sugar chain receptor-binding domain already having a binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range in which the binding activity to the sugar chain receptor in an acidic pH range is lower than (the binding activity to the sugar chain receptor) in the neutral pH range. The binding activity between a sugar chain receptor-binding domain having an N-linked sugar chain having galactose at a terminal and an asialoglycoprotein receptor (sugar chain receptor-binding to the sugar chain) in an acidic pH range is preferably mentioned as an example of the case where the binding activity is lower than (the binding activity) in a neutral pH range. Furthermore, the binding activity between a sugar chain receptor-binding domain having an N-linked sugar chain having mannose at a terminal and a mannose receptor (sugar chain receptor binding to the sugar chain) in an acidic pH range is preferably mentioned as an example of the case where the binding activity is lower than (the binding activity) in a neutral pH range.
When the binding activity of a sugar chain receptor-binding domain to a sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range is zero or weak, the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) can be acquired by modifying an amino acid in the antigen-binding molecule. Alternatively, the binding activity to a sugar chain receptor (particularly, a human sugar chain receptor) can be enhanced by modifying an amino acid in the domain already having the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in a neutral pH range. With respect to modification of an amino acid in the binding domain to a sugar chain receptor (particularly, a human sugar chain receptor), a desirable modification can be found out by comparing the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the neutral pH range between before and after modification of an amino acid
The binding activity of a sugar chain receptor-binding domain to a sugar chain receptor (particularly, a human sugar chain receptor) in an acidic pH range is not lower than (the binding activity to the sugar chain receptor) (particularly, a human sugar chain receptor) in a neutral pH range, the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the acidic pH range lower than (the binding activity to the sugar chain receptor) (particularly, a human sugar chain receptor) in the neutral pH range can be acquired by modifying an amino acid in the antigen-binding molecule. With respect to modification of an amino acid in the binding domain to a sugar chain receptor (particularly, a human sugar chain receptor), a desirable modification can be found out by comparing the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the acidic pH range to the binding activity to the sugar chain receptor (particularly, a human sugar chain receptor) in the neutral pH range between before and after modification of an amino acid.
In the present invention, as long as the binding to an antigen by an antigen-binding domain is not inhibited, a sugar chain receptor-binding domain can be introduced at any site of the structure of the antigen-binding molecule. The site can be introduced in the antigen-binding domain as long as it does not inhibit the binding to an antigen by an antigen-binding domain, and can be introduced in other sites. In another aspect, as long as an sugar chain receptor-binding domain does not inhibit the binding of an FcRn binding domain of an antigen-binding molecule to FcRn (particularly human FcRn), the sugar chain receptor-binding domain can be introduced in any site of the structure of the antigen-binding molecule. For example, an IgA antibody hinge portion can be a candidate for the amino acid sequence of a sugar chain receptor-binding domain for binding an O-linked sugar chain. Asn-X-Ser/Thr (motif sequence for adding an N-linked sugar chain) can be a candidate for the amino acid sequence of a sugar chain receptor-binding domain for binding an N-linked sugar chain. If a gene encoding an antigen-binding molecule containing such an amino acid sequence is introduced into a host cell (described later) and cultured. From the culture fluid, the antigen-binding molecule of the present invention containing a sugar chain receptor-binding domain, to which a desired sugar chain is to be bound, can be produced.
In the present invention, the expression: “the binding to an antigen is not inhibited by an antigen-binding domain” means that the antigen-binding activity of an antigen-binding molecule after introduction of an sugar-chain receptor-binding domain is maintained at a level of 20% or more, preferably 50% or more, further preferably 80% or more, more preferably 90% or more of the antigen-binding activity of the antigen-binding molecule before the introduction of the sugar chain receptor-binding domain. When the antigen-binding activity of an antigen-binding molecule decreases by the introduction of a sugar chain receptor-binding domain, the antigen-binding activity can be changed to the same level as the antigen-binding activity before the sugar chain receptor-binding domain is introduced by substitution, deletion, addition and/or insertion of one or a plurality of amino acids in the antigen-binding molecule. The present invention also includes the antigen-binding molecule that regains the binding activity to the same level as that before the introduction by such a substitution, deletion, addition and/or insertion of one or a plurality of amino acids performed after the introduction of a sugar chain receptor-binding domain. Furthermore, the expression: “the binding to FcRn (particularly human FcRn) is not inhibited by a sugar chain receptor-binding domain” means that the binding activity of an antigen-binding molecule to FcRn (particularly human FcRn) after introduction of an sugar-chain receptor-binding domain is maintained at a level of 20% or more, preferably 50% or more, further preferably 80% or more, more preferably 90% or more of the binding activity of the antigen-binding molecule before the introduction of the sugar chain receptor-binding domain. When the binding activity of an antigen-binding molecule to FcRn (particularly human FcRn) decreases by the introduction of a sugar chain receptor-binding domain, the antigen-binding activity can be changed to the same level as the antigen-binding activity to FcRn (particularly human FcRn) before the sugar chain receptor-binding domain is introduced by substitution, deletion, addition and/or insertion of one or a plurality of amino acids in the antigen-binding molecule. The present invention also include the antigen-binding molecule that regains the binding activity to the same level as that before the introduction by such a substitution, deletion, addition and/or insertion of one or a plurality of amino acids performed after the introduction of a sugar chain receptor-binding domain.
Furthermore, a sugar chain receptor-binding domain can be introduced into sites other than an antigen-binding domain and an FcRn binding domain constituting an antigen-binding molecule.
In the present invention, the structure of the target antigen-binding molecule is not particularly limited, and an antigen-binding molecule having any structure can be preferably used. However, as a preferable example of the antigen-binding molecule having an antigen-binding domain, a binding domain to FcRn (particularly a human FcRn domain), and two or more sugar chain receptor domains, an antibody is mentioned. As a preferable example of the antibody of the present invention, an IgG antibody is mentioned. When an IgG antibody is used as the antibody, the type thereof is not limited and IgG isotypes (subclass) such as IgG1, IgG2, IgG3 and IgG4 can be used. Furthermore, a constant region of an antibody can be included in the antigen-binding molecule of the present invention and an amino acid mutation can be introduced in the portion of the constant region. As the amino acid mutation to be introduced, mutations that increase or decrease binding to, for example, an Fcγ receptor (Proc Natl Acad Sci USA. 1 (2006) 103 (11), 4005-10) is mentioned but the mutation is not limited to these. Furthermore, pH-dependent binding can be changed by selecting a proper constant region such as an IgG2 constant region.
When the antigen-binding molecule targeted by the present invention is an antibody, an antibody derived from any animal such as a mouse antibody, a human antibody, a rat antibody, a rabbit antibody, a goat antibody and a camel antibody, can be used. Furthermore, for example, a chimeric antibody can be used. Of the chimeric antibodies, a modified antibody prepared by substituting an amino acid sequence, such as a humanized antibody, can be preferably used. Moreover, a bispecificity antibody, a modified antibody prepared by binding various types of molecules and a polypeptide containing an antibody fragment, etc., can be used.
The “chimeric antibody” refers to an antibody prepared by combining sequences derived from different animals. As a specific examples of the chimeric antibody, an antibody, which is produced of a mouse antibody heavy chain/light chain variable (V) region and a human antibody heavy chain/light chain constant (C) region, can be mentioned.
The “humanized antibody” is also called as a reshaped human antibody, which is an antibody prepared by grafting an antibody derived from a mammalian animal except a human, for example, a mouse antibody complementarity determining region (CDR) to human antibody CDR. A method for identifying CDR is known in the art (Kabat et al., Sequence of Proteins of Immunological Interest (1987), National Institute of Health, Bethesda, Md., Chothia et al., Nature (1989) 342, 877). Furthermore, a general genetic recombination technique for this is known in the art (EP125023, WO1996/002576).
The bispecific antibody refers to an antibody having variable regions recognizing different epitopes in the same antibody molecule. The bispecific antibody can be an antibody recognizing two or more different antigens and can be an antibody recognizing two or more different epitopes on the same antigen.
As the polypeptide containing an antibody fragment, for example, an Fab fragment, an F(ab′)2 fragment, a scFv (Nat Biotechnol. (2005) 23 (9), 1126-36) domain antibody (dAb) (WO2004/058821, WO2003/002609), scFv-Fc (WO2005/037989), dAb-Fc and an Fc fusion protein are mentioned. In a molecule containing an Fc region, the Fc region can be used as a binding domain to FcRn (particularly a human FcRn domain). Furthermore, a molecule prepared by fusing a human FcRn binding domain to such a molecule can be used.
A gene encoding an antigen-binding domain designed as described above, an FcRn binding domain and a sugar chain receptor-binding domain can be prepared. A method for preparing a gene is known in the art. A gene can be prepared by a chemical synthesis and can be prepared by e.g., PCR method in which nucleotides constituting a polynucleotide are ligated in the presence of a primer (serving as a template) by an enzyme reaction. The antigen-binding domain designed as described above, an FcRn binding domain, and a sugar chain receptor-binding domain can be ligated by expressing individual domains separately in host cells (described later), collecting polypeptides from cultures fluids and performing a chemical reaction in the presence of a crosslinking agent. Examples of a synthesized chemical linker (chemical crosslinking agent) include crosslinking agents usually used in crosslinking peptides such as N-hydroxy succinimide (NHS), disuccinimidyl suberate (DSS), bis(sulfosuccineimidyl) suberate (BS3), dithiobis(succinimidylpropionate) (DSP), dithiobis(sulfosuccinimidylpropionate) (DTSSP), ethylene glycol bis(succinimidyl succinate) (EGS), ethylene glycol bis(sulfosuccinimidylsuccinate) (sulfo-EGS), disuccinimidyl tartrate (DST), disulfosuccinimidyl tartrate (sulfo-DST), bis[2-(oxysuccinimideoxycarbonyloxy)ethyl]sulfone (BSOCOES) and bis[2-(sulfosuccinimideoxycarbonyloxy)ethyl]sulfone (sulfo-BSOCOES). These crosslinking agents are commercially available.
A gene, which is designed so as to link an antigen-binding domain as designed mentioned above, an FcRn binding domain, and a sugar chain receptor-binding domain via a peptide bond in frame, is expressed in a host cell (described later). In this manner, an antibody can be obtained by collecting from a culture fluid, etc. In ligating the domains via a peptide bond in frame, the domains can be directly ligated to each other and ligated via a linker having a specific peptide sequence. As the linker for ligating the domains, any peptide linker can be used as long as it can be introduced in a genetic engineering manner or a synthesized compound linker such as a linker disclosed in the document (see, for example, Protein Engineering (1996) 9 (3), 299-305) can be used. In the present invention, a peptide linker is preferable. The length of the peptide linker, which is not particularly limited, can be appropriately selected by those skilled in the art depending upon the purpose. The length of the peptide is preferably 5 amino acids or more (the upper limit, which is not particularly limited is usually, 30 amino acids or less, preferably 20 amino acids or less) and particularly preferably 15 amino acids.
Examples of the peptide linker include:
where n is an integer of 1 or more. However, the length and sequence of a peptide linker to be used in the present invention can be appropriately selected by those skilled in the art.
The gene obtained in the production method of the present invention, is usually inserted in an appropriate vector and introduced in a host cell. The vector is not particularly limited as long as the nucleic acid inserted therein can be stably maintained. For example, if Escherichia coli is used as a host, e.g., a pBluescript vector (manufactured by Stratagene) is preferable as a cloning vector; however various commercially available vectors can be used. In order to produce the antigen-binding molecule of the present invention by use of a vector, an expression vector is particularly useful. The expression vector is not particularly limited as long as it expresses an antigen-binding molecule in-vitro, in Escherichia coli, a culture cell and an living organism. For example, a pBEST vector (manufactured by Promega KK.) is preferably used in-vitro; a pET vector (manufactured by Invitrogen) in Escherichia coli, a pME18S-FL3 vector (GenBank Accession No. AB009864) in a culture cell; and a pME18S vector (Mol Cell Biol. 8: 466-472 (1988)) in a living organism; however the expression vector is not limited to these. The gene of the present invention can be inserted into a vector by a conventional method, for example, by a ligase reaction using restriction enzyme sites (Current protocols in Molecular Biology edit. Ausubel et al. (1987) Publish. John Wiley & Sons. Section 11.4-11.11).
The host cell is not particularly limited and various host cells can be used depending upon the purpose. Examples of a cell for expressing an antigen-binding molecule include bacteria cells (example: Streptococcus, Staphylococcus, Escherichia coli, Streptomyces, Bacillus subtilis), Eumycetes cells (example: Yeast, Aspergillus), insect cells (example: Drosophila S2, Spodoptera SF9), animal cells (example: CHO, COS, HeLa, C127, 3T3, BHK, HEK293, Bowes melanoma cell) and plant cells. A vector is introduced into a host cell by a method known in the art such as a calcium phosphate precipitation method, electroporation (Current protocols in Molecular Biology edit. Ausubel et al. (1987) Publish. John Wiley & Sons. Section 9.1-9.9), a lipofection method and a micro injection method.
A host cell can be cultured by a method known in the art. For example, when an animal cell is used as a host, for example, DMEM, MEM, RPMI1640, IMDM can be used as a culture solution. At this time, cells can be cultured in a culture using a serum replenisher such as FBS and fetal bovine serum (FCS) in combination or a serum-free medium. The pH during culture can be appropriately selected from approximately 6 to 8 but not limited to this. Various pH values can be appropriately selected depending upon the culture or culturing period/culturing time. Culture is usually performed at approximately 30 to 40° C. for approximately 15 to 200 hours and, if necessary, the medium is exchanged and aeration and stirring are performed.
To secrete an antigen-binding molecule expressed in a host cell to a lumen of endoplasmic reticulum, periplasmic space or extracellular environment, an appropriate secretion signal is integrated into a desired polypeptide. The signal may be an endogenic signal or a xenogeneic signal for a desired antigen-binding molecule.
As the system in which a polypeptide is produced, in vivo, for example, a production system using an animal and a production system using a plant are mentioned. A desired gene is inserted into a vector, which is introduced into an animal or a plant cell, and then the polypeptide encoded by the gene is expressed and recovered from the body fluid or a living body. The “host” in the present invention includes these animals and plants.
In the production system using an animal as a host, a mammalian animal and an insect are used. Examples of the mammalian animal include goat, pig, sheep, mouse and cow (Vicki Glaser, SPECTRUM Biotechnology Applications (1993)). When a mammalian animal is used, a transgenic animal can be appropriately used.
For example, a polynucleotide encoding the antigen-binding molecule of the present invention is fused with a gene encoding a polypeptide such as goat β casein (which is intrinsically produced in goat milk) to prepare a fusion gene. Subsequently, a polynucleotide fragment containing the fusion gene is injected into a goat embryo and the embryo is grafted in a female goat. The goat to which the embryo is grafted, gives birth a transgenic goat. From the milk of the transgenic goat and its progenies, a desired antigen-binding molecule can be collected. To increase the amount of milk produced from a transgenic goat and containing the antigen-binding molecule, an appropriate hormone can be administered to the transgenic goat (Ebert et al., Bio/Technology (1994) 12, 699-702).
As an insect for producing the antigen-binding molecule of the present invention, for example, a silk worm can be used. When a silk worm is used, a polynucleotide encoding a desired antigen-binding molecule is inserted into a baculovirus and then a silk worm is infected with the baculovirus. A desired antigen-binding molecule can be collected from the body fluid of the silk worm.
When a plant is used for producing the antigen-binding molecule of the present invention, for example, tobacco can be used. When tobacco is used, a polynucleotide encoding a desired antigen-binding molecule is inserted into a plant expression vector such as pMON 530, which is then introduced into a bacterium such as Agrobacterium tumefaciens. Tobacco is infected with the bacterium. From the leaves of the tobacco, a desired antigen-binding molecule can be recovered (Ma et al., Eur. J. Immunol. (1994) 24, 131-8). Furthermore, duckweed (Lemna minor) is infected with the bacterium. From clone cells of duckweed, a desired antigen-binding molecule can be recovered (Cox K M et al. Nat. Biotechnol. (2006) (12), 1591-1597).
When the sugar chain receptor-binding domain having a desired sugar chain bound thereto is used as a sugar chain receptor-binding domain contained in the antigen-binding molecule in the present invention, a method known in the art can be employed as a method for binding a sugar chain to a sugar chain receptor-binding domain. For example, an enzymatic method performed in an acellular system as described in (Japanese Patent Laid-Open No. 2006-141241), which is a method for producing an antibody modified after translation in an acellular protein synthesis system, comprising preparing a cell extraction solution from cultured cells of an immortalized mammalian animal cell strain capable of secreting a protein and adding mRNA encoding an antibody to the extraction solution, can be employed as a method for producing the sugar chain receptor-binding domain having a desired sugar chain bound thereto. Such an antigen-binding molecule may be further treated with an enzyme. This step can be included in the method of the present invention.
The antigen-binding molecules produced as mentioned above may have the same sugar chain structure in some cases; whereas, the antigen-binding molecules are produced as a mixture of the antigen-binding molecules having different sugar chains added thereto in other cases. In the present invention, such a mixture can be also preferably used. Furthermore, an antigen-binding molecule having a sugar-chain binding-domain to which a specific sugar chain is connected can be preferably used in the present invention.
As a method for connecting a specific sugar chain to a sugar chain receptor-binding domain contained in the antigen-binding molecule in the present invention, a plurality of methods known in the art can be employed. As one of the known methods, a method of purifying an antigen-binding molecule having a specific sugar chain by use of a property of a sugar chain of a natural antigen-binding molecule or an artificial antigen-binding molecule (prepared by a genetic recombination method, etc.) is mentioned. An antibody having high-mannose sugar chain is known to be purified by affinity chromatography using ConA-sepharose (Millward (Biologicals (2008) 36, 49-60)). Such a purification method can be used for preparing an antigen-binding molecule having an N-linked sugar chain having mannose at the non-reducing end, in the present invention
As necessary, before and after purification of an antigen-binding molecule, an appropriate protein modification enzyme may be used. In this manner, modification can be optionally added or a molecule such as a peptide used for partial or entire modification can be removed. Examples of the protein modification enzyme that can be used include trypsin, chymotrypsin, Lysyl Endopeptidase, protein kinase and glucosidase. The antigen-binding molecule may be further treated with an enzyme. Such an enzymatic treatment step is also included in the method of the present invention.
As a method for ligating a specific sugar chain to a sugar chain receptor-binding domain contained in the antigen-binding molecule of the present invention, a plurality of methods known in the art can be employed. In order to obtain an antigen-binding molecule having a specific sugar chain, an enzyme treatment can be appropriately employed. As described later in Examples, an antigen-binding molecule having an N-linked sugar chain having galactose at a terminal can be prepared from an antigen-binding molecule having a complex sugar chain having sialic acid at a terminal, by a sialidase treatment. Furthermore, it is known that an antibody having a high-mannose sugar chain from which galactose is removed is prepared by sialidase and β galactosidase treatment (Newkirk (Clin. Exp. Immunol. (1996) 106, 259-264)). Such a preparation method including treatments with sialidase and β galactosidase can be used for preparing an antigen-binding molecule having an N-linked sugar chain having mannose at a terminal, in the present invention. The antigen-binding molecule may be further treated with an enzyme. Such an enzymatic treatment step is also included in the production method of the present invention.
Through introduction into a host cell as described later, the antigen-binding molecule of the present invention containing a sugar chain receptor-binding domain (to which a desired sugar chain is to be bound) can be produced from the culture fluid of the host cell.
In a different aspect, in order to obtain an antigen-binding molecule having a specific sugar chain of the present invention, a method including transfecting a host cell with a recombinant gene encoding the antigen-binding molecule, modifying glycosidase activity of the host cell so as to accumulate a specific sugar chain (by a method including genetic or genetic recombination technique but not limited to these), and recovering the antigen-binding molecule from a culture fluid of the host cell, can be appropriately employed. It is known that an antibody having a high mannose N-linked sugar chain is collected from a culture fluid of a Lec1 mutation strain derived from a CHO cell defective in N-acetylglucosaminyltransferase I activity and transfected with a recombinant gene encoding the antibody (Wright and Morrison (J. Exp. Med. (1994) 180, 1087-1096)). In the present invention, an antigen-binding molecule having an N-linked sugar chain (having mannose at the non-reducing end) can be collected from a culture fluid of a Lec1 mutation strain transfected with a recombinant gene encoding the antigen-binding molecule.
In another aspect, in order to obtain an antigen-binding molecule having a specific sugar chain of the present invention, a method including culturing a cell producing the antigen-binding molecule with the addition of an inhibitor for a specific glycosidase reaction and collecting an antigen-binding molecule having a specific sugar chain accumulated in the culture fluid can be appropriately employed. It is known that an antibody having a high mannose N-linked sugar chain without fucose is collected from a culture fluid of a CHO cell producing the antibody cultured with the addition of kifunesine (Zhou (Biotechnol. Bioeng. (2008) 99, 652-665)). 652-665)). In the present invention, an antibody having an N-linked sugar chain having mannose at a terminal without fucose can be collected from a culture fluid of a CHO cell transfected with a recombinant gene encoding the molecule and cultured with the addition of kifunesine. Furthermore, the antigen-binding molecule having a specific sugar chain of the present invention can be obtained by using a method of adding such an inhibitor in combination in culturing a host cell whose glycosidase activity is modified as mentioned above. It is known that an antibody having a specific sugar chain can be collected by such a combination (Kanda, et al. (Glycobiology (2007) 17, 104-118)). In the present invention, in order to obtain an antigen-binding molecule having a specific sugar chain, the same combination can be appropriately employed.
The antigen-binding molecules produced as mentioned above may have the same sugar chain structure in some cases; whereas, the antigen-binding molecules are produced as a mixture of the antigen-binding molecules having different sugar chains added thereto in other cases. In the present invention, such a case of a sugar chain mixture can be preferably used. Furthermore, an antigen-binding molecule having a sugar-chain binding-domain (to which a specific sugar chain is connected) can be preferably used in the present invention.
The antigen-binding molecule thus obtained is isolated from a host cell or outside the cell (medium, milk, etc.) and can be purified as a substantially pure and homogeneous antigen-binding molecule. The method for separating and purifying used for separation and purification of the antigen-binding molecule can be appropriately selected from conventional separation and purification methods (these methods may be used in combination depending upon the purpose); but is not limited to a specific method. Examples thereof include column chromatography, filtration, ultrafiltration, salting out, solvent deposition, solvent extraction, distillation, immunoprecipitation, SDS-polyacrylamide gel electrophoresis, isoelectric focusing, dialysis and recrystallization. These may be appropriately selected or used in combination for separating and purifying an antigen-binding molecule.
Examples of the chromatography include affinity chromatography, ion exchange chromatography, hydrophobic chromatography, gel filtration, reverse phase chromatography, and adsorption chromatography (Strategies for Protein Purification and Characterization: A Laboratory Course Manual. Ed Daniel R. Marshak et al. (1996) Cold Spring Harbor Laboratory Press). These chromatographic methods can be performed by use of liquid phase chromatography such as HPLC, FPLC. As the column to be used in affinity chromatography, a protein A column and a protein G column are mentioned. For example of a column using protein A, Hyper D, POROS, and Sepharose F. F. (manufactured by Pharmacia), etc. are mentioned.
Whether the antigen-binding molecule prepared as mentioned above has an antigen-binding activity to FcRn (particularly human FcRn) and a desired sugar chain receptor binding activity, etc. or not is evaluated by the method of determining an antigen-binding activity, an FcRn-binding activity or an sugar chain receptor-binding activity as mentioned above. As a result of the evaluation, a step of designing a motif for a sugar chain receptor-binding domain and a step of preparing a gene encoding a polypeptide of an antigen-binding molecule containing a motif for a sugar chain receptor-binding domain are repeated more than once to obtain an antigen-binding molecule having a desired property.
An antigen-binding molecule containing a sugar chain receptor-binding domain (particularly a human derived sugar chain receptor-binding domain) according to the present invention binds to a sugar chain receptor in a pH-dependent manner and/or, having a sugar chain receptor-binding activity (particularly a human-derived sugar chain receptor-binding activity) in a neutral pH range. If the binding activity to a sugar chain receptor in an acidic pH range can be lowered than (the binding activity to the sugar chain receptor) in the neutral pH range property, the uptake of an antigen into a cell by the antigen-binding molecule can be promoted. If such an antigen-binding molecule is administered, a decrease of the antigen concentration in plasma can be promoted and the pharmacokinetics of the antigen-binding molecule can be improved, with the result that the number of antigens that can be bound by a single antigen-binding molecule can be increased.
The antigen-binding molecule produced by the production method of the present invention is an antigen-binding molecule that can promote a decrease of the antigen concentration in plasma by administration. Therefore, the production method of the present invention can be used as a method for producing an antigen-binding molecule, by administration of which the antigen concentration in plasma is promoted.
The antigen-binding molecule produced by the production method of the present invention is an antigen-biding molecule improved in pharmacokinetics. Therefore, the production method of the present invention can be used as a method for producing an antigen-binding molecule improved in pharmacokinetics.
It is considered that the antigen-binding molecule produced by the production method of the present invention can increase the number of antigens that can be bound by a single antigen-binding molecule by administering it to an animal such as a human, a mouse and a monkey. Therefore, the production method of the present invention can be used for producing an antigen-binding molecule capable of binding to a larger number of antigens per molecule.
It is considered that when the antigen-binding molecule produced by the production method of the present invention is administered to an animal such as a human, a mouse and a monkey and binds to an antigen outside the cell, the antigen can be dissociated from the antigen-binding molecule within the cell. Therefore, the production method of the present invention can be used as a method for producing an antigen-binding molecule capable of intracellularly dissociating an antigen extracellularly bound.
It is considered that when the antigen-binding molecule produced by the production method of the present invention is administered to an animal such as a human, a mouse and a monkey and binds to an antigen, the antigen-binding molecule bound to the antigen can be taken up into a cell and then released as a free antibody (without an antigen attached thereto). The production method of the present invention can be used as a method for producing an antigen-binding molecule, which is taken up into a cell while binding to an antigen and released outside the cell as a free antigen-binding molecule (not attached with the antigen).
When such an antigen-binding molecule is administered, it highly effectively reduce the antigen concentration in plasma compared to a conventional antigen-binding molecule. Therefore, it is considered that the antigen-binding molecule is particularly excellent as a pharmaceutical product. Therefore, the production method of the present invention can be used as a method for producing an antigen-binding molecule for use in a pharmaceutical composition.
The present invention also relates to a pharmaceutical composition containing the antigen-binding molecule of the present invention or an antigen-binding molecule produced by the production method of the present invention. The antigen-binding molecule of the present invention or the antigen-binding molecule produced by the production method of the present invention is highly effectively reducing the antigen concentration in plasma by administration thereof, compared to a conventional antigen-binding molecule. Therefore, antigen-binding molecule of the present invention is useful for use in a pharmaceutical composition. The pharmaceutical composition of the present invention can contain a pharmaceutically acceptable carrier.
In the present invention, the pharmaceutical composition generally refers to a medicinal agent for treating or preventing a disease or examination/diagnosis.
The pharmaceutical composition of the present invention can be prepared by a method known to those skilled in the art. The pharmaceutical composition of the present invention is mixed with, for example, water or a pharmaceutically acceptable liquid other than water to prepare an aseptic solution or an injection of a suspension agent and can be parenterally used. For example, the pharmaceutical composition of the present invention is appropriately mixed with a pharmacologically acceptable carrier or a medium, more specifically, appropriately blended with sterile water and physiological saline, a vegetable oil, an emulsifier, a suspending agent, a surfactant, a stabilizer, a flavor agent, an excipient, a vehicle, a preservative and a binder, etc. into a preparation in the form of unit dosage required for preparation practice generally admitted. The amount of active ingredient in the preparation is set so as to obtain an appropriate dose within a determined range.
An aseptic composition for an injection can be formulated in accordance with a conventional preparation practice by use of a vehicle such as distillation water for injection. As an aqueous solution for an injection, for example, an isotonic liquid including physiological saline, glucose and other additives (for example, D-sorbitol, D-mannose, D-mannitol, sodium chloride) is mentioned. An appropriate solubilizing agent such as an alcohol (ethanol, etc.), a polyalcohol (propylene glycol, polyethylene glycol, etc.) and a nonionic surfactant (polysorbate 80 (TM), HCO-50, etc.) can be used in combination.
As an oily liquid, sesame oil and soybean oil are mentioned. As a solubilizing agent, benzyl benzoate and/or benzyl alcohol can be used in combination. Furthermore, a buffer (for example, a phosphate buffer solution and a sodium acetate buffer solution), a soothing agent (for example, procaine hydrochloride), a stabilizer (for example, benzyl alcohol and phenol) and an antioxidant can be added. The injection prepared is usually charged in an appropriate ample.
The pharmaceutical composition of the present invention is preferably parenterally administered. The pharmaceutical composition of the present invention can be prepared, for example, as injectable, transnasal administration, pulmonary administration and transdermal administration compositions. The pharmaceutical composition of the present invention is administered systemically or locally, through e.g., intravenous injection, intramuscular injection, intraperitoneal injection and hypodermic injection.
As the administration method for the pharmaceutical composition of the present invention, a preferable method is appropriately selected depending upon the age and symptom of a patient. The dose of a pharmaceutical composition containing an antigen-binding molecule can be set to fall, for example, within the range of 0.0001 mg to 1000 mg per body weight (1 kg) per time or within the range of 0.001 to 100000 mg per patient. However, the dose of the pharmaceutical composition of the present invention is not always limited to these numerical values. Dose and administration method vary depending upon the weight, age and symptom, etc. of a patient. Those skilled in the art can set an appropriate dose and administration method in consideration of these conditions.
Note that amino acids contained in the amino acid sequence described in the present invention are sometimes modified after translation (for example, N-terminal glutamine is modified into pyroglutamine acid, as is known well to those skilled in the art). Such a modified antigen-binding molecule after translation is included within the range of the antigen-binding molecule specified by the amino acid sequence described in the present invention.
Method for Promoting Uptake of an Antigen-Binding Molecule or an Antigen Binding to the Antigen-Binding Molecule, Including Bringing it into Contact with a Cell Expressing a Sugar Chain Receptor In-Vivo or Ex-Vivo
The present invention further provides a method for promoting uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) into a cell, comprising bringing the antigen-binding molecule or the antigen (binding to the antigen-binding molecule) into contact with a cell expressing a sugar chain receptor, which binds to a sugar chain receptor-binding domain contained in the antigen-binding molecule, in-vivo or ex-vivo.
In the present invention, “uptake . . . into a cell” refers to uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) into a cell by endocytosis. In the present invention, the expression “promoting uptake . . . into a cell” refers to increasing a speed of taking up an antigen-binding molecule, which binds to an antigen outside a cell, into the cell. Accordingly, in the present invention, whether or not uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) was promoted is determined based on whether or not the uptake speed of the antigen-binding molecule or the antigen (binding to the antigen-binding molecule) into the cell increased or not. The uptake speed of an antigen into a cell can be calculated, for example, by adding an antigen-binding molecule and an antigen to a culture fluid containing a sugar chain receptor expression cell; and measuring a decrease of concentration of the antigen-binding molecule or the antigen (binding to the antigen-binding molecule) in the culture fluid with the passage of time, or, measuring the amount of antigen-binding molecule or antigen (binding to the antigen-binding molecule) taken up into a sugar chain receptor expression cell versus time. The contact between a cell expressing a sugar chain receptor and an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) may also occur ex-vivo as mentioned above and occurs in vivo by administering an antigen-binding molecule.
The clearance speed of an antigen in plasma can be increased by the method (provided by the present invention) for increasing an uptake speed of an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) into a cell, comprising bringing the antigen-binding molecule and the antigen (binding to the antigen-binding molecule) into contact with a cell expressing a sugar chain receptor, which binds to the sugar chain receptor-binding domain contained in the antigen-binding molecule, in-vivo or ex-vivo; more specifically by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body; or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body, can be also used. Accordingly, whether or not uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) into a cell was promoted can be confirmed also by determining whether or not the clearance speed of the antigen present in the plasma was accelerated, compared to the case where the antigen-binding molecule is not administered or by determining whether or not the concentration of the antigen in plasma was reduced by the ex-vivo method or administration of an antigen-binding molecule.
Whether uptake is promoted or not can be confirmed by determining whether or not the clearance speed of an antigen in plasma (which is determined by the above (1) and (2) methods) is accelerated compared to the clearance speed of an antigen in plasma, which is determined by the same method as above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
The present invention further provides a method of promoting uptake of an antigen binding to an antigen-binding molecule, into a cell, comprising, bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor (which binds to a sugar chain receptor-binding domain contained in the antigen-binding molecule) containing an antigen-binding domain whose binding activity to the antigen changes depending upon the ion-concentration condition, in-vivo or ex-vivo. The present invention further provides a method of promoting uptake of an antigen binding to an antigen-binding molecule into a cell, comprising, bringing the antigen-binding molecule into contact with a cell expressing a sugar chain receptor which binds to a sugar chain receptor-binding domain contained in the antigen-binding molecule containing an antigen-binding domain (whose binding activity to the antigen has been changed depending upon the ion-concentration condition), in-vivo or ex-vivo. The present invention further provides a method of promoting uptake of an antigen binding to an antigen-binding molecule into a cell, comprising bringing the antigen-binding molecule (in which at least one amino acid of an antigen-binding domain is an amino acid which changes the binding activity of the antigen-binding domain to the antigen depending upon the calcium-ion concentration condition or pH condition) into contact with a cell expressing a sugar chain receptor (which binds to a sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo.
In the present invention, as the method for “changing the binding activity of the antigen-binding domain to the antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
In the present invention, as the cell expressing a sugar chain receptor binding to a sugar chain receptor-binding domain and contained in the antigen-binding molecule, any cell can be used as long as the cell expresses a desired sugar chain receptor. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell, which is to be brought into contact with the antigen-binding molecule of the present invention, expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are also known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is, for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
Method for Increasing the Number of Antigens to which a Single Antigen-Binding Molecule Binds, Comprising Bringing an Antigen-Binding Molecule into Contact with a Cell Expressing a Sugar Chain Receptor, In-Vivo or Ex-Vivo
The present invention provides a method of increasing the number of antigens to which a single antigen-binding molecule binds, comprising bringing an antigen-binding molecule having an antigen-binding domain, an FcRn binding domain and one or more sugar chain receptor-binding domains into contact with a cell expressing a sugar chain receptor binding to the sugar chain receptor-binding domain contained in the antigen-binding molecule, in-vivo or ex-vivo.
In the present invention, the expression “the number of antigens to which a single antigen-binding molecule binds” refers to the number of antigens to which the antigen-binding molecule can bind until it is decomposed and cleared. In the present invention, “increasing the number of antigens to which a single antigen-binding molecule can bind” refers to increasing the binding times of an antigen-binding molecule which repeats dissociation from an antigen molecule and association with another antigen molecule. The antigen molecule binding to an antigen-binding molecule may be the same antigen molecule or a different antigen molecule in a reaction system where both molecules are present. In other words, the binding times refers to the total binding times of an antigen-binding molecule to an antigen in the reaction system. In other expression, provided that a process where the antigen-binding molecule bound to an antigen is taken up into a cell, dissociates the antigen in an endosome and returns outside the cell is regarded as one cycle, the number of cycle repeats until the antigen-binding molecule is decomposed and cleared is referred to the binding times. The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range binds to the sugar chain receptor and then is taken up into the cell expressing the sugar chain receptor by endocytosis. The antigen-binding molecule of the present invention is released from the sugar chain receptor in an acidic range, binds to FcRn (particularly human FcRn) in the acidic range and is recycled outside the cell. The antigen-binding molecule of the present invention, from which an antigen is dissociated in the acidic range, is recycled outside the cell. Therefore, the antigen-binding molecule can bind again to an antigen. Accordingly, whether the number of cycles increases can be determined based on whether “uptake into a cell is promoted” or not, or whether “pharmacokinetics is improved” (described later) or not.
The clearance speed of an antigen in plasma can be increased by the method (provided by the present invention) for increasing the number of antigens to which a single antigen-binding molecule binds, comprising bringing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) into contact with to a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), more specifically, by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body, or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used. Accordingly, whether or not the number of antigens to which a single antigen-binding molecule binds was increased can be confirmed also by determining whether or not the clearance speed of the antigen present in plasma has been accelerated compared to the case where the antigen-binding molecule is not administered or by determining whether or not the concentration of the antigen in plasma has been reduced by the ex-vivo method or administration of the antigen-binding molecule.
Whether the number of antigens to which a single antigen-binding molecule binds is increased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
The present invention further provides a method of increasing the number of antigens, to which a single antigen-binding molecule can bind, comprising, bringing an antigen-binding molecule, whose binding activity to an antigen changes depending upon the ion-concentration condition and thus capable of binding a larger number of antigens (in terms of the number of antigens to which a single antigen-binding molecule can bind) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), in-vivo or ex-vivo. The present invention further provides a method of increasing the number of antigens, to which a single antigen-binding molecule can bind, comprising, bringing an antigen-binding molecule containing an antigen-binding domain (whose binding activity to the antigen has been changed depending upon the ion-concentration condition and thus capable of binding a larger number of antigens (in terms of the number of antigens to which a single antigen-binding molecule can bind)), into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain) contained in the antigen-binding molecule, in-vivo or ex-vivo. The present invention further provides a method of increasing the number of antigens, to which a single antigen-binding molecule can bind, comprising bringing an antigen-binding molecule (in which at least one amino acid of the antigen-binding domain is an amino acid which changes the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition) increased in the number of antigens to which a single antigen-binding molecule can bind into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain) contained in the antigen-binding molecule, in-vivo or ex-vivo.
In the present invention, as the method of “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell (which is brought into contact with the antigen-binding molecule of the present invention) expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is, for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
Method for Decreasing the Number of Antigens Present Outside a Cell, Comprising Bringing an Antigen-Binding Molecule into Contact with a Cell Expressing a Sugar Chain Receptor In-Vivo or Ex-Vivo
The present invention provides a method of decreasing the number of antigens present outside a cell, comprising bringing an antigen-binding molecule having an antigen-binding domain, an FcRn binding domain and one or more sugar chain receptor-binding domains into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo.
The expression: the antigen present outside a cell, refers to an antigen present outside the cell expressing a sugar chain receptor. When the cell expressing a sugar chain receptor is present inside a living body, an antigen present outside the cells of a body fluid such as blood, plasma, serum, urine, lymph fluid, saliva and tear can be mentioned as an example (of the antigen present outside a cell). However, as long as the antigen-binding molecule of the present invention administered to a living body can bind to the antigen outside the cell expressing a sugar chain receptor, the antigen present outside a cell is not limited to the antigen present in these body fluids. Particularly preferable example of the antigen present outside a cell is an antigen present in plasma. When a cell expressing a sugar chain receptor is present outside a living body, not only the antigen present in a body fluid taken out from a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear, but also an antigen present in a culture fluid of the cell can be mentioned as an example of the antigen present outside a cell.
The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range, binds to the sugar chain receptor and thereafter is taken up into the cell expressing the sugar chain receptor by endocytosis. The antigen-binding molecule (of the present invention) is released from the sugar chain receptor in an acidic range and binds to FcRn (particularly human FcRn) in the acidic range. In this manner, the antigen-binding molecule of the present invention is returned again outside the cell for recycle use. The antigen-binding molecule of the present invention (from which an antigen dissociates in the acidic range) returned outside the cell for recycle use can bind again to an antigen. In this case, the antigen dissociated is decomposed in a lysosome within a cell. Therefore, every time the antigen-binding molecule of the present invention is recycled, the antigen, which is present outside the cell expressing a sugar chain receptor (which is to be bound to the antigen-binding molecule of the present invention) is decomposed in a lysosome within the cell (expressing a sugar chain receptor). As a result of such decomposition of the antigen, the number of antigens present outside the cell presumably decreases. Whether the number of antigens present outside a cell decreased or not can be evaluated by measuring the amount of antigen extracellularly present out of a body fluid such as blood, plasma, serum, urine, lymph fluid, saliva and tear if a cell (expressing a sugar chain receptor) is present within a living body, and evaluated by measuring the amount of antigen present in not only a body fluid taken out of a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear but also a culture fluid of the cell, if the cell (expressing a sugar chain receptor) is present outside a living body.
The number of antigens present outside a cell can be decreased by the method (provided by the present invention) for decreasing the number of antigens present outside a cell, comprising bringing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), in-vivo or ex-vivo, more specifically by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body; or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used. Accordingly, whether or not the number of antigens present outside a cell decreased can be confirmed also by determining whether or not the amount of antigen present in the plasma has decreased compared to the case where the antigen-binding molecule is not administered or by determining whether or not the concentration of the antigen in plasma has been reduced by the ex-vivo method or administration of an antigen-binding molecule.
Whether the amount of antigen in plasma decreased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
The present invention further provides a method of decreasing the number of antigens present outside a cell, comprising, bringing the antigen-binding molecule of the present invention containing an antigen-binding domain, whose binding activity to an antigen changes depending upon the ion-concentration condition, into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), in-vivo or ex-vivo. The present invention further provides a method of decreasing the number of antigens present outside a cell, comprising, bringing the antigen-binding molecule of the present invention containing an antigen-binding domain, whose binding activity to an antigen has been changed depending upon the ion-concentration condition, into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), in-vivo or ex-vivo. The present invention further provides a method of decreasing the number of antigens present outside a cell, comprising, bringing the antigen-binding molecule of the present invention into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule), in-vivo or ex-vivo, (in which at least one amino acid of the antigen-binding domain is an amino acid which changes the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition).
In the present invention, as the method for “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell (which is brought into contact with the antigen-binding molecule of the present invention) expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is, for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
Method for Improving the Pharmacokinetics of an Antigen-Binding Molecule, Comprising Bringing an Antigen-Binding Molecule into Contact with a Cell Expressing a Sugar Chain Receptor, In-Vivo
The present invention provides a method of improving the pharmacokinetics of an antigen-binding molecule, comprising bringing an antigen-binding molecule (having an antigen-binding domain, an FcRn binding domain and one or more sugar chain receptor-binding domains) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo.
In the present invention, “improvement of pharmacokinetics”, “enhancement of pharmacokinetics” or “excellent pharmacokinetics” can be rephrased by “improvement of retentivity in plasma (in blood)”, “enhancement of retentivity in plasma (in blood)”, “excellent retentivity in plasma (in blood)” or “extending retentivity in plasma (in blood)”. The meanings of these expressions are all the same.
In the present invention, “pharmacokinetics is improved” refers to not only extending the time period from administration of an antigen-binding molecule to a human or an animal (such as mouse, rat, monkey, rabbit and dog) up to clearance from plasma (for example, until the antigen-binding molecule is, e.g., decomposed in a cell and cannot return to the plasma) but also extending the time period during which the antigen-binding molecule remains in plasma while keeping the state capable of binding to an antigen (e.g., the state of an antigen-binding molecule not binding to an antigen) from administration of an antigen-binding molecule up to clearance from plasma by decomposition. In short, extending the time period until an antigen-binding molecule unbound to an antigen (antigen-unbound antigen-binding molecule) disappears by decomposition is included. Even if an antigen-binding molecule is present in plasma, if an antigen is already bound to the antigen-binding molecule, the antigen-binding molecule cannot bind to another antigen. Thus, if the time period during which an antigen-binding molecule is not bound to an antigen becomes long, the time period during which the antigen-binding molecule can bind to another antigen becomes long (chance to bind another antigen is increased). As a result, the time period during which an antigen is not bound to an antigen-binding molecule in vivo can be reduced and the time period during which an antigen binds to an antigen-binding molecule can be extended. If clearance of an antigen from plasma can be accelerated by administration of an antigen-binding molecule, the plasma concentration of the antigen-unbound antigen-binding molecule increases and the time period during which an antigen is bound to an antigen-binding molecule increases. In short, in the present invention, the expression: “improvement of the pharmacokinetics of an antigen-binding molecule” refers to improvement of any one of pharmacokinetics parameters of an antigen-unbound antigen-binding molecule (any one of the parameters: an increase of half-life period in plasma, an increase of average retention time in plasma and decrease of clearance in plasma), or extension of time period during which an antigen is bound to an antigen-binding molecule after the antigen-binding molecule is administered, or acceleration of antigen clearance from plasma by an antigen-binding molecule. Determination can be made by measuring any one of parameters (understanding of pharmacokinetics, by practice (Nanzando Co., Ltd.)): half-life period of an antigen-binding molecule or an antigen-unbound antigen-binding molecule in plasma, average retention time in plasma and clearance in plasma. For example, when an antigen-binding molecule is administered to a mouse, rat, monkey, rabbit, dog and human, etc. the concentration of antigen-binding molecule (or antigen-unbound antigen-binding molecule) in plasma is measured and individual parameters are calculated. For example, if the half-life period in plasma extends or if the average retention time in plasma extends, it is evaluated that the pharmacokinetics of the antigen-binding molecule is improved. These parameters can be measured by a method known to those skilled in the art and can be appropriately evaluated by Noncompartmental analysis using, e.g., pharmacokinetics analysis soft WinNonlin (Pharsight) in accordance with the accompanying protocol. The concentration of an antigen-unbound antigen-binding molecule in plasma can be measured by a method known to those skilled in the art. For example, a measurement method employed in Clin Pharmacol. (2008) 48 (4) 406-17 can be used.
In the present invention, the concept: “pharmacokinetics is improved” includes extending the time period during which antigen binds to an antigen-binding molecule after administration of the antigen-binding molecule. Whether the time period during which an antigen binds to an antigen-binding molecule after administration of the antigen-binding molecule is extended or not can be determined by measuring the concentration of an antigen-binding molecule-unbound antigen (antigen not binding to an antigen-binding molecule) in plasma, more specifically, based on the time until the concentration of antigen-binding molecule-unbound antigen in plasma or the rate of the concentration of an antigen-binding molecule-unbound antigen relative to total antigen concentration increases.
The concentration of antigen-binding molecule-unbound antigen in plasma or the rate of the concentration of an antigen-binding molecule-unbound antigen relative to total antigen concentration can be determined by a method known to those skilled in the art. For example, the measurement method described in Pharm Res. (2006) 23 (1) 95-103 can be used. When an antigen plays some role in-vivo, whether or not the antigen has bound to an antigen-binding molecule (antagonist molecule), which neutralizes the function of the antigen, can be evaluated by determining whether or not the function of the antigen has been neutralized. Whether or not the function of the antigen is neutralized can be evaluated by measuring any one of in-vivo markers which reflect the function of the antigen. Whether or not an antigen binds to an antigen-binding molecule (agonist molecule) activating the function of the antigen, can be evaluated by measuring an in-vivo marker which reflects the function of the antigen.
Measurement, such as measurement of the concentration of plasma of an unbound antigen, measurement of the ratio of the amount of unbound antigen relative to the total antigen amount and measurement of in-vivo marker, is not particularly limited and preferably performed after a lapse of predetermined time from administration of an antigen-binding molecule. In the present invention, the time period expressed by the phrase: after a lapse of a predetermined time from administration of an antigen-binding molecule is not particularly limited, and can be appropriately determined by those skilled in the art in consideration of the properties of the antigen-binding molecule to be administered. For example, one day, 3 days, 7 days, 14 days and 28 days after an antigen-binding molecule is administered are mentioned.
In the present invention, it is preferable that pharmacokinetics in a human is improved. If it is difficult to measure retentivity in plasma in a human, retentivity in plasma in a human can be estimated based on retentivity in plasma of a mouse (for example, normal mouse, human antigen expression transgenic mouse, human FcRn expressing transgenic mouse 32 lineage or 276 lineage (Jackson Laboratories) (Methods Mol Biol. (2010) 602, 93-104) etc., transgenic mouse, etc.) and a monkey (for example, crab-eating monkey).
Furthermore, the present invention provides a method of improving pharmacokinetics of an antigen-binding molecule, comprising administering the antigen-binding molecule, in-vivo, whose pharmacokinetics is improved as mentioned above and which contains an antigen-binding domain, whose binding activity to an antigen changes depending upon the ion-concentration condition. The present invention further provides a method of improving pharmacokinetics of an antigen-binding molecule, comprising administering an antigen-binding molecule, in-vivo, whose pharmacokinetics is improved as mentioned above and which contains an antigen-binding domain, whose binding activity to an antigen has been changed depending upon the ion-concentration condition. The present invention further provides a method of improving pharmacokinetics of an antigen-binding molecule, comprising administering the antigen-binding molecule (in which at least one amino acid of the antigen-binding domain is an amino acid which changes the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition and whose pharmacokinetics is improved) in-vivo.
In the present invention, as a method for “changing the binding activity of the antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Method for Promoting Dissociation of an Antigen from Antigen-Binding Molecule within a Cell, Including Bringing Antigen-Binding Molecule to a Cell Expressing a Sugar Chain Receptor, In-Vivo or Ex-Vivo
The present invention provides a method for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell, comprising bringing an antigen-binding molecule (having an antigen-binding domain, an FcRn binding domain and one or more sugar chain receptor-binding domains) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo.
In the present invention, as a site at which an antigen is dissociated from an antigen-binding molecule, any site may be used as long as the site is within a cell and preferably, a site within early-stage endosome. In the present invention, the expression: “dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell” refers to dissociation of an antigen from an antigen-binding molecule as a result that the antigen (bound to an antigen-binding molecule outside a cell) is brought into contact with a cell expressing a sugar chain receptor (binding to the sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo. It is not necessary to dissociate all antigens taken up into a cell from antigen-binding molecules within the cell. It is sufficient if the rate of antigens from which antigen-binding molecules are dissociated (or antigen-binding molecules from which an antigen is dissociated) in the cell is high.
The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range, binds to the sugar chain receptor and then is taken up into the cell expressing a sugar chain receptor by endocytosis. In an acidic range, the antigen-binding molecule of the present invention is released from the sugar chain receptor, binds to FcRn (particularly human FcRn) in the acidic range and is recycled outside the cell. The antigen-binding molecule of the present invention (from which an antigen dissociates in the acidic range) recycled outside the cell, can bind again to an antigen. In this case, the antigen dissociated is decomposed in a lysosome within a cell. Therefore, every time the antigen-binding molecule of the present invention is recycled, the antigen present outside the cell expressing a sugar chain receptor (which bound to the antigen-binding molecule of the present invention) is decomposed in a lysosome within the cell (expressing a sugar chain receptor). As a result of the decomposition of the antigen, the number of antigens present outside a cell presumably decreases. Whether the number of antigens decreased or not can be evaluated by measuring the amount of antigen extracellularly present out of a body fluid such as blood, plasma, serum, urine, lymph fluid, saliva and tear when a cell expressing a sugar chain receptor is present within a living body, and evaluated by measuring the amount of antigen present in not only a body fluid taken out of a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear but also a culture fluid of the cell, if the cell (expressing a sugar chain receptor) is present outside a living body.
Dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from an antigen-binding molecule within the cell, can be promoted by the method (provided by the present invention) for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from an antigen-binding molecule within the cell, comprising bringing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo, more specifically by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body, or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used. Accordingly, whether or not the number of antigens present outside the cell decreased can be confirmed also by determining whether or not the amount of antigen present in plasma has decreased compared to the case where the antigen-binding molecule is not administered, or by determining whether or not the concentration of the antigen in plasma has been reduced by the ex-vivo method or administration of the antigen-binding molecule.
Whether the amount of antigen in plasma decreased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell, which is to be brought into contact with the antigen-binding molecule of the present invention expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
The present invention provides a method for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell, comprising bringing the antigen-binding molecule of the present invention containing an antigen-binding domain whose binding activity to the antigen changes depending upon the ion-concentration condition, into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule). The present invention further provides a method for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell, comprising bringing the antigen-binding molecule of the present invention containing an antigen-binding domain whose binding activity to the antigen has been changed depending upon the ion-concentration condition, into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule). The present invention further provides a method for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell, comprising, bringing the antigen-binding molecule containing an antigen-binding domain (in which at least one amino acid changing the binding activity of the antigen-binding domain to the antigen depending upon the calcium-ion concentration condition or pH condition) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule).
In the present invention, as the method for “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
The present invention provides a method for promoting uptake of an antigen-binding molecule or an antigen (binding to an antigen-binding molecule) into a cell expressing a sugar chain receptor, in-vivo or ex-vivo, comprising, in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor, increasing the number of binding domains to the sugar chain receptor.
In the present invention, “uptake . . . into a cell” refers to uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) into a cell by endocytosis. In the present invention, the expression “promoting uptake . . . into a cell” refers to increasing a speed of taking up an antigen-binding molecule, which binds to an antigen outside a cell, into the cell. Accordingly, in the present invention, whether uptake of an antigen-binding molecule or (an antigen binding to the antigen-binding molecule) was promoted or not is determined based on the uptake speed of the antigen-binding molecule or the antigen (binding to the antigen-binding molecule) into the cell has been increased or not. The uptake speed of an antigen into a cell can be calculated, for example, by adding an antigen-binding molecule and an antigen to a culture fluid containing a sugar chain receptor expression cell; and measuring a decrease in concentration of the antigen-binding molecule or the antigen (binding to the antigen-binding molecule) in the culture fluid with the passage of time, or measuring the amount of antigen-binding molecule or antigen (binding to the antigen-binding molecule) taken up into a sugar chain receptor expression cell with the passage of time.
In the present invention, as the method “for increasing the number of binding domains to the sugar chain receptor”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Uptake of the antigen-binding molecule of the present invention into a cell expressing a sugar chain receptor can be performed not only ex-vivo but also in vivo by administering the antigen-binding molecule. More specifically, in the present invention, whether or not uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) into a cell has been promoted can be confirmed by determining whether or not the clearance speed of an antigen present in plasma was promoted (whether or not the speed has been accelerated compared to the case where the antigen-binding molecule is not administered) or whether or not the antigen concentration in plasma is lowered by administration of the antigen-binding molecule, which is determined, for example, by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body, or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used.
Whether uptake is promoted or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell (which is brought into contact with the antigen-binding molecule of the present invention) expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is, for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
The present invention provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor) to the sugar chain receptor; at the same time, for promoting uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) containing an antigen-binding domain whose binding activity changes to an antigen depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains, which are contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor) to the sugar chain receptor; at the same time, for promoting uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) containing an antigen-binding domain whose binding activity to an antigen has been changed depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains, which are contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to the sugar chain receptor) to the sugar chain receptor; at the same time, for promoting uptake of an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) (in which at least one amino acid of the antigen-binding domain is an amino acid, which changes the binding activity of the antigen-binding domain to an antigen depending upon the calcium-ion concentration condition or pH condition).
In the present invention, as the method “for changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Method for Increasing the Number of Antigens to which a Single Antigen-Binding Molecule Binds
The present invention provides a method for increasing the number of antigens to which a single antigen-binding molecule binds, in vivo and ex-vivo, comprising increasing the number of binding domains to a sugar chain receptor in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and one or more binding domains to the sugar chain receptor.
In the present invention, the expression “the number of antigens to which a single antigen-binding molecule binds” refers to the number of antigens that an antigen-binding molecule can bind until it is decomposed and cleared. In the present invention, “increasing the number of antigens to which a single antigen-binding molecule can bind” refers to increasing the binding times of an antigen-binding molecule which repeats dissociation from an antigen molecule and association with another antigen molecule. The antigen molecule binding to an antigen-binding molecule may be the same antigen molecule or a different antigen molecule in a reaction system where both molecules are present. In other words, the binding times are the total binding times of an antigen-binding molecule to an antigen in the reaction system. To describe more specifically, provided that a process where an antigen-binding molecule bound to an antigen is taken up into a cell, dissociated from the antigen in endosome and returns outside the cell is regarded as one cycle, the number of cycle repeats until the antigen-binding molecule is decomposed and cleared is referred to the binding times. The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range binds to a sugar chain receptor and is then taken up into the cell expressing the sugar chain receptor by endocytosis. The antigen-binding molecule of the present invention is released from the sugar chain receptor in an acidic range and binds to FcRn (particularly human FcRn) in the acidic range and then returns outside the cell for recycle use. The antigen-binding molecule of the present invention, which is dissociated from an antigen in the acidic range and returns outside a cell for recycle use, can bind again to an antigen. Therefore, whether or not the number of cycles increased can be determined based on whether “uptake into a cell is promoted” or not, or whether “pharmacokinetics is improved” (described later) or not.
In the present invention, as the method “for increasing the number of binding domains to a sugar chain receptor”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Binding of the antigen-binding molecule of the present invention to an antigen can be performed also ex-vivo and whether or not the number of antigens binding to a single antigen-binding molecule was increased can be confirmed based on whether or not the clearance speed of an antigen present in plasma was promoted (whether or not the speed has been accelerated compared to the case where an antigen-binding molecule is not administered), which is determined by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body, or (2) a method of administering an antigen-binding molecule to a living body; or confirmed by determining whether or not the antigen concentration in plasma has been lowered by the ex-vivo method or by administering an antigen-binding molecule. As to the method (1), a method comprising taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body, can be also used.
Whether the number of antigens to which a single antigen-binding molecule binds has been increased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell, which is to be brought into contact with the antigen-binding molecule of the present invention, expresses a sugar chain receptor or not, can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
The present invention provides a method for increasing the number of binding domains, which are contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor) to the sugar chain receptor; at the same time, for increasing the number of antigens to which a single antigen-binding molecule (containing an antigen-binding domain whose binding activity to an antigen changes depending upon the ion-concentration condition) can bind, in-vivo or ex-vivo. The present invention further provides a method for increasing the number of binding domains, which are contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor) to the sugar chain receptor; at the same time, for increasing the number of antigens, to which a single antigen-binding molecule can bind, in-vivo or ex-vivo, comprising bringing an antigen-binding molecule (the number of antigens to which a single antigen-binding molecule can bind has been increased) containing an antigen-binding domain (whose binding activity to the antigen has been changed depending upon the ion-concentration condition) into contact with a cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain contained in the antigen-binding molecule). The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor of an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for increasing the number of antigens, to which a single antigen-binding molecule can bind (in which at least one amino acid of the antigen-binding domain is an amino acid, which changes the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition) in-vivo or ex-vivo.
In the present invention, as the method for “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
The present invention provides a method for enhancing an ability of an antigen-binding molecule to clear an antigen, in-vivo or ex-vivo, comprising increasing the number of binding domains to the sugar chain receptor in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to the sugar chain receptor.
The expression: the antigen present outside a cell, refers to an antigen present outside the cell expressing a sugar chain receptor. When the cell expressing a sugar chain receptor is present inside a living body, an antigen present outside the cells of a body fluid such as blood, plasma, serum, urine, lymph fluid, saliva and tear can be mentioned as an example (of the antigen present outside a cell). However, as long as the antigen-binding molecule (of the present invention administered to a living body) can bind to an antigen outside the cell expressing a sugar chain receptor, the antigen present outside a cell is not limited to the antigen present in these body fluids. Particularly preferable example of the antigen present outside a cell, an antigen present in plasma. When the cell expressing a sugar chain receptor is present outside a living body, not only a body fluid taken out from a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear, but also an antigen present in a culture fluid of the cell can be mentioned as an example of the antigen present outside a cell.
The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range, binds to the sugar chain receptor and then is taken up into the cell expressing the sugar chain receptor by endocytosis. In an acidic range, the antigen-binding molecule (of the present invention) is released from the sugar chain receptor, binds to FcRn (particularly human FcRn) in the acidic range. In this manner, the antigen-binding molecule of the present invention is returned again outside the cell for recycle use. The antigen-binding molecule of the present invention (from which an antigen dissociates in the acidic range) returned outside the cell for recycle use can bind again to an antigen. In this case, the antigen-binding molecule of the present invention dissociating from an antigen in the acidic range is recycled outside the cell can bind again to the antigen. In this case, the antigen dissociated is decomposed in a lysosome within a cell. Therefore, every time the antigen-binding molecule (of the present invention) is recycled, the antigen (which is present outside the cell expressing a sugar chain receptor and bound to the antigen-binding molecule) is decomposed in a lysosome within the cell (expressing a sugar chain receptor). As a result of such decomposition of the antigen, the number of antigens present outside the cell presumably decreases. Whether the number of antigens present outside a cell decreased or not can be evaluated by measuring the amount of antigen present outside a body fluid (such as blood, plasma, serum, urine, lymph fluid, saliva and tear) if a cell (expressing a sugar chain receptor) is present within a living body, and evaluated by measuring the amount of antigen present in not only a body fluid taken out of a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear but also a culture fluid of the cell, if the cell (expressing a sugar chain receptor) is present outside a living body.
In the present invention, as the method “for increasing the number of antigens-binding domains to a sugar chain receptor”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Whether or not an ability of an antigen-binding molecule to clear an antigen in-vivo or ex-vivo was enhanced by a method (provided by the present invention) comprising increasing the number of binding domains to the sugar chain receptor in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to the sugar chain receptor), can be confirmed by determining whether the antigen outside the cell was cleared or not by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body, or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method including taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used. Accordingly, whether or not the number of antigens present outside a cell decreased can be confirmed also by determining whether or not the amount of antigen present in plasma has been decreased compared to the case where the antigen-binding molecule is not administered or by determining whether or not the antigen concentration in plasma has been reduced by the ex-vivo method or administration of an antigen-binding molecule.
Whether the amount of antigen in plasma has decreased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell, which is to be brought into contact with the antigen-binding molecule of the present invention, expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
The present invention provides a method for increasing the number of binding domains (to a sugar chain receptor contained in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time for enhancing an ability of an antigen-binding molecule (which contains an antigen-binding domain whose binding ability to the antigen changes depending upon ion-concentration condition) to clear an antigen, in-vivo or ex-vivo. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor (contained in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for enhancing an ability of an antigen-binding molecule (which contains an antigen-binding domain whose binding ability to the antigen has been changed depending upon ion-concentration condition) to clear an antigen, in-vivo or ex-vivo. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor (contained in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for enhancing an ability of an antigen-binding molecule to clear an antigen, in-vivo or ex-vivo (in which at least one amino acid of the antigen-binding domain is an amino acid, which changes the binding activity of the antigen-binding domain to an antigen depending upon the calcium-ion concentration condition or pH condition).
In the present invention, as the method for “changing the binding activity of the antigen-binding domain to the antigen depending upon ion-concentration condition”, a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
The present invention provides a method of improving the pharmacokinetics of an antigen-binding molecule, comprising increasing the number of binding domains to a sugar chain receptor in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor.
In the present invention, “improvement of pharmacokinetics”, “enhancement of pharmacokinetics” or “excellent pharmacokinetics” can be rephrased by “improvement of retentivity in plasma (in blood)”, “enhancement of retentivity in plasma (in blood)”, “excellent retentivity in plasma (in blood)”, “extending retentivity in plasma (in blood)”. The meanings of these expressions are all the same.
In the present invention, the concept: “pharmacokinetics is improved” also includes extending the time period during which an antigen binds to an antigen-binding molecule after administration of the antigen-binding molecule. Whether the time period, during which antigen binds to an antigen-binding molecule after administration of the antigen-binding molecule, was extended or not can be determined by measuring concentration of an antigen-binding molecule-unbound antigen (not binding to an antigen-binding molecule) in plasma, more specifically, based on the time until the concentration of the antigen-binding molecule-unbound antigen in plasma increases, or the ratio of the concentration of the antigen-binding molecule-unbound antigen relative to total antigen concentration increases.
The concentration of the antigen-binding molecule-unbound antigen in plasma, or, the ratio of the concentration of an antigen-binding molecule-unbound antigen relative to total antigen concentration can be determined by a method known to those skilled in the art. For example, a measurement method employed in Pharm Res. (2006) 23 (1) 95-103. can be used. When an antigen plays some role in-vivo, whether or not the antigen has bound to an antigen-binding molecule (antagonist molecule) which neutralizes the function of the antigen can be evaluated by determining whether or not the function of the antigen has been neutralized. Whether or not the function of the antigen has been neutralized can be evaluated by measuring any one of in-vivo markers which reflects the function of the antigen. Whether or not an antigen has bound to an antigen-binding molecule (agonist molecule), which activates the function of the antigen, can be evaluated by measuring any one of in-vivo markers which reflects the function of the antigen.
Measurement, such as measurement of the concentration of an unbound antigen in plasma, measurement of the ratio of the amount of unbound antigen relative to the total antigen amount and measurement of in-vivo marker(s), is not particularly limited and preferably performed in a predetermined time after an antigen-binding molecule is administered. In the present invention, expression: a predetermined time after an antigen-binding molecule is administered, is not particularly limited and can be appropriately determined by those skilled in the art in consideration of the properties of the antigen-binding molecule to be administered. For example, one day, 3 days, 7 days, 14 days and 28 days after an antigen-binding molecule is administered are mentioned.
In the present invention, it is preferable that pharmacokinetics in a human is improved. If it is difficult to measure retentivity in plasma in a human, retentivity in plasma in a human can be estimated based on retentivity in plasma of a mouse (for example, normal mouse, human antigen expression transgenic mouse, human FcRn expressing transgenic mouse 32 lineage or 276 lineage (Jackson Laboratories) (Methods Mol Biol. (2010) 602, 93-104) etc., transgenic mouse, etc.) and a monkey (for example, crab-eating monkey).
The present invention provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for improving the pharmacokinetics of an antigen-binding molecule containing an antigen-binding domain, which changes the binding activity to an antigen depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for improving the pharmacokinetics of an antigen-binding molecule containing an antigen-binding domain, which has changed the binding activity to an antigen depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for improving the pharmacokinetics of an antigen-binding molecule containing an antigen-binding domain, whose at least one amino acid is an amino acid, which has changed the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition.
In the present invention, as a method for “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition” a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
Method for Promoting Dissociation of Antigen from Antigen-Binding Molecule
The present invention provides a method for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule, comprising increasing the number of binding domains to a sugar chain receptor in an antigen-binding molecule containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor.
In the present invention, as a site at which an antigen is dissociated from an antigen-binding molecule, any site may be used as long as the site is within a cell and preferably, a site within early-stage endosome. In the present invention, the expression: “dissociation of an antigen bound to an antigen-binding molecule outside a cell from the antigen-binding molecule within the cell” refers to dissociation of an antigen from an antigen-binding molecule as a result that the antigen (bound to an antigen-binding molecule outside a cell) is brought into contact with a cell expressing a sugar chain receptor (binding to the sugar chain receptor-binding domain contained in the antigen-binding molecule) in-vivo or ex-vivo. It is not necessary to dissociate all antigens taken up into a cell from an antigen-binding molecule within the cell. It is sufficient if the rate of antigens from which antigen-binding molecules are dissociated (or antigen-binding molecules from which an antigen is dissociated) in the cell is high.
The antigen-binding molecule of the present invention having a binding activity to a sugar chain receptor in a neutral pH range, binds to the sugar chain receptor and then is taken up into the cell expressing the sugar chain receptor by endocytosis. In an acidic range, the antigen-binding molecule of the present invention is released from the sugar chain receptor, binds to FcRn (particularly human FcRn) in the acidic range and is recycled outside the cell. The antigen-binding molecule of the present invention (from which an antigen dissociates in the acidic range) recycled outside the cell can bind again to an antigen. In this case, the antigen dissociated is decomposed in a lysosome within a cell. Therefore, every time the antigen-binding molecule of the present invention is recycled, the antigen present outside the cell expressing a sugar chain receptor (which bound to the antigen-binding molecule of the present invention) is decomposed in a lysosome within the cell (expressing a sugar chain receptor). As a result of the decomposition of the antigen, the number of antigens present outside a cell presumably decreases. Whether the number of antigens decreased or not can be evaluated by measuring the amount of antigen present outside cells of a body fluid such as blood, plasma, serum, urine, lymph fluid, saliva and tear when a cell expressing a sugar chain receptor is present within a living body; and evaluated by measuring the amount of antigen present in not only a body fluid taken out of a living body, such as blood, plasma, serum, urine, lymph fluid, saliva and tear but also a culture fluid of the cell, if the cell (expressing a sugar chain receptor) is present outside a living body.
Whether dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule has been promoted or not by a method of increasing the number of binding domains to a sugar chain receptor in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor) can be confirmed by determining whether the dissociation of an antigen (bound to an antigen-binding molecule outside the cell) from the antigen-binding molecule in the cell has been promoted or not, for example, by (1) a method (called an ex-vivo method), comprising taking out plasma containing an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with a cell expressing a sugar chain receptor for a predetermined period, taking the plasma outside the cell (called re-secretion or recycling) for recycle use, and returning the plasma containing a free antigen-binding molecule (not bound to the antigen) into the living body; or (2) a method of administering an antigen-binding molecule to a living body. As to the method (1), a method comprising taking out the plasma containing an antigen (binding to the antigen-binding molecule) once out of a living body, bringing the plasma into contact with an antigen-binding molecule and a cell expressing a sugar chain receptor for a predetermined time, and returning the plasma into the living body can be also used. Accordingly, whether or not the number of antigens present outside a cell decreased can be confirmed also by determining whether or not the amount of antigen present in plasma has decreased compared to the case where the antigen-binding molecule is not administered or by determining whether or not the concentration of the antigen in plasma has been reduced by the ex-vivo method or administration of an antigen-binding molecule.
Whether the amount of antigen in plasma decreased or not can be confirmed by determining whether or not the clearance speed of an antigen in the plasma (which is determined by the above (1) and (2) methods) has been promoted compared to the clearance speed of an antigen in the plasma, which is determined by the same method as in the above except that a human natural IgG (particularly human natural IgG1) is used in place of the antigen-binding molecule.
In the present invention, as the cell expressing a sugar chain receptor (binding to a sugar chain receptor-binding domain and contained in an antigen-binding molecule), any cell can be used as long as a desired sugar chain receptor is expressed in the cell. The cell is not limited to a specific cell. To specify the cell expressing a desired sugar chain receptor, database known in the art, such as Human Protein Atlas (http://www.proteinatlas.org/), can be used. Furthermore, whether the cell, which is to be brought into contact with the antigen-binding molecule of the present invention expresses a sugar chain receptor or not can be confirmed by a technique for determining expression of a gene encoding a desired sugar chain receptor and an immunological technique using an antibody binding to a desired sugar chain receptor. These techniques are known in the art. Since the cell expressing a sugar chain receptor can be brought into contact with an antigen-binding molecule and an antigen (binding to the antigen-binding molecule) not only outside a living body but also inside a living body, the expression: bringing the antigen-binding molecule into contact with the cell expressing a sugar chain receptor in the present invention, includes administering the antigen-binding molecule to a living body. The contact time is for example, one minute to several weeks, 30 minutes to one week, one hour to 3 days, and 2 hours to one day; in other words, the time required for an antigen-binding molecule or an antigen (binding to the antigen-binding molecule) to be taken up into a cell by endocytosis is appropriately employed.
For example, as the cell expressing an asialoglycoprotein receptor as a sugar chain receptor, a liver cell can be used. Furthermore, as the cell expressing a mannose receptor as a sugar chain receptor, a wide variety of cells including blood cells can be used.
The present invention provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell containing an antigen-binding domain, which changes the binding activity to an antigen depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule within the cell containing an antigen-binding domain, which has changed the binding activity to an antigen depending upon the ion-concentration condition. The present invention further provides a method for increasing the number of binding domains to a sugar chain receptor contained in an antigen-binding molecule (containing an antigen-binding domain, an FcRn binding domain and two or more binding domains to a sugar chain receptor); at the same time, for promoting dissociation of an antigen (bound to an antigen-binding molecule outside a cell) from the antigen-binding molecule (in which at least one amino acid of the antigen-binding domain is an amino acid, which changes the binding activity to an antigen depending upon the calcium-ion concentration condition or pH condition).
In the present invention, as a method for “changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition” a plurality of methods described as a method for producing an antigen-binding molecule in the specification may be appropriately used alone or in combination.
In the specification, an aspect expressed by “ . . . comprising” includes an aspect “essentially consisting of” and an aspect expressed by “ . . . consisting of”.
The contents of all patent literatures and reference documents explicitly cited in the specification are incorporated herein by reference.
The present invention will be described more specifically by way of Examples; however, the present invention is not limited to these Examples.
Improvement of clearance acceleration effect of antigen by pH-dependent antigen-binding antibody using a sugar chain receptor When an existing neutralizing antibody against a soluble antigen is administered, an antigen binds to the antibody, with the result that retentivity in plasma is presumably enhanced. Antibody generally has a long half-life period (1 week to 3 weeks); whereas, an antigen generally has a short half-life period (1 day or less). Because of this, the antigen bounds to an antibody in plasma acquires a significantly long half-life period compared to an antigen present alone. Consequently, if an existing neutralizing antibody is administered, the antigen concentration in plasma increases. Such a phenomenon has been reported in various documents dealt with neutralizing antibodies targeting a soluble antigen. Examples of the cases include IL-6 (J Immunotoxicol. 2005, 3, 131-9.), amyloid beta (mAbs, 2010, 2: 5, 1-13), MCP-1 (ARTHRITIS & RHEUMATISM 2006, 54, 2387-92), hepcidin (AAPS J. 2010, 4, 646-57.), sIL-6 receptor (Blood. 2008 Nov. 15; 112 (10): 3959-64.). It is reported that a total antigen concentration in plasma increases by approximately 10 fold to 1000 fold (the rate of increase varies depending upon the antigen) from a base line by administration of an existing neutralization activity. The term “total antigen concentration in plasma” used herein refers to the total concentration of antigens present in plasma, more specifically, a total of an antibody-binding antigen concentration and an antibody-unbound antigen concentration. In the case of such an antibody drug targeting a soluble antigen, an increase of the total antigen concentration in plasma is unfavorable. This is because in order to neutralize a soluble antigen, the antibody concentration in plasma at least higher than the total antigen concentration in plasma is required. More specifically, a 10-fold to 1000-fold increase of the total antigen concentration in plasma means that the antibody concentration in plasma (more specifically antibody dose) for neutralizing the antigen must be 10 fold to 1000 fold as high as that of the case where the total antigen concentration in plasma does not increase. In contrast, if the total antigen concentration in plasma can be reduced by 10 fold to 1000 fold compared to that of an existing neutralizing antibody, the dose of the antibody can be reduced by the same fold. As described above, an antibody capable of clearing soluble antigens from plasma, thereby reducing the total antigen concentration in plasma is extremely useful beyond an existing neutralizing antibody.
Regarding pH-Dependent Human IL-6 Receptor-Binding Antibody
H54/L28-IgG1, which is constituted of H54 (SEQ ID NO: 26) and L28 (SEQ ID NO: 27) (described in WO 2009/125825) is a humanized anti-IL-6 receptor antibody. GL1-IgG1 (Fv4-IgG1 described in WO 2009/125825), which is constituted of VH3-IgG1 (SEQ ID NO: 28) and VL3-CK (SEQ ID NO: 29), is a humanized anti-IL-6 receptor antibody prepared by adding a property of binding to a soluble human IL-6 receptor in a pH-dependent manner (binds at pH 7.4 and dissociates at pH 5.8) compared to H54/L28-IgG1. In an in-vivo test using mice (described in WO 2009/125825), it was demonstrated that clearance of a soluble human IL-6 receptor can be significantly accelerated in a group in which a mixture of GL1-IgG1 and a soluble human IL-6 receptor (as an antigen) was administered, compared to a group in which a mixture of H54/L28-IgG1 and a soluble human IL-6 receptor (as an antigen) was administered.
A soluble human IL-6 receptor bound to an antibody (which is capable of binding to a conventional soluble human IL-6 receptor) is recycled together with the antibody into plasma by means of FcRn. In contrast, the antibody binding to a soluble human IL-6 receptor in a pH-dependent manner dissociates the soluble human IL-6 receptor bound to the antibody under the acidic condition within endosome. The soluble human IL-6 receptor dissociated is decomposed by lysosome. Thus, clearance of the soluble human IL-6 receptor can be significantly accelerated. Furthermore, the antibody binding to the soluble human IL-6 receptor in a pH-dependent manner is recycled by FcRn into plasma. The antibody recycled can bind to a soluble human IL-6 receptor again. By repeating this process, a single antibody molecule can repeatedly bind to a soluble human IL-6 receptor (
An IgG antibody acquires long retentivity in plasma by binding to an FcRn. Binding of IgG to FcRn is observed only under an acidic condition (pH 6.0) and rarely observed under a neutral condition (pH 7.4). An IgG antibody is nonspecifically taken up into a cell, binds to FcRn under an acidic condition within an endosome, returns to the cell surface and dissociated from FcRn under a neutral condition of plasma. If a mutation is introduced into the Fc region of IgG to abolish binding to FcRn under an acidic condition, IgG cannot be recycled from the endosome to plasma, with the result that retentivity of the antibody in plasma is significantly reduced. A method for improving the retentivity of an IgG antibody in plasma, a method of improving binding to FcRn under an acidic condition has been reported. By improving binding to FcRn under an acidic condition by introducing an amino acid substation into the Fc region of an IgG antibody, a recycle rate from an endosome to plasma increases, with the result that the retentivity in plasma increases.
Improvement of Antigen Clearance Acceleration Effect by pH-Dependent Antigen-Binding Antibody Using a Sugar Chain Receptor
An antibody binding to an antigen in a pH-dependent manner is extremely useful since it can accelerate clearance of soluble antigens and lower a total antigen concentration in plasma and a single antibody molecule has an effect of repeatedly binding to a soluble antigen multiple times. The antigen clearance acceleration effect is further improved by a method comprising adding a sugar chain to an antibody capable of binding to an antigen in a pH-dependent manner (the sugar chain added to the antibody associates with a sugar chain receptor only observed under a neutral condition (pH 7.4) and dissociates under an acidic condition (pH 6.0)); allowing the antibody to bind to a soluble antigen and to take up into a cell depending upon the sugar-chain receptor, dissociating the antibody from the sugar-chain receptor in an endosome, at the same time, from the soluble antigen, binding the antibody to FcRn, and recycling the antibody into plasma again. This method was evaluated (
For the above method to effectively work, it is considered necessary that the sugar chain binds to the sugar chain receptor and the antigen binds to the antibody in a pH-dependent manner; that the antigen-binding molecule binds to the sugar chain receptor as well as the antigen under a neutral condition, with the result that an antibody-antigen complex is taken up into a cell via the sugar chain receptor; and that the antigen-binding molecule needs to dissociate from the sugar chain receptor as well as the antigen under an acidic condition of an endosome.
As the antigen and antibody having such a feature, an antibody against an IL-6 receptor, Fv4-IgG1 (described in WO 2009/125825) is known. This is referred to as GL1-IgG1 in the present invention.
Furthermore, as the sugar chain and sugar chain receptor having such a feature, galactose and an asialoglycoprotein receptor, and mannose and a mannose receptor are conceivable. It is known that the asialoglycoprotein receptor (a sugar chain receptor), which interacts with galactose in a pH-dependent manner, has high binding activity in the neutral pH range but low binding activity in an acidic pH range (J. Biol. Chem. (1989) 274 (50), 35400-35406). Similarly, it is known that the mannose receptor (a sugar chain receptor), which interacts with mannose in a pH-dependent manner, has high binding activity in a neutral pH range but low binding activity in an acidic pH range (J. Biol. Chem. (1994) 269 (45), 28405-28413).
Preparation of pH-Dependent Human IL-6 Receptor Binding Antibody Having an N-Linked Glycosylation Sequence
To GL1-IgG1 consisting of VH3-IgG1 (SEQ ID NO: 28) and VL3-CK (SEQ ID NO: 29), a mutation was introduced so as to contain an N-linked glycosylation sequence Asn-X-Ser/Thr, where X represents an amino acid except Pro, Ser/Thr means Ser or Thr. More specifically, VH3-M111 (SEQ ID NO: 31) having a heavy-chain constant region M111 (SEQ ID NO: 30) was prepared by substituting the 297th (EU numbering) Asn of an IgG1 heavy-chain constant region with Ala; and H01-M111 (SEQ ID NO: 32) was prepared by substituting the 75th (Kabat numbering) Lys of a VH3-M111 heavy-chain variable region with Asn. Furthermore, L02-CK (SEQ ID NO: 33) was prepared by substituting the 18th (kabat numbering) Ser of a VL3-CK light-chain variable region with Asn; L03-CK (SEQ ID NO: 34) was prepared by substituting 20th Thr with Asn; L04-CK (SEQ ID NO: 35) was prepared by substituting 24th Gln with Asn; and L06-CK (SEQ ID NO: 36) was prepared by substituting 20th Thr and 24th Gln each with Asn. An amino acid substituent was introduced by a method known in the art and described in Reference Example 1
H54/L28-IgG1 consisting of H54 (SEQ ID NO: 26) and L28 (SEQ ID NO: 27); GL1-IgG1 consisting of VH3-IgG1 (SEQ ID NO: 28) and VL3-CK (SEQ ID NO: 29); GL1-M111 consisting of VH3-M111 (SEQ ID NO: 31) and VL3-CK; GL2-M111 consisting of VH3-M111 and L02-CK (SEQ ID NO: 33); GL3-M111 consisting of VH3-M111 and L03-CK (SEQ ID NO: 34), GL4-M111 consisting of VH3-M111 and L04-CK (SEQ ID NO: 35), GL5-M111 consisting of VH3-M111 and L06-CK (SEQ ID NO: 36); GL6-M111 consisting of H01-M111 (SEQ ID NO: 32) and VL3-CK; GL7-M111 consisting of H01-M111 and L02-CK; GL8-M111 consisting of H01-M111 and L03-CK; GL9-M111 consisting of H01-M111 and L04-CK; GL10-M111 consisting of H01-M111 and L06-CK; and GL5-IgG1 consisting of VH3-IgG1 and L06-CK were expressed and purified in accordance with methods known to those skilled in the art described in Reference Example 2.
In human natural IgG1, an N-linked sugar chain is added to the 297th Asn residue (EU numbering). In this Example, to easily evaluate introduction of an N-linked sugar chain into a variable region, a modified constant region named M111, which was prepared by substituting the 297th Asn with Ala, was used.
Glycosylation of an antibody, to which an N-linked glycosylation sequence was introduced, was evaluated by reducing SDS-PAGE. To each of GL1-M111 to GL10-M111 (6 μg aliquots), Tris-Glycine SDS Sample Buffer (2×) (TEFCO) containing a 5% 2-mercaptoethanol (Wako) was added. Thereafter, the mixture was incubated at 70° C. for 5 minutes, a sample to be subjected to electrophoresis was prepared. After electrophoresis was performed by a 12% SDS-PAGE mini 15 well (TEFCO) with Precision plus blue standard (Bio-Rad) used as a molecular-weight marker and CBB staining was performed by CBB Stain One (Nacalai tesque). The obtained electrophoretic pattern is shown in
In GL1-M111 in which a sugar chain is added to neither a heavy chain nor a light chain, a heavy chain emerged at the lower end of the 50 kDa molecular-weight marker, a light chain emerged at the upper end of the 25 kDa molecular-weight marker. In GL2-M111 to GL4-M111 in which a single glycosylation site was introduced in a light chain, a band corresponding to the light chain shifted toward high molecular weight side compared to GL1-M111. In GL5-M111 in which two glycosylation sites were introduced in a light chain, a band corresponding to the light chain shifted toward further higher molecular weight side compared to GL2-M111 to GL4-M111. In GL6-M111 in which a single glycosylation site was introduced in a heavy chain, a band corresponding to a heavy chain shifted toward a high molecular weight side compared to GL1-M111.
In GL7-M111 to GL9-M111 prepared by introducing two glycosylation sites in total in a single site of a heavy chain and a sites of a light chain, respectively, band shift of the heavy chain and light chain toward a high molecular weight side was observed compared to GL1-M111. GL10-M111 prepared by introducing three glycosylation sites in total in a single site of a heavy chain and two sites of a light chain, a band shift of a heavy chain towards a high molecular weight side than GL1-M111 and a band shift of the light chain towards a high molecular weight side than GL7-M111 to GL9-M111 were observed.
From these results, it was demonstrated that a plurality of glycosylation sites can be simultaneously introduced to both heavy chain and light chain.
Before and after removal of sialic acid by neuraminidase, anion exchange chromatography was performed. Based on a shape change between the chromatograms, whether or not the N-linked sugar chain that bound to is a high-mannose sugar chain and whether or not sialic acid binds to a terminal of a complex sugar chain were evaluated. To samples of GL1 to GL10 prepared with a 50 mmol/L Acetate pH 5.0, neuraminidase (Roche) was added. The mixture was allowed to stand still at 37° C. overnight and subjected to anion exchange chromatography performed by TSK-gel DEAE-NPR (Tosoh) in accordance with a two-liquid gradient method using 10 mmol/L Tris-HCl, pH 7.5 as mobile phase A and 10 mmo/L Tris-HCl/150 mmol/L NaCl, pH 7.5 as mobile phase B. Chromatograms are shown in
GL1-M111 (no sugar chain was added) showed a single peak before the neuraminidase treatment and no change was observed in the chromatogram after the neuraminidase treatment. In contrast, GL2-M111 to GL10-M111 (a sugar chain was added), heterogeneous peaks were observed before the neuraminidase treatment but the number of detection peaks decreased after the neuraminidase treatment. This means that sialic acid was added to a sugar chain terminal of each of GL2-M111 to GL10-M111, more specifically means that N-linked sugar chain added to GL2-M111 to GL10-M111 is not high-mannose sugar chain but a complex sugar chain having a plurality of sialic acids bound thereto. From this, it was confirmed that a complex sugar chain molecule with galactose exposed at a terminal can be prepared by a neuraminidase treatment.
To estimate that the N-linked sugar chain was added to GL5-M111 based on mass, mass analysis was performed. After a neuraminidase treatment, GL5-M11 was subjected to a reducing treatment with DTT (Wako) and then subjected to RP-LC/ESI-MS by use of Ultimate3000 (Dionex) and LTQ VELOS (Thermo scientific). Which one of bibranched N-linked sugar chains shown in Table 1 was added was estimated based on the mass and the obtained mass chromatograms are shown in
With an increase of the number of galactose exposed at an N-linked sugar chain terminal, a recognition efficiency via a sugar chain receptor conceivably increases. Then, addition of G2, G3 and G4 among the bibranched N-linked sugar chains was observed. As shown in
Neuraminidase, which was used for removing sialic acid from the N-linked sugar chain terminal and still contained in GL5-M111, was inactivated. After the neuraminidase treatment, GL5-M111 (GL5-M111-SA (−)) was purified with Protein A and incubated at 60° C. for 10 minutes (heat treated sample).
To GL5-M111-SA (−) (SA (−) means that sialic acid is removed) and a heat treated sample, to which GL5-M111 (GL5-M111-SA (+)) (SA (+) means that sialic acid remains without removing) (not treated with neuraminidase) was added, were allowed to stand still at 37° C. for 6 hours. These samples were analyzed by the same anion exchange chromatography method used for observation of an N-linked sugar chain. The obtained chromatograms are shown in
As shown in
Preparation of Sample by Replacing Constant Region with IgG1
It was shown that a bibranched N-linked sugar chain can be added to a light-chain variable region due to a modification introduced in GL5. Then, GL1-IgG1 and GL5-IgG1 were prepared by replacing a constant region from M111 to IgG1.
GL1-IgG1 and GL5-IgG1 were analyzed by reducing SDS-PAGE in the same manner as in the sample having M111 used in combination. The obtained electrophoretic patterns are shown in
As shown in
Evaluation of Binding to Human IL-6 Receptor (hIL6R)
GL1-IgG1-SA, GL1-M111-SA, GL2-M111-SA, GL3-M111-SA, GL4-M111-SA, GL5-M111-SA, GL6-M111-SA, GL7-M111-SA, GL8-M111-SA, GL9-M111-SA and GL10-M111-SA were prepared and treated with neuraminidase in accordance with the method mentioned above to remove a terminal sialic acid. In this manner, GL1-IgG1-SA (−), GL1-M111-SA (−), GL2-M111-SA (−), GL3-M111-SA (−), GL4-M111-SA (−), GL5-M111-SA (−), GL6-M111-SA (−), GL7-M111-SA (−), GL8-M111-SA (−), GL9-M111-SA (−) and GL10-M111-SA (−) having galactose exposed at a terminal, were prepared.
Kinetic analysis on the antigen-antibody reaction between each of GL1-IgG1-SA (−), GL1-M111-SA (−), GL2-M111-SA (−), GL3-M111-SA (−), GL4-M111-SA (−), GL5-M111-SA (−), GL6-M111-SA (−), GL7-M111-SA (−), GL8-M111-SA (−), GL9-M111-SA (−), GL10-M111-SA (−) and a human IL-6 receptor was performed by use of Biacore T100 (GE Healthcare). An appropriate amount of protein A (Invitrogen) was immobilized onto Sensor chip CM5 (GE Healthcare) by the amine coupling method and then a target antibody was allowed to capture. Subsequently, a human IL-6 receptor dilution solution and a running buffer (a blank) were injected at a flow rate of 20 μL/min for 3 minutes to allow the human IL-6 receptor to interact with the antibody captured on the sensor chip. Either one of two types of running buffers pH 7.4 and pH 6.0 containing 10 mmol/L ACES, 150 mmol/L NaCl, and 0.05% (w/v) Tween20 was used and each buffer was employed for dilution of IL-6R. Thereafter, the running buffer was fed at a flow rate of 20 μL/min for 5 minutes. After observation of dissociation of the IL-6 receptor, 10 mmol/L Glycine-HCl (pH 1.5) was injected at a flow rate of 30 μL/min for 30 seconds to regenerate the sensor chip. All samples were measured at 37° C. From the sensorgram obtained by measurement, an association constant, ka (1/Ms) and a dissociation constant, kd (1/s) as kinetics parameters were computationally obtained. Based on the obtained values, KD (M) of each antibody to a human IL-6 receptor was calculated. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare). The resultant KD values of individual antibodies determined at pH 7.4 and pH 6.0 are shown in Table 2 below. It was found that significant difference was not observed in KD value between individual antibodies at each of the two conditions: pH 7.4 and pH 6.0, compared to GL1-IgG1-SA (−).
From these results, GL5-M111, to which an N-linked glycosylation site is introduced at the 18th and 24th positions (Kabat numbering) of a light chain, was selected as a modified antibody, which has a complex sugar chain having a galactose at a terminal effectively introduced therein and retains a binding activity to a human IL-6 receptor and pH dependency.
Then, kinetic analysis of an antigen-antibody reaction between each of GL1-M111-SA (−) and GL5-M111-SA (−) and a human IL-6 receptor was performed by using Biacore T100 (GE Healthcare). In both cases, measurement was performed by using an antibody treated with sialidase as a sample. An appropriate amount of Anti-Human IgG (γ-chain specific) F(ab′)2 fragment antibody produced in goat (Sigma) was immobilized onto Sensor chip CM5 (GE Healthcare) in accordance with the amine coupling method and then a target antibody was allowed to capture. Subsequently, a human IL-6 receptor dilution solution and a running buffer (a blank) were injected at a flow rate of 20 μL/min for 3 minutes to allow the human IL-6 receptor to interact with the antibody captured on the sensor chip. Either one of two types of running buffers pH 7.4 and pH 6.0 containing 10 mmol/L ACES, 150 mmol/L NaCl, and 0.05% (w/v) Tween20 was used, and each buffer was employed for dilution of IL-6R. Thereafter, a running buffer was fed at a flow rate 20 μL/min for 5 minutes. After dissociation of the IL-6 receptor was observed, 10 mmol/L Glycine-HCl (pH 1.5) was injected at a flow rate 30 μL/min for 5 seconds. This procedure was repeated five times to regenerate a sensor chip. All samples were measured at 37° C. From the sensorgram obtained by measurement, an association constant, ka (1/Ms) and a dissociation constant kd (1/s) as kinetics parameters were computationally obtained. From the values, KD (M) of each antibody to a human IL-6 receptor was calculated. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare). The resultant KD values of individual antibodies determined at each of pH 7.4 and pH 6.0 are shown in Table 3 below. No significant difference was observed in KD value between the two antibodies at each of the two conditions: pH 7.4 and pH 6.0.
Next, kinetic analysis of antigen-antibody reactions between each of GL1-IgG1-SA (+), H54L28-IgG1-SA (+), GL1-IgG1-SA (−) and GL5-IgG1-SA (−) and a human IL-6 receptor was performed by using Biacore T100 (GE Healthcare). GL1-IgG1-SA (−) and GL5-IgG1-SA (−) were treated with sialidase and then used as measurement samples. An appropriate amount of Anti-Human IgG (γ-chain specific), F(ab′)2 fragment antibody produced in goat (Sigma) was immobilized onto Sensor chip CM5 (GE Healthcare) in accordance with the amine coupling method and then a target antibody was allowed to capture. Subsequently, a human IL-6 receptor dilution solution and a running buffer (a blank) were injected at a flow rate of 20 μL/min for 3 minutes to allow the human IL-6 receptor to interact with the antibody captured on the sensor chip. Either one of two types of running buffers pH 7.4 and pH 6.0 containing 10 mmol/L ACES, 150 mmol/L NaCl, and 0.05% (w/v) Tween20 was used and each buffer was employed for dilution of IL-6R. Thereafter, a running buffer was fed at a flow rate 20 μL/min for 5 minutes. After dissociation of the IL-6 receptor was observed, 10 mmol/L Glycine-HCl (pH 1.5) was injected at a flow rate of 30 μL/min for 5 seconds. This procedure was repeated five times to regenerate the sensor chip. All samples were measured at 37° C. From the sensorgram obtained by measurement, an association constant, ka (1/Ms) and a dissociation constant kd (1/s) as kinetics parameters were computationally obtained. From the values, KD (M) of each antibody to a human IL-6 receptor was calculated. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare). The KD values of individual antibodies determined at each of the two conditions: pH 7.4 and pH 6.0 are shown in Table 4 below.
To a normal mouse (C57BL/6J mouse, Charles River Japan), hsIL-6R (soluble human IL-6 receptor prepared in Reference Example 3) was solely administered or hsIL-6R and anti-human IL-6 receptor antibody were simultaneously administered. Thereafter, in-vivo kinetics of the hsIL-6R and the anti-human IL-6 receptor antibody were evaluated. A hsIL-6R solution (5 μg/mL) or a mixture solution of the hsIL-6R and the anti-human IL-6 receptor antibody (5 μg/mL and 0.1 mg/mL respectively) was administered once to caudal vein in a dose of 10 mL/kg. At this time, since anti-human IL-6 receptor antibody is excessively present compared to hsIL-6R, it is considered that almost all hsIL-6R molecules bind to the antibody. Blood was sampled 15 minutes, 7 hours, 1 day, 2 days, 3 days, 4 days, 7 days, 14 days, 21 days and 28 days after the administration. The blood sampled was immediately centrifuged at 4° C., 15,000 rpm for 15 minutes to obtain plasma. The plasma separated was stored in a freezer set at −20° C. or less until measurement. As the anti-human IL-6 receptor antibody, GL1-M111, GL5-M111, H54/L28-IgG1, GL1-IgG1 and GL5-IgG1 mentioned above were used.
The concentration of an anti-human IL-6 receptor antibody in mouse plasma was measured by ELISA. First, Anti-Human IgG (γ-chain specific) F(ab′)2 Fragment of Antibody (SIGMA) was dispensed in Nunc-Immuno Plates, MaxiSoup (Nalge nunc International). The plates were allowed to stand still at 4° C. overnight to prepare Anti-Human IgG immobilized plates. Samples having a plasma concentration of 0.8, 0.4, 0.2, 0.1, 0.05, 0.025 and 0.0125 μg/mL were prepared for forming a calibration curve sample and a mouse plasma measurement sample diluted 100 fold or more were prepared. To each (100 μL) of the calibration-curve samples and the plasma measurement sample, 20 ng/mL hsIL-6R (200 μL) was added. The mixture was allowed to stand still at room temperature for one hour, and thereafter dispensed to the Anti-Human IgG immobilized plates and allowed to stand still at room temperature further for one hour. Thereafter, Biotinylated Anti-human IL-6R Antibody (R&D) was reacted at room temperature for one hour, and then, Streptavidin-PolyHRP80 (Stereospecific Detection Technologies) was reached at room temperature for one hour. Then, a chromogenic reaction was performed using TMB One Component HRP Microwell Substrate (BioFX Laboratories) as a substrate and terminated with 1N-Sulfuric acid (Showa Chemical). Thereafter, the absorbance (of the plates) was measured by a micro plate reader at 450 nm. The concentration in the mouse plasma was computationally obtained from the absorbance shown in the calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). A change of the antibody concentration in normal mouse plasma with time after intravenous administration, measured by this method, is shown in
Measurement of hsIL-6R Concentration in Plasma by Electrochemiluminescence Assay
Concentration of hsIL-6R in mouse plasma was measured by electrochemiluminescence assay. Samples having a plasma hsIL-6R concentration of 2000, 1000, 500, 250, 125, 62.5 and 31.25 pg/mL were prepared for forming a calibration curve sample and a mouse plasma measurement sample diluted to 50 fold or more were prepared. Monoclonal Anti-human IL-6R Antibody (R&D) labeled with ruthenium by means of SULFO-TAG NHS Ester (Meso Scale Discovery), Biotinylated Anti-human IL-6R Antibody (R&D), and a WT-IgG1 solution were mixed and reacted at 37° C. overnight. At this time, the final concentration of WT-IgG1 (an anti-human IL-6 receptor antibody) constituted of H (WT) (SEQ ID NO: 37) and L (WT) (SEQ ID NO: 38) was set at 333 μg/mL, which is as excessively high as the concentration of anti-human IL-6 receptor antibody contained in a sample, in order that almost all hsIL-6R molecules in the sample bind to WT-IgG1. Thereafter, the reaction mixture was dispensed to MA400 PR Streptavidin Plates (Meso Scale Discovery). After the reaction was further performed at room temperature for one hour and washed, Read Buffer T(x4)(Meso Scale Discovery) was dispensed. Immediately after that, measurement was performed by SECTOR PR 400 reader (Meso Scale Discovery). The concentration of hSIL-6R was computationally obtained based on the value shown in a calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). A change of hsIL-6R concentration with time in plasma of a normal mouse after intravenous injection, measured by this method, is shown in
Binding Effect of pH-Dependent Human IL-6 Receptor
The in-vivo test results of H54/L28-IgG1 and GL1-IgG1 (to which a pH-dependent human IL-6 receptor bound) were compared. As shown in
The in-vivo test results of GL1-M111 or GL1-IgG1 and GL5-M111 or GL5-IgG1 (having an N-linked sugar chain added) were compared. As shown in
When a conventional neutralization antibody (such as H54/L28-IgG1-SA (+)) is administered, clearance of an antigen binding to the antibody decreases, and the antigen remains for a longer time in plasma. It is unfavorable that plasma retentivity of the antigen that is desired to be neutralized is prolonged by administration of an antibody. The plasma retentivity of an antigen can be shortened by adding pH-dependent antigen-binding property (associate under a neutral condition and dissociates under an acidic condition) to an antibody. This time, the plasma retentivity of an antigen can be further shortened by addition of an N-linked sugar chain. Furthermore, it was shown that by administering an antibody capable of binding to an antigen in a pH-dependent manner (capable of binding to FcRn under a neutral condition (pH 7.4)), the same clearance as the clearance of an antigen alone can be attained. Up to now, a method attaining the same clearance as clearance of an antigen alone by administering an antibody has not been known. The method found in the investigation is extremely useful as a method for suppressing retentivity of an antigen (which is desired to be neutralized) from extending, by administration of an antibody. Furthermore, in the investigation, an advantage, i.e., acceleration of clearance of an antigen, was found for the first time by addition of an N-linked sugar chain (which is not involved in binding to an antigen) to an antibody in combination with use of an antibody binding to an antigen in a pH-dependent manner. Moreover, the site of the residues, to which an N-linked sugar chain (not involved in binding to an antigen) is added, are not limited to 20th and 24th residues (kabat numbering) of a light-chain variable region of GL5-M111 or GL5-IgG1. From this, it is considered that clearance of an antigen can be effectively accelerated by an antibody having an N-linked sugar chain added thereto, as long as the addition site is not relevant to amino acid substitution, not involved in binding to an antigen and the N-linked sugar chain can be added to the site.
Preparation of Human IL-6 Receptor pH-Dependent Binding Antibody Having High Mannose Sugar Chain
GL1-IgG1, which is constituted of VH3-IgG1 (SEQ ID NO: 28) and VL3-CK (SEQ ID NO: 29), and GL5-IgG1, which is constituted of VH3-IgG1 (SEQ ID NO: 28) and L06-CK (SEQ ID NO: 36) were expressed and purified in accordance with the methods (known to those skilled in the art) described in Reference Example 2. In temporarily introducing an expression vector, kifnensien (SIGMA) was added to a cell culture solution so as to obtain a concentration of 10 μg/mL. In this manner, GL1-IgG1_kif+ and GL5-IgG1_kif+ having a high mannose sugar chain were prepared.
Glycosylation of an antibody having an N-linked glycosylation sequence introduced therein was observed by reducing SDS-PAGE. To each of GL1-G1_kif+ (5 μg aliquots) and GL5-G1_kif+ (5 μg), Tris-Glycine SDS Sample Buffer (2×) (TEFCO) containing a 5% 2-mercaptoethanol (Wako) was added. Then, the mixtures were incubated at 70° C. for 5 minutes to prepare samples for electrophoresis. Electrophoresis was performed using a 12% SDS-PAGE mini 15 well (TEFCO) and with Precision plus blue standard (Bio-Rad) as a molecular-weight marker, and thereafter, CBB staining was performed with CBB Stain One (Nacalai tesque). The obtained electrophoretic patterns are shown in
As shown in the Figure, the light chain of GL5-IgG1_kif+ made a large shift toward a high molecular weight side compared to the light chain of GL1-IgG1_kif+. From this, it is considered that N-linked sugar chain binds to two sites of the light chain even in the presence of kifnensien.
To estimate an N-linked sugar chain added to GL5-G1_kif+ from mass, mass analysis was performed. GL5-M11 was treated with neuraminidase and reduced by a treatment with DTT (Wako), and RP-LC/ESI-MS was performed by use of Ultimate3000 (Dionex) and LTQ VELOS (Thermo scientific). Which of the high mannose N-linked sugar chains shown in Table 5 was added was estimated from mass. The obtained mass chromatogram is shown in
Evaluation of Binding to Human IL-6 Receptor (hIL6R)
Using Biacore T100 (GE Healthcare), kinetic analysis of antigen-antibody reactions between each of GL1-IgG1_kif+ and GL5-IgG1_kif+ and a human IL-6 receptor was performed. An appropriate amount of Anti-Human IgG (γ-chain specific) F(ab′)2 fragment antibody produced in goat (Sigma) was immobilized onto Sensor chip CM5 (GE Healthcare) by the amine coupling method and then a target antibody was allowed to capture. Subsequently, a human IL-6 receptor dilution solution and a running buffer (a blank) were injected at a flow rate of 20 μL/min for 3 minutes to allow the human IL-6 receptor to interact with the antibody captured on the sensor chip. Either one of two types of running buffers (pH 7.4 and pH 6.0 containing 10 mmol/L ACES, 150 mmol/L NaCl, and 0.05% (w/v) Tween20) was used, and each buffer was employed for dilution of IL-6R. Thereafter, a running buffer was fed at a flow rate 20 μL/min for 5 minutes. After dissociation of the IL-6 receptor was observed, a 10 mmol/L Glycine-HCl (pH 1.5) solution was injected at a flow rate of 30 μL/min for 5 seconds. This procedure was repeated five times to regenerate the sensor chip. All samples were measured at 37° C. From the sensorgram obtained by measurement, an association constant, ka (1/Ms) and a dissociation constant kd (1/s) as kinetics parameters were computationally obtained. From the values, KD (M) of each antibody to a human IL-6 receptor was calculated. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare). The resultant KD values of individual antibodies determined at pH 7.4 or pH 6.0 are shown in Table 6 below. A significant difference between KD values of both antibodies was not observed.
To a normal mouse (C57BL/6J mouse, Charles River Japan), hsIL-6R (soluble human IL-6 receptor prepared in Reference Example 3) was solely administered or hsIL-6R and an anti-human IL-6 receptor antibody were simultaneously administered. Thereafter, in-vivo kinetics of the hsIL-6R and the anti-human IL-6 receptor antibody were evaluated. A hsIL-6R solution (5 μg/mL) or a mixture solution of the hsIL-6R and the anti-human IL-6 receptor antibody (5 μg/mL and 0.1 mg/mL respectively) was administered once to caudal vein in a dose of 10 mL/kg. At this time, since anti-human IL-6 receptor antibody is excessively present compared to hsIL-6R, it is considered that almost all hsIL-6R molecules bind to the antibody. After the administration, blood was sampled in 15 minutes, 7 hours, on 1 day, 2 days, 3 days, 4 days and 7 days. The blood sampled was immediately centrifuged at 4° C., 15,000 rpm for 15 minutes to obtain plasma. The plasma separated was stored in a freezer set at −20° C. or less until measurement. As anti-human IL-6 receptor antibody, GL1-IgG1_kif+ and GL5-IgG1_kif+ mentioned above were used.
The concentration of an anti-human IL-6 receptor antibody in mouse plasma was measured by ELISA. First, Anti-Human IgG (γ-chain specific) F(ab′)2 Fragment of Antibody (SIGMA) was dispensed in Nunc-Immuno Plates, MaxiSoup (Nalge nunc International). The mixture was allowed to stand still at 4° C. overnight to prepare an Anti-Human IgG immobilized plates. Samples having a plasma concentration of 0.8, 0.4, 0.2, 0.1, 0.05, 0.025 and 0.0125 μg/mL were prepared for forming a calibration curve sample and a mouse plasma measurement sample diluted 100 fold or more were prepared. To each (100 μL) of the calibration-curve samples and plasma measurement sample, 20 ng/mL hsIL-6R (200 μL) was added. The mixture was allowed to stand still at room temperature for one hour. Thereafter, the mixture was dispensed to the Anti-Human IgG immobilized plates and then allowed to stand still at room temperature for one hour. Thereafter, Biotinylated Anti-human IL-6R Antibody (R&D) was reacted at room temperature for one hour, and then, Streptavidin-PolyHRP80 (Stereospecific Detection Technologies) was reacted at room temperature for one hour. Then, a chromogenic reaction was performed using TMB One Component HRP Microwell Substrate (BioFX Laboratories) as a substrate and terminated with 1N-Sulfuric acid (Showa Chemical). Thereafter, the absorbance was measured by a micro plate reader at 450 nm. The concentration in the mouse plasma was computationally obtained from the absorbance shown in the calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). A change of the antibody concentration with time in normal mouse plasma after intravenous administration, measured by this method, is shown in
Measurement of hsIL-6R Concentration in Plasma by Electrochemiluminescence Assay
Concentration of hsIL-6R in plasma in a mouse was measured by electrochemiluminescence assay. Samples of hsIL-6R having a concentration of 2000, 1000, 500, 250, 125, 62.5 and 31.25 pg/mL were prepared for forming a calibration curve sample and a mouse plasma measurement sample diluted to 50 fold or more were prepared. A Monoclonal Anti-human IL-6R Antibody (R&D) labeled with ruthenium by means of SULFO-TAG NHS Ester (Meso Scale Discovery), Biotinylated Anti-human IL-6R Antibody (R&D) and a WT-IgG1 solution were mixed and reacted at 37° C. overnight. At this time, the final concentration of WT-IgG1 (constituted of H (WT) (SEQ ID NO: 37) and L (WT) (SEQ ID NO: 38) serving as an anti-human IL-6 receptor antibody) was set at 333 μg/mL, which was as excessively high as the concentration of anti-human IL-6 receptor antibody contained in a sample in order that almost all hsIL-6R molecules in the sample bind to WT-IgG1. Thereafter, the reaction mixture was dispensed to MA400 PR Streptavidin Plates (Meso Scale Discovery). After the reaction was further performed at room temperature for one hour and washed, Read Buffer T(x4)(Meso Scale Discovery) was dispensed. Immediately after that, measurement was performed by SECTOR PR 400 reader (Meso Scale Discovery). The concentration of hSIL-6R was computationally obtained based on the value shown in a calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). A change of hsIL-6R concentration with time in plasma of a normal mouse after intravenous injection measured by use of this method is shown in
The in-vivo test results of GL1-IgG1_kif+ and GL5-IgG1_kif+ (having a mannose sugar chain added) were compared. As shown in
A variant was prepared by use of QuikChange Site-Directed Mutagenesis Kit (Stratagene) in accordance with the method instructed in the accompanying protocol. The obtained plasmid fragment was inserted in an animal cell expression vector to prepare a target H-chain expression vector and L-chain expression vector. The nucleotide sequences of the obtained expression vectors were determined by a method known to those skilled in the art.
The expression vector prepared was temporarily introduced into a human fetus kidney cancer cell-derived HEK293H strain (Invitrogen) or FreeStyle 293 cell (Invitrogen) to express the antibody. The resultant culture supernatant was collected and passed through a 0.22 μM-filter MILLEX (R)-GV (Millipore) or a 0.45-μM filter MILLEX (R)-GV (Millipore) to obtain a culture supernatant. From the obtained culture supernatant, the antibody was purified by use of rProtein A Sepharose Fast Flow (GE Healthcare) or Protein G Sepharose 4 Fast Flow (GE Healthcare) in accordance with a method known to those skilled in the art. The concentration of the purified antibody was obtained by measuring absorbance by a spectrophotometer at 280 nm and obtaining the concentration of the antibody from the obtained value, by use of an absorption constant calculated by a PACE method (Protein Science (1995) 4, 2411-2423).
A recombinant human IL-6 receptor serving as an antigen was prepared as follows. A cell strain constantly expressing CHO of a soluble human IL-6 receptor ((hereinafter, hsIL-6R) reported by J. Immunol. 152, 4958-4968 (1994)), consisting of an amino acid sequence having 1st to 357th amino acids from the N terminal side was constructed in accordance with a method known to those skilled in the art and cultured to express hsIL-6R. From the resultant culture supernatant, hsIL-6R was purified by two steps, i.e., Blue Sepharose 6 FF column chromatography and gel filtration column chromatography. In the final step, a fraction eluted as a main peak was employed as a final purified product.
A plurality of human antibody phage display libraries displaying Fab domains each consisting of a human antibody sequence were constructed by polyA RNA prepared from human PBMC or commercially available human polyA RNA, etc. as a template, in accordance with a method shown in Mol. Biol. (2002) 178, 87-100.
Acquisition of Ca-Dependent Binding Antibody Fragment from Library by Beads Panning
In the first screening from the human antibody phage display library constructed, only antibody fragments having a binding ability to an antigen were concentrated or concentrated based on Ca-dependent binding ability. When the antibody fragments having a Ca-dependent binding ability were concentrated, the antibody fragments were allowed to bind to an antigen in the presence of Ca ions and then Ca ions were chelated by EDTA. In this manner, phages were eluted. As the antigen, a biotin-labelled human IL-6 receptor was used.
Phages were produced from Escherichia coli harboring a phage-display phagemid constructed as mentioned above. The obtained culture fluid was subjected to precipitation with 2.5 M NaCl/10% PEG and then diluted with TBS to obtain a phage library liquid. To the phage library liquid, BSA and CaCl2 were added so as to obtain a final BSA concentration of 4% and a calcium-ion concentration of 1.2 mM. Panning was performed with reference to a general method using an antigen immobilized to magnetic beads (J Immunol. Methods. (J. Immunol. Methods. (2008) 332 (1-2), 2-9, J Immunol. Methods. (2001) 247 (1-2), 191-203, Biotechnol. Prog. (2002) 18 (2), 212-220, Mol. Cell. Proteomics. (2003) 2 (2), 61-69). As the magnetic beads, NeutrAvidin coated beads (Sera-Mag SpeedBeads NeutrAvidin-coated) or Streptavidin coated beads (Dynabeads M-280 Streptavidin) were used.
More specifically, to the phage library liquid prepared, a biotin-labelled antigen (250 pmol) was added to allow the antigen in contact with the phage library liquid at room temperature for 60 minutes. Then, magnetic beads were blocked with BSA and added at room temperature. Binding was performed at room temperature for 15 minutes. The beads were washed once with 1 mL of 1.2 mM CaCl2/TBS (TBS containing 1.2 mM CaCl2). Thereafter, if antigen fragments having a binding ability were concentrated, elution was performed in accordance with a general method. If antibody fragments having a Ca-dependent binding ability were concentrated, the beads were suspended in 2 mM EDTA/TBS (TBS containing 2 mM EDTA) to recover the phages. To the phage solution recovered, Escherichia coli strain TG1 (10 mL), which reached a logarithm growth phase (OD600 0.4-0.7), was added. A culture was performed while gentry stirring at 37° C. for one hour to infect Escherichia coli cells with the phage. The Escherichia coli cells infected were smeared on a plate of 225 mm×225 mm. Phage was cultured again starting from culturing of the Escherichia coli cells.
In the steps on and after the second panning step, concentration was performed based on a Ca-dependent binding ability. Specifically, to the phage library liquid prepared, biotin-labelled antigen (40 pmol) was added to allow the antigen in contact with the phage library liquid at room temperature for 60 minutes. Then, magnetic beads were blocked with BSA and added at room temperature. Binding was made at room temperature for 15 minutes. The beads were washed once separately with 1 mL of 1.2 mM CaCl2/TBST (TBS containing 1.2 mM CaCl2, 0.1% Tween-20) and 1.2 mM CaCl2/TBS. Thereafter 0.1 mL of 2 mM EDTA/TBS (TBS containing 2 mM EDTA) was added to suspend the beads at room temperature. Immediately after that, the beads were separated by use of Magnet Stand to collect a phage solution. The phage solution collected was added to Escherichia coli strain TG1 (10 mL), which reached a logarithm growth phase (OD600 0.4-0.7)1, and cultured while gentry stirring at 37° C. for one hour to infect Escherichia coli cells with the phase. The Escherichia coli cells infected were smeared on a plate of 225 mm×225 mm. Phage was cultured again starting from culturing of the Escherichia coli cells. The panning step was repeated twice.
From a single colony of Escherichia coli obtained by the above method, a phage-containing culture supernatant was recovered in accordance with the method (Methods Mol. Biol. (2002) 178, 133-145). To the phage-containing culture supernatant, BSA and CaCl2 were added so as to obtain a final BSA concentration of 4% and a calcium-ion concentration of 1.2 mM. The resultant mixture was subjected to ELISA. A StreptaWell 96 microtiter plate (Roche) was coated with PBS (100 μL) containing the biotin-labelled antigen overnight, washed with PBST (PBS containing 0.1% Tween20) to remove the antigen. Thereafter blocking was performed with 4% BSA-TBS (250 μL) for one hour or more. Then, 4% BSA-TBS was removed and the culture supernatant prepared was added. The mixture was allowed to stand still at 37° C. for one hour. In this way, binding of the phage displaying antibody was made. After washing with 1.2 mM CaCl2/TBST (TBS containing 1.2 mM CaCl2 and 0.1% Tween20), 1.2 mM CaCl2/TBS or 1 mM EDTA/TBS was added. The mixture was allowed to stand still at 37° C. for 30 minutes to incubate. After washing with 1.2 mM CaCl2/TBST, HRP-binding anti M13 antibody (Amersham Parmacia Biotech) diluted with TBS containing 4% BSA and a calcium ion at a concentration of 1.2 mM was incubated for one hour. After washing with 1.2 mM CaCl2/TBST, detection was made with a TMB single solution (ZYMED). After the reaction was terminated with sulfuric acid, the absorbance at 450 nm was measured. The antibody fragments determined to have a Ca-dependent binding ability were subjected to nucleotide sequence analysis using a specific primer.
A clone, which was determined to have a Ca-dependent binding ability by phage ELISA, was introduced into an animal cell expression plasmid. Expression of an antibody was performed by the following method. A human fetus kidney cell-derived FreeStyle 293-F strain (Invitrogen) was suspended in FreeStyle 293 Expression Medium (Invitrogen). The suspension solution (3 mL) was seeded in each well of a 6 well plate at a cell density of 1.33×106 cells/mL and a plasmid prepared was introduced into the cell by a lipofection method. Culture was made in a CO2 incubator (37° C., 8% CO2, 90 rpm) for 4 days. From the obtained culture supernatant, an antibody was purified by use of rProtein A Sepharose™ Fast Flow (Amersham Biosciences) in accordance with a method known to those skilled in the art. The concentration of the purified antibody was determined based on the absorbance at 280 nm measured by a spectrophotometer. From the obtained measurement value, an antibody concentration was computationally obtained by use of the absorption constant calculated by the PACE method (Protein Science (1995) 4, 2411-2423).
To determine whether the antibody obtained in Reference Example 4, i.e., 6RL#9-IgG1 (heavy chain SEQ ID NO: 7, light chain SEQ ID NO: 39), and FH4-IgG1 (heavy chain SEQ ID NO: 40, light chain SEQ ID NO: 41), have a Ca-dependent binding ability, kinetic analysis of an antigen-antibody reaction was performed by use of Biacore T100 (GE Healthcare). The above heavy-chain variable region was fused with an IgG1 constant region (having a deletion of 2 amino acids at the C terminal of SEQ ID NO: 9) to prepare a heavy chain sequence. Furthermore, a light-chain variable region (SEQ ID NO: 41) was fused with a constant region of light-chain k chain (SEQ ID NO: 42) to prepare a light chain sequence. As an antibody having no Ca dependency, H54/L28-IgG1 (heavy chain SEQ ID NO: 26, light chain SEQ ID NO: 27) described in WO 2009/125825 was used. As a high calcium-ion concentration, 2 mM was used and as a low calcium-ion concentration, 3 μM was used. As the antigen, a human IL-6 receptor (IL-6R) was used. An appropriate amount of protein A (Invitrogen) was immobilized onto Sensor chip CM4 (GE Healthcare) in accordance with the amine coupling method and then a target antibody was allowed to capture. Either one of two types of running buffers, i.e., 10 mmol/L ACES, 150 mmol/L NaCl, 0.05% (w/v) Tween20, 2 mmol/L CaCl2, (pH 7.4) and 10 mmol/L ACES, 150 mmol/L NaCl, 0.05% (w/v) Tween20, 3 μMol/L CaCl2, (pH 7.4) was used. All samples were measured at 37° C. Each buffer was employed for dilution of IL-6R.
With respect to H54L28-IgG1, an IL-6R dilution solution and a running buffer (a blank) were injected at a flow rate 20 μL/min for 3 minutes and allowed IL-6R to interact with the antibody captured onto a sensor chip. Thereafter, the running buffer was fed at a flow rate of 20 μL/min for 10 minutes. After dissociation of IL-6R was observed, 10 mmol/L Glycine-HCl, pH 1.5 was injected at a flow rate 30 μL/min for 30 seconds to regenerate the sensor chip. From the sensorgram obtained by measurement, an association constant, ka (1/Ms) and a dissociation constant kd (1/s) as kinetics parameters were computationally obtained. From the values, KD (M) of each antibody to a human IL-6 receptor was calculated. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare).
With respect to FH4-IgG1 and 6RL#9-IgG1, an IL-6R dilution solution and the running buffer (a blank) were injected at a flow rate 5 μL/min for 15 minutes and allowed IL-6R to interact with the antibody captured onto a sensor chip. Thereafter, 10 mmol/L Glycine-HCl, pH 1.5 was injected at a flow rate of 30 μL/min for 30 seconds to regenerate the sensor chip. From the sensorgram obtained by measurement, an association constant, a dissociation constant KD (M) was obtained by a steady state affinity model. Individual parameters were calculated by use of Biacore T100 Evaluation Software (GE Healthcare).
The dissociation constant KD between each antibody and IL-6R obtained by this method in the presence of 2 mM CaCl2 is shown in Table 7. In the case of H54/L28-IgG1, any difference was not observed in binding to IL-6R in different Ca concentrations; however in the cases of FH4-IgG1 and 6RL#9-IgG1, binding significantly decreased under a low Ca concentration condition (
With respect to H54/L28-IgG1, KD under a Ca concentration of 3 μM can be calculated in the same manner as under 2 mM Ca concentration. With respect to FH4-IgG1 and 6RL#9-IgG1, if a Ca concentration of 3 μM, binding to IL-6R was not virtually observed. Thus, it is difficult to calculate KD in accordance with the aforementioned method; however, KD can be estimated by use of the following Expression 1 (Biacore T100 Software Handbook, BR-1006-48, AE 01/2007).
Req=C·Rmax/(KD+C)+RI [Expression 1]
where
Req (RU): Steady state binding levels
Rmax (RU): Analyte binding capacity of the surface
RI (RU): Bulk refractive index contribution in the sample
C (M): Analyte concentration
KD (M): Equilibrium dissociation constant
Presumable dissociation constant KD between each antibody and IL-6R was roughly calculated in accordance with Expression 1 in the case of a Ca concentration of 3 μMol/L. The results are shown in Table 8.
In Table 8, Req, Rmax, RI and C are estimated from measurement results.
From the results, it was estimated that in FH4-IgG1 and 6RL#9-IgG1, KD values of them to IL-6R may increase approximately 60 fold and approximately 120 fold, (affinity may decrease 60 fold, 120 fold or more) affinity) respectively by changing the concentration of Ca from 2 mM to 3 μM in terms of CaCl2. KD values of three antibodies: H54/L28-IgG1, FH4-IgG1 and 6RL#9-IgG1 in the presence of 2 mMCaCl2 and 3 μM CaCl2 and Ca dependency of the KD value are summarized in Table 9.
Calcium ion-binding to an antibody was evaluated based on the thermal denaturation mid-temperature (Tm value) measured by differential scanning calorimetry (DSC) (MicroCal VP-Capillary DSC, manufactured by MicroCal). The thermal denaturation intermediate temperature (Tm value) is used as an index of stability. When a protein is stabilized by binding of a calcium ion, the thermal denaturation intermediate temperature (Tm value) increases compared to the protein to which a calcium ion is not bound (J. Biol. Chem. (2008) 283 (37) 25140-25149). By using this phenomenon, calcium ion-binding to an antibody was evaluated. The antibody purified was dialyzed against a solution containing 20 mM Tris-HCl, 150 mM NaCl and 2 mM CaCl2, pH 7.4, or a solution containing 20 mM Tris-HCl, 150 mM NaCl and 3 μM CaCl2, pH 7.4 by use of EasySEP, (TOMY). A protein solution was prepared with the solution used in dialysis so as to obtain concentration of 0.1 mg/mL and then subjected to DSC measurement by raising temperature from 20° C. to 115° C. at a rate of 240° C./hr. The thermal denaturation intermediate temperature (Tm value) of a Fab domain of each antibody based on the DSC denaturation curve obtained was calculated and is shown in Table 10.
From the results of Table 10, it was shown that, in the cases of FH4 and 6RL#9 showing a calcium-dependent binding ability, the Tm value of Fab changes depending upon the calcium-ion concentration; whereas, in H54/L28 showing no calcium-dependent binding ability, the Tm value does not change. A change of the Tm value of Fab shown in FH4 and 6RL#9 suggests that a calcium ion binds to these antibodies to stabilize the Fab domain thereof. From this, it was demonstrated that a calcium ion binds to FH4 and 6RL#9; whereas calcium ion is not bound to H54/L28.
To a normal mouse (C57BL/6J mouse, Charles River Japan) hsIL-6R (soluble human IL-6 receptor prepared in Reference Example 3) was solely administered or hsIL-6R and an anti-human IL-6 receptor antibody were simultaneously administered. Thereafter, in-vivo kinetics of the hsIL-6R and the anti-human IL-6 receptor antibody was evaluated. A hsIL-6R solution (5 μg/mL) or a mixture solution of the hsIL-6R and the anti-human IL-6 receptor antibody was administered once to caudal vein in a dose of 10 mL/kg. As the anti-human IL-6 receptor antibody, the aforementioned H54/L28-IgG1, 6RL#9-IgG1 and FH4-IgG1 were used.
The hsIL-6R concentrations of the mixture solutions are all 5 μg/mL, the anti-human IL-6 receptor antibody concentration varies depending upon the antibody. The concentration of H54/L28-IgG1 is 0.1 mg/mL and the concentrations of 6RL#9-IgG1 and FH4-IgG1 are 10 mg/mL. At this time, since anti-human IL-6 receptor antibody is excessively present compared to hsIL-6R, it is considered that almost all hsIL-6R molecules bind to the antibody. Blood was sampled 15 minutes, 7 hours, 1 day, 2 days, 3 days, 4 days, 7 days, 14 days, 21 days, 28 days after the administration. The blood sampled was immediately centrifuged at 4° C., 12,000 rpm for 15 minutes to obtain plasma. The plasma separated was stored in a freezer set at −20° C. or less until measurement.
The concentration of an anti-human IL-6 receptor antibody in mouse plasma was measured by ELISA. First, Anti-Human IgG (γ-chain specific) F(ab′)2 Fragment of Antibody (SIGMA) was dispensed in Nunc-Immuno Plates, MaxiSoup (Nalge nunc International). The mixture was allowed to stand still at 4° C. overnight to prepare an Anti-Human IgG immobilized plates. Samples having a plasma concentration of 0.64, 0.32, 0.16, 0.08, 0.04, 0.02, and 0.01 μg/mL were prepared for forming a calibration curve sample and a mouse plasma measurement sample diluted 100 fold or more were prepared, dispensed in Anti-Human IgG immobilized plates and incubated at 25° C. for one hour. Thereafter, Biotinylated Anti-human IL-6R Antibody (R&D) was reacted at room temperature for one hour and then, Streptavidin-PolyHRP80 (Stereospecific Detection Technologies) was reacted at 25° C. for 0.5 hours. A chromogenic reaction was performed using TMB One Component HRP Microwell Substrate (BioFX Laboratories) as a substrate and terminated with 1N-Sulfuric acid (Showa Chemical). Thereafter, the absorbance at 450 nm was measured by a micro plate reader. The concentration in the mouse plasma was computationally obtained from the absorbance shown in the calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). Changes of H54/L28-IgG1, 6RL#9-IgG1, FH4-IgG1 antibody concentration with time in normal mouse plasma after intravenous administration measured by this method are shown in
Measurement of hsIL-6R Concentration in Plasma by Electrochemiluminescence Assay
Concentration of hsIL-6R in mouse plasma was measured by electrochemiluminescence assay. Samples of hsIL-6R having a concentration of 2000, 1000, 500, 250, 125, 62.5 and 31.25 pg/mL were prepared and a mouse plasma measurement sample diluted to 50 fold or more was prepared. Monoclonal Anti-human IL-6R Antibody (R&D) labeled with ruthenium by means of SULFO-TAG NHS Ester (Meso Scale Discovery), Biotinylated Anti-human IL-6R Antibody (R&D), and a tocilizumab (heavy chain SEQ ID NO: 37, light chain SEQ ID NO: 38) solution were mixed and reacted at 4° C. overnight. At this time, 10 mM EDTA was added to the Assay buffer in order to decrease Free Ca concentration in a sample, thereby dissociating almost all hsIL-6R molecules from 6RL#9-IgG1 or FH4-IgG1 and associating with tocilizumab added. Thereafter, the mixture was dispensed to MA400 PR Streptavidin Plates (Meso Scale Discovery). Furthermore, a reaction was performed at 25° C. for one hour and Read Buffer T (x4) (Meso Scale Discovery) was dispensed. Immediately after that, measurement was performed by SECTOR PR 400 reader (Meso Scale Discovery). The concentration of hSIL-6R was computationally obtained based on the value shown in a calibration curve by use of analytic software SOFTmax PRO (Molecular Devices). A change of hsIL-6R concentration with time in plasma of a normal mouse after intravenous injection measured by this method is shown in
As a result, in the case of single administration of hsIL-6R, hsIL-6R was cleared at an extremely high speed; whereas, in the simultaneous administration of hsIL-6R and a general antibody H54/L28-IgG1 (no Ca-dependent binding), the clearance speed of hsIL-6R was significantly low. In contrast, in the case of simultaneous administration of 6RL#9-IgG1 or FH4-IgG1 (showing Ca-dependent binding to hsIL-6R (100 fold or more)) and hsIL-6R, the clearance speed was significantly accelerated. In the simultaneous administration cases with 6RL#9-IgG1 and FH4-IgG1, compared to simultaneous administration with H54/L28-IgG1, the hsIL-6R concentration of Day 1 in plasma was successfully reduced 39 fold and 2 fold, respectively. From this, it was confirmed that a calcium-dependent binding antibody can accelerate clearance of an antigen from the plasma.
As shown in Reference Example 6, the thermal denaturation temperature Tm assay suggested that the 6RL#9 antibody bound to calcium ions. However, the site via which the 6RL#9 antibody bound to calcium ions was unpredictable. Thus, a residue responsible for the interaction with calcium ions was identified in the sequence of the 6RL#9 antibody by use of the approach of X-ray crystal structure analysis.
The 6RL#9 antibody expressed for use in X-ray crystal structure analysis was purified. Specifically, animal cells were transiently transfected with plasmids for expression in animal cells prepared so as to permit respective expression of the heavy chain and the light chain of the 6RL#9 antibody as shown in Reference Example 5. The prepared plasmids were transferred by lipofection to 800 mL of a human embryonic kidney cell-derived FreeStyle 293-F line (Invitrogen Corp.) suspended at a final cell density of 1×106 cells/mL in FreeStyle 293 Expression Medium (Invitrogen Corp.). The cells transfected with the plasmids were cultured for 5 days in a CO2 incubator (37° C., 8% CO2, 90 rpm). Antibodies were purified from the obtained culture supernatant according to a method generally known to those skilled in the art using rProtein A Sepharose™ Fast Flow (Amersham Biosciences, Inc.). The absorbance of the purified antibody solution was measured at 280 nm using a spectrophotometer. The antibody concentration was calculated from the measurement value by use of an extinction coefficient calculated by PACE (Protein Science (1995) 4, 2411-2423).
Purification of Fab Fragment from 6RL#9 Antibody
The 6RL#9 antibody was concentrated to 21 mg/mL using an ultrafiltration membrane having a molecular weight cutoff of 10000 MWCO. The antibody was diluted to 5 mg/mL with 4 mM L-cysteine, 5 mM EDTA, and a 20 mM sodium phosphate buffer solution (pH 6.5) to prepare 2.5 mL of an antibody sample. After addition of 0.125 mg of papain (Roche Applied Science), the sample was stirred and then left standing at 35° C. for 2 hours. The sample thus left standing was further supplemented with one tablet of Protease Inhibitor Cocktail Mini, EDTA-Free (Roche Applied Science) dissolved in 10 mL of a 25 mM MES buffer solution (pH 6), and left standing in ice to terminate the protease reaction with papain. Next, the sample was added to a 1 mL-size cation-exchange column HiTrap SP HP (GE Healthcare Bio-Sciences Corp.) (equilibrated with a 25 mM MES buffer solution (pH 6)) connected in tandem with a downstream 1 mL-size protein A carrier column HiTrap MabSelect Sure (GE Healthcare Bio-Sciences Corp.). A purified fraction of the 6RL#9 antibody Fab fragment was obtained by elution on a linear gradient of NaCl concentration up to 300 mM in this buffer solution. Next, the obtained purified fraction was concentrated to approximately 0.8 mL using a 5000 MWCO ultrafiltration membrane. The concentrate was added to a gel filtration column Superdex 200 10/300 GL (GE Healthcare Bio-Sciences Corp.) equilibrated with a 100 mM HEPES buffer solution (pH 8) containing 50 mM NaCl. The purified 6RL#9 antibody Fab fragment for crystallization was eluted from the column using this buffer solution. The column operation was all carried out at a low temperature of 6 to 7.5° C.
Seed crystals of the 6RL#9 Fab fragment were obtained in advance under generally set conditions. Next, the purified 6RL#9 antibody Fab fragment was adjusted to 5 mM by the addition of CaCl2 and concentrated to 12 mg/mL using a 5000 MWCO ultrafiltration membrane. Subsequently, the sample thus concentrated was crystallized by the hanging-drop vapor diffusion method. A 100 mM HEPES buffer solution (pH 7.5) containing 20 to 29% PEG4000 was used as a reservoir solution. The seed crystals were disrupted in a 100 mM HEPES buffer solution (pH 7.5) containing 29% PEG4000 and 5 mM CaCl2 and diluted 100- to 10000-fold, and 0.2 μl of each solution of this dilution series was added to a mixed solution of 0.8 μl of the reservoir solution and 0.8 μl of the concentrated sample on a glass cover to prepare crystallization drops. The crystallization drops were left standing at 20° C. for 2 days to 3 days. X-ray diffraction data on the obtained thin plate-like crystals was determined.
The purified 6RL#9 antibody Fab fragment was concentrated to 15 mg/mL using a 5000 MWCO ultrafiltration membrane. Subsequently, the sample thus concentrated was crystallized by the hanging-drop vapor diffusion method. A 100 mM HEPES buffer solution (pH 7.5) containing 18 to 25% PEG4000 was used as a reservoir solution. Crystals of the 6RL#9 antibody Fab fragment obtained in the presence of Ca were disrupted in a 100 mM HEPES buffer solution (pH 7.5) containing 25% PEG4000 and diluted 100- to 10000-fold, and 0.2 μl of each solution of this dilution series was added to a mixed solution of 0.8 μl of the reservoir solution and 0.8 μl of the concentrated sample on a glass cover to prepare crystallization drops. The crystallization drops were left standing at 20° C. for 2 days to 3 days. X-ray diffraction data on the obtained thin plate-like crystals was assayed.
One of the monocrystals (obtained in the presence of Ca) of the 6RL#9 antibody Fab fragment dipped in a 100 mM HEPES buffer solution (pH 7.5) containing 35% PEG4000 and 5 mM CaCl2 was scooped out, together with the external solution, using very small nylon loop pin and frozen in liquid nitrogen. The X-ray diffraction data on the frozen crystal was assayed using beam line BL-17A from Photon Factory, Institute Materials Structure Science, High Energy Accelerator Research Organization (KEK). During the assay, the frozen crystal was left at all times in a nitrogen stream of −178° C. to maintain its frozen state. A total of 180 diffraction images were collected, with the crystal rotated by 1° for each image, using a CCD detector Quantum 315r (Area Detector Systems Corporation (ADSC)) equipped with the beam line. The determination of a lattice constant, the indexing of diffraction spots, and the processing of the diffraction date were performed using a program Xia2 (CCP4 Software Suite), XDS Package (Wolfgang Kabsch), and Scala (CCP4 Software Suite). Finally, diffraction intensity data up to a resolution of 2.2 angstroms was obtained. This crystal belonged to the space group P212121 and had lattice constants a=45.47 angstroms, b=79.86 angstroms, c=116.25 angstroms, α=90°, β=90°, and γ=90°.
One of the monocrystals (obtained in the absence of Ca) of the 6RL#9 antibody Fab fragment dipped in a 100 mM HEPES buffer solution (pH 7.5) containing 35% PEG4000 was scooped out, together with the external solution, using very small nylon loop pin and frozen in liquid nitrogen. The X-ray diffraction data on the frozen crystal was assayed using beam line BL-5A from Photon Factory, Institute Materials Structure Science, High Energy Accelerator Research Organization (KEK). During the assay, the frozen crystal was left at all times in a nitrogen stream of −178° C. to maintain its frozen state. A total of 180 diffraction images were collected, with the crystal rotated by 1° for each image, using a CCD detector Quantum 210r (Area Detector Systems Corporation (ADSC)) equipped with the beam line. The determination of a lattice constant, the indexing of diffraction spots, and the processing of the diffraction date were performed using a program Xia2 (CCP4 Software Suite), XDS Package (Wolfgang Kabsch), and Scala (CCP4 Software Suite). Finally, diffraction intensity data up to a resolution of 2.3 angstroms was obtained. This crystal, which was the same type of the crystal obtained in the presence of Ca, belonged to the space group β212121 and had lattice constants a=45.40 angstroms, b=79.63 angstroms, c=116.07 angstroms, α=90°, β=90°, and γ=90°.
The structure of the crystal of the 6RL#9 antibody Fab fragment obtained in the presence of Ca was determined by the molecular replacement method using a program Phaser (CCP4 Software Suite). The number of molecules in the asymmetric unit was presumed to be one from the size of the obtained crystal lattice and the molecular weight of the 6RL#9 antibody Fab fragment. On the basis of homology on the primary sequence, amino acid residues at positions 112 to 220 in the chain A and at positions 116 to 218 in the chain B retrieved from the structure coordinate of PDB code: 1ZA6 were selected as model molecules for search for CL and CH1 regions. Next, amino acid residues at positions 1 to 115 in the chain B retrieved from the structure coordinate of PDB code: 1ZA6 were selected as a model molecule for search for a VH region. Finally, amino acid residues at positions 3 to 147 in the light chain retrieved from the structure coordinate of PDB code: 2A9M were selected as a model molecule for search for a VL region. According to this order, the orientation and position of each model molecule for search in the crystal lattice were determined by rotation and translation functions to obtain an initial structural model of the 6RL#9 antibody Fab fragment. The initial structural model was subjected to rigid body refinement moving each of the VH, VL, CH1, and CL domains to obtain a crystallographic reliability factor R of 46.9% and a Free R value of 48.6% for reflection data of 25-3.0 angstroms. In addition, the model was refined by model correction on a repetition program Coot (Paul Emsley) with reference to electron density maps of coefficients 2Fo-Fc and Fo-Fc calculated through the use of structure refinement using a program Refmac5 (CCP4 Software Suite), an experimentally determined structure factor Fo, a structure factor Fc calculated from the model, and a phase. Final refinement was performed using a program Refmac5 (CCP4 Software Suite) by the incorporation of Ca ion and water molecules into the model on the basis of the electron density maps of coefficients 2Fo-Fc and Fo-Fc. Finally, a crystallographic reliability factor R of 20.0% and a Free R value of 27.9% were obtained for the model of 3440 atoms by use of 21020 reflection data with a resolution of 25-2.2 angstroms.
The structure of the crystal of the 6RL#9 antibody Fab fragment obtained in the absence of Ca was determined using the structure of the crystal, which was the same type thereas, obtained in the presence of Ca. Water and Ca ion molecules were excluded from the structure coordinate of the crystal of the 6RL#9 antibody Fab fragment obtained in the presence of Ca, followed by rigid body refinement moving each of the VH, VL, CH1, and CL domains to obtain a crystallographic reliability factor R of 30.3% and a Free R value of 31.7% for reflection data of 25-3.0 angstroms. In addition, the model was refined by model correction on a repetition program Coot (Paul Emsley) with reference to electron density maps of coefficients 2Fo-Fc and Fo-Fc calculated through the use of structure refinement using a program Refmac5 (CCP4 Software Suite), an experimentally determined structure factor Fo, a structure factor Fc calculated from the model, and a phase. Final refinement was performed using a program Refmac5 (CCP4 Software Suite) by the incorporation of water molecules into the model on the basis of the electron density maps of coefficients 2Fo-Fc and Fo-Fc. Finally, a crystallographic reliability factor R of 20.9% and a Free R value of 27.7% were obtained for the model of 3351 atoms by use of 18357 reflection data with a resolution of 25-2.3 angstroms.
As a result of structural comparison between the crystals of the 6RL#9 antibody Fab fragment obtained in the presence of Ca and in the absence of Ca, large change was seen in heavy chain CDR3.
A human antibody phage display library consisting of a plurality of phages displaying Fab domains having distinct human antibody sequences was constructed according to a method generally known to those skilled in the art using poly-A RNA prepared from human PBMC, commercially available human poly-A RNA, or the like as a template.
Obtainment of Antibody Fragment Binding to Antigen in Ca-Dependent Manner from Library by Bead Panning
The first round of screening of the constructed naive human antibody phage display library was carried out by the enrichment of only antibody fragments having antigen (IL-6)-binding ability. The antigens used were biotin-labeled IL-6. Phages were produced from Escherichia coli harboring a phage display phagemid constructed. To the obtained culture fluid of Escherichia coli producing phage, 2.5 M NaCl/10% PEG was added to precipitate phages. The precipitate phages were diluted with TBS to obtain a phage library liquid. Then, to the phage library liquid, BSA and CaCl2 were added so as to obtain a final BSA concentration of 4% and a calcium-ion concentration of 1.2 mM. Panning was performed with reference to a general method using an antigen immobilized to magnetic beads (J. Immunol. Methods. (2008) 332 (1-2), 2-9, J. Immunol. Methods. (2001) 247 (1-2), 191-203, Biotechnol. Prog. (2002) 18 (2) 212-20, Mol. Cell Proteomics (2003) 2 (2), 61-9). As the magnetic beads, NeutrAvidin coated beads (Sera-Mag SpeedBeads NeutrAvidin-coated) or Streptavidin coated beads (Dynabeads M-280 Streptavidin) were used.
Specifically, 250 pmol of biotin-labeled antigens was added to the prepared phage library solution and thereby contacted with the phage library solution at room temperature for 60 minutes. After addition of BSA-blocked magnetic beads, the antigen-phage complexes were attached to the magnetic beads at room temperature for 15 minutes. The beads were washed three times with 1.2 mM CaCl2/TBST (TBST containing 1.2 mM CaCl2) and then further washed twice with 1 mL of 1.2 mM CaCl2/TBS (TBS containing 1.2 mM CaCl2). After addition of 0.5 mL of 1 mg/mL trypsin, the beads were suspended at room temperature for 15 minutes, immediately after which the beads were separated using a magnetic stand to recover a phage solution. The recovered phage solution was added to 10 mL of an E. coli strain TG1 in a logarithmic growth phase (OD600: 0.4-0.7). The E. coli strain was infected by the phages through the gentle spinner culture of the strain at 37° C. for 1 hour. The infected E. coli was inoculated to a plate of 225 mm×225 mm. Next, phages were recovered from cultures of the inoculated E. coli to prepare a phage library solution.
In the second and subsequent rounds of panning, the phages were enriched with Ca-dependent binding ability as an index. Specifically, 40 pmol of biotin-labeled antigens was added to the prepared phage library solution and thereby contacted with the phage library solution at room temperature for 60 minutes. After addition of BSA-blocked magnetic beads, the antigen-phage complexes were attached to the magnetic beads at room temperature for 15 minutes. The beads were washed with 1 mL of 1.2 mM CaCl2/TBST and 1.2 mM CaCl2/TBS. Then, the beads supplemented with 0.1 mL of 2 mM EDTA/TBS were suspended at room temperature. Immediately thereafter, the beads were separated using a magnetic stand to recover a phage solution. The addition of 5 μL of 100 mg/mL trypsin to the recovered phage solution cleaved the pIII proteins (helper phage-derived pIII proteins) of non-Fab-displaying phages to cancel the ability of the non-Fab-displaying phages to infect E. coli. The phages recovered from the trypsin-treated phage solution were added to 10 mL of an E. coli strain TG1 in a logarithmic growth phase (OD600: 0.4-0.7). The E. coli strain was infected by the phages through the gentle spinner culture of the strain at 37° C. for 1 hour. The infected E. coli was inoculated to a plate of 225 mm×225 mm. Next, phages were recovered from cultures of the inoculated E. coli to recover a phage library solution. This panning with Ca-dependent binding ability as an index was performed 3 rounds in total.
A phage-containing culture supernatant was recovered according to a conventional method (Methods Mol. Biol. (2002) 178, 133-145) from each single colony of the E. coli obtained by the above method. After addition of BSA and CaCl2 (final concentration: 4% BSA and 1.2 mM calcium ion), the phage-containing culture supernatant was subjected to ELISA by the following procedures: StreptaWell 96 microtiter plate (F. Hoffmann-La Roche Ltd.) was coated overnight with 100 μL of PBS containing biotin-labeled antigens. Each well of the plate was washed with PBST to remove unbound antigens. Then, the well was blocked with 250 μL of 4% BSA-TBS for 1 hour or longer. After removal of 4% BSA-TBS, the prepared culture supernatant was added to each well, and the plate was left standing at 37° C. for 1 hour to associate phage-displayed antibodies with the antigens contained in each well. Each well was washed with 1.2 mM CaCl2/TBST, and 1.2 mM CaCl2/TBS or 1 mM EDTA/TBS was added thereto. The plate was left standing at 37° C. for 30 minutes for incubation. After washing with 1.2 mM CaCl2/TBST, HRP-conjugated anti-M13 antibodies (Amersham Pharmacia Biotech Inc.) diluted with TBS having 4% BSA and an ionized calcium concentration of 1.2 mM (all were indicated by final concentrations) were added to each well. The plate was incubated for 1 hour. After washing with 1.2 mM CaCl2/TBST, TMB single solution (ZYMED Laboratories, Inc.) was added to the well. The chromogenic reaction of the solution in each well was terminated by the addition of sulfuric acid. Then, the developed color was assayed on the basis of absorbance at 450 nm.
A 6KC4-1#85 antibody having Ca-dependent IL-6-binding ability was obtained by phage ELISA using 96 isolated clones. The gene of the antibody fragment judged as having Ca-dependent antigen-binding ability as a result of the phage ELISA was amplified as a template using specific primers and then analyzed for its nucleotide sequence. The sequence of the heavy chain variable region of the 6KC4-1#85 antibody is shown in SEQ ID NO: 8, and the sequence of the light chain variable region thereof is shown in SEQ ID NO: 43. A polynucleotide encoding the heavy chain variable region (SEQ ID NO: 8) of the 6KC4-1#85 antibody was linked by PCR to a polynucleotide encoding an IgG1-derived sequence. The resulting DNA fragment was incorporated into vectors for expression in animal cells to construct vectors that permits expression of a heavy chain represented by SEQ ID NO: 44. A polynucleotide encoding the light chain variable region (SEQ ID NO: 43) of the 6KC4-1#85 antibody was linked by PCR to a polynucleotide encoding a natural kappa chain constant region (SEQ ID NO: 42). The resulting DNA fragment encoding the sequence represented by SEQ ID NO: 45 was incorporated into vectors for expression in animal cells. The sequence of the prepared modified form was confirmed by a method generally known to those skilled in the art. The sequence of the prepared modified form was confirmed by a method generally known to those skilled in the art.
The gene of the clone 6KC4-1#85 judged as having Ca-dependent antigen-binding ability as a result of the phage ELISA was introduced to plasmids for expression in animal cells. Antibody expression was performed by the following method: a human embryonic kidney cell-derived FreeStyle 293-F line (Invitrogen Corp.) was suspended in FreeStyle 293 Expression Medium (Invitrogen Corp.). The suspension having a cell density of 1.33×106 cells/mL was inoculated at a concentration of 3 mL/well to a 6-well plate. The prepared plasmids were transferred to the cells by lipofection. The cells were cultured for 4 days in a CO2 incubator (37° C., 8% CO2, 90 rpm). Antibodies were purified from the obtained culture supernatant by a method generally known to those skilled in the art using rProtein A Sepharose™ Fast Flow (Amersham Biosciences, Inc.). The absorbance of the purified antibody solution was measured at 280 nm using a spectrophotometer. The antibody concentration was calculated from the obtained measurement value by use of an extinction coefficient calculated by PACE (Protein Science (1995) 4, 2411-2423).
The calcium-dependent antigen-binding antibody 6KC4-1#85 obtained from the human antibody library was evaluated for its calcium binding. Whether or not a measured Tm value varied under different ionized calcium concentrations was evaluated by the method described in Reference Example 6.
Table 11 shows the Tm value of the Fab domain of the 6KC4-1#85 antibody. As shown in Table 11, the Tm value of the Fab domain of the 6KC4-1#85 antibody varied depending on calcium ion concentration, demonstrating that the 6KC4-1#85 antibody binds to calcium.
In Example 10, it was shown that 6KC4-1#85 antibody binds to a calcium ion; however, 6KC4-1#85 does not have a calcium-binding motif such as an hVk5-2 sequence. Then, to identify the residue of the 6KC4-1#85 antibody to which a calcium ion binds, the Asp (D) residue present in CDR of the 6KC4-1#85 antibody was substituted with Ala (A) residue, which is not involved in binding or chelating of a calcium ion, to prepare modified heavy chains (6_H1-11 (SEQ ID NO: 46), 6_H1-12 (SEQ ID NO: 47), 6_H1-13 (SEQ ID NO: 48), 6_H1-14 (SEQ ID NO: 49), 6_H1-15 (SEQ ID NO: 50)) and modified light chains (6_L1-5 (SEQ ID NO: 51) and 6_L1-6 (SEQ ID NO: 52)). A modified antibody gene was introduced into an expression vector, which was further introduced into an animal cell. The animal cell was cultured. From the culture fluid, a modified antibody was purified in accordance with the method described in Example 4. Calcium binding of the modified antibody purified was determined by the method described in Example 6. The measurement results are shown in Table 12.
As shown in Table 12, 6KC4-1#85 antibody loses a calcium binding ability by substituting position 95, or position 101 (Kabat numbering) of heavy-chain CDR3 of the 6KC4-1#85 antibody with An Ala residue. From this, it is considered that this residue plays an important role in binding calcium. It was elucidated, from the calcium binding ability of a modified 6KC4-1#85 antibody, that the calcium-binding motif present in the vicinity of the base of a loop of heavy chain CDR3 of the 6KC4-1#85 antibody can be also used as a calcium-binding motif in the antigen-binding domain contained in the antigen-binding molecule of the present invention.
An antibody containing a human genital cell lineage sequence and capable of binding to a calcium ion has not yet been reported up to present. Then, to determine whether an antibody containing a human genital cell lineage sequence binds to a calcium ion or not, the genital cell lineage sequence of an antibody containing a human genital cell lineage sequence was cloned by using cDNA prepared from a Human Fetal Spleen Poly RNA (Clontech) as a template. The cloned DNA fragment was inserted into an animal cell expression vector. The nucleotide sequence of the obtained expression vector was determined in accordance with a method known to those skilled in the art. The number of the sequences are shown in Table 13. The polynucleotides encoding SEQ ID NO: 53 (Vk1), SEQ ID NO: 54 (Vk2), SEQ ID NO: 55 (Vk3), SEQ ID NO: 56 (Vk4) and SEQ ID NO: 6 (Vk5-2) were each ligated to a constant region (SEQ ID NO: 42) encoding a natural Kappa chain by a PCR method. The resultant DNA fragment was integrated into an animal cell expression vector. Furthermore, polynucleotides encoding SEQ ID NO: 57 (Vk1), SEQ ID NO: 58 (Vk2), SEQ ID NO: 59 (Vk3), SEQ ID NO: 60 (Vk4) and SEQ ID NO: 61 (Vk5) were each ligated to a polynucleotide encoding IgG1 (SEQ ID NO: 9) having 2 amino-acid deletion at the C terminal by a PCR method. The resultant DNA fragment was inserted into an animal cell expression vector. The sequences of the modified forms thus prepared were confirmed by a method known to those skilled in the art.
The obtained five DNA fragments having a human genital cell lineage sequence inserted therein were each inserted into an animal cell expression vector, which was then inserted into an animal cell. The antibody was expressed by the following method. A human fetus kidney cell-derived FreeStyle 293-F strain (Invitrogen) was suspended in FreeStyle 293 Expression Medium (Invitrogen). 3 mL of the suspension solution was seeded in each well of a 6 well plate at a cell density of 1.33×106 cells/mL. The plasmid prepared was introduced into the cell by a lipofection method. Culture was performed in a CO2 incubator (37° C., 8% CO2, 90 rpm) for 4 days. From the obtained culture supernatant, an antibody was purified by use of rProtein A Sepharose™ Fast Flow (Amersham Biosciences) in accordance with a method known to those skilled in the art. The absorbance of a solution of the purified antibody was measured by a spectrophotometer. From the obtained measurement value, an antibody concentration was calculated by use of the absorption constant calculated by the PACE method (Protein Science (1995) 4, 2411-2423).
The calcium ion-binding activity of the purified antibodies was evaluated. The purified antibodies were each subjected to dialysis (EasySEP, TOMY) treatment using a solution containing 20 mM Tris-HCl, 150 mM NaCl, 2 mM CaCl2 (pH 7.4) or a solution containing 20 mM Tris-HCl, 150 mM NaCl, 3 μMCaCl2 (pH 7.4) as an external solution. An antibody solution, which was prepared by use of the solution used in dialysis so as to obtain a concentration of approximately 0.1 mg/mL, was used as a test subject, DSC measurement was performed by raising temperature from 20° C. up to 115° C. at a rate of 240° C./hr. The thermal denaturation intermediate temperature (Tm value) of the Fab domain of each antibody was obtained based on the DSC denaturation curve and shown in Table 14.
As a result, the Tm values of Fab domains of the antibodies containing hVk1, hVk2, hVk3 and hVk4 sequences, respectively, did not change even if the calcium-ion concentrations of the solutions containing the Fab domains changed. In contrast, the Tm value of the Fab domain of the antibody containing hVk5 sequence changed depending upon the calcium-ion concentration of the solution of the antibody containing the Fab domain. From this, it was demonstrated that the hVk5 sequence binds to a calcium ion.
hVk5 Sequence
In the Kabat database, an hVk5-2 sequence alone is registered as the hVk5 sequence. Hereinafter, hVk5 and hVk5-2 are regarded as being identical in the following description.
Construction, Expression and Purification of hVk5-2 Sequence without Addition of Sugar Chain
The hVk5-2 sequence has an N-linked sugar chain, which is added to the amino acid at 20-position (Kabat numbering). Since the sugar chain added to the protein is heterogeneous, it is desirable that a sugar chain is not added in view of homogeneity of a substance. Then, a modified hVk5-2_L65 (SEQ ID NO: 62) was prepared by substituting the Asn (N) residue at position 20 (Kabat numbering) by a Thr (T) residue. An amino acid was substituted in accordance with a method known to those skilled in the art using a QuikChange Site-Directed Mutagenesis Kit (Stratagene). DNA encoding modified hVk5-2_L65 was integrated into an animal expression vector. The animal expression vector was introduced into an animal cell together with an animal expression vector to which a heavy chain i.e., CIM_H (SEQ ID NO: 63) is integrated so as to express this sequence, in accordance with the method described in Reference Example 4. An antibody having hVk5-2_L65 and CIM_H expressed therein in the animal cell was purified by the method described in Reference Example 4.
Evaluation of Physical Properties of an Antibody Containing hVk5-2 Sequence without Addition of Sugar Chain
Whether the degree of heterogeneity of the obtained antibody containing the modification sequence hVk5-2_L65 is low or not compared to that of the antibody containing the original hVk5-2 sequence (subjected to modification) was analyzed by ion exchange chromatography. The details of ion exchange chromatography are shown in Table 15. As a result of the analysis, it was shown that the degree of heterogeneity of hVk5-2_L65 (modified at a glycosylation site) is low compared to that of the original hVk5-2 sequence, as shown in
Whether an antibody containing an hVk5-2_L65 sequence having a low degree of heterogeneity binds to a calcium ion or not was evaluated by the method described in Reference Example 6. As a result, as shown in Table 16, the Tm value of a Fab domain of an antibody containing hVk5-2_L65 having a modified glycosylation site varies depending upon a change of the calcium-ion concentration of an antibody solution. More specifically, it was shown that a calcium ion bind to the Fab domain of the antibody containing hVk5-2_L65 (having a modified glycosylation site).
Preparation, Expression and Purification of Modified Antibody Containing CDR Sequence of hVk5-2 Sequence
The hVk5-2_L65 sequence is a sequence in which an amino acid of a glycosylation site present in a framework of human Vk5-2 sequence is modified. Reference Example 12 shows that even if the glycosylation site is modified, a calcium ion can bind. In general, a framework sequence is desirably a genital cell lineage sequence in view of immunogenicity. Then, whether or not the framework sequence of the antibody can be converted to the framework sequence of a genital cell lineage sequence (to which a sugar chain cannot be added), while maintaining the binding activity of a calcium ion to the antibody, was investigated.
Polynucleotides encoding sequences, namely, CaVk1 (SEQ ID NO: 64), CaVk2 (SEQ ID NO: 65), CaVk3 (SEQ ID NO: 66), CaVk4 (SEQ ID NO: 67) (which were prepared by replacing the framework sequence of the hVk5-2 sequence chemically synthesized with hVk1, hVk2, hVk3 and hVk4 sequences, respectively), were each ligated to a polynucleotide encoding a constant region (SEQ ID NO: 42) of a natural Kappa chain by a PCR method to prepare a DNA fragment. These DNA fragments were each integrated into an animal cell expression vector. The sequence of the modified form prepared was determined by a method known to those skilled in the art. The plasmid prepared as mentioned above was introduced into an animal cell together with a plasmid, in which a polynucleotide encoding CIM_H (SEQ ID NO: 63) was integrated, in accordance with the method described in Reference Example 4. The animal cell was cultured and a desired antibody molecule was expressed. From the culture fluid, the desired antibody molecule was purified.
Evaluation of Calcium Ion-Binding Activity of Modified Antibody Containing CDR Sequence of hVk5-2 Sequence
Whether or not a calcium ion binds to a modified antibody, which contains a framework sequence of a genital cell lineage sequence (hVk1, hVk2, hVk3, hVk4) except an hVk5-2 sequence and a modified antibody containing a CDR sequence of the hVK5-2 sequence, was evaluated by the method described in Reference Example 6. The evaluation results are shown in Table 17. It was shown that the Tm value of the Fab domain of each modified antibody changes depending upon a change of the calcium-ion concentration of an antibody solution. Accordingly, it was demonstrated that antibodies having framework sequences other than the framework sequence of the hVk5-2 sequence can bind to a calcium ion.
It was further elucidated that the thermal denaturation temperature (Tm value, serving as an index of thermal stability of the F domain) of each of the antibodies modified (so as to contain framework sequences of genital cell lineage sequences (hVk1, hVk2, hVk3, hVk4) except an hVk5-2 sequence) and an antibody modified so as to contain a CDR sequence of an hVK5-2 sequence, is higher than the Tm value of the F domain of an antibody containing the original hVk5-2 sequence. From the result, it was found that the antibodies containing the framework sequences hVk1, hVk2, hVk3, and hVk4 and the antibody containing a CDR sequence of an hVk5-2 sequence have a property of binding to a calcium ion and are excellent molecules in view of thermal stability.
Designing of Mutation Site in CDR Sequence of hVk5-2 Sequence
As described in Reference Example 13, it was shown that an antibody containing a light chain, in which the CDR sequence of the hVk5-2 sequence is introduced into a framework sequence of a different genital cell lineage, can bind to a calcium ion. From the result, it was suggested that the calcium ion-binding site present within hVk5-2 is present in CDR. As an amino acid binding to a calcium ion, more specifically, chelating a calcium ion, an amino acid negatively charged or an amino acid that will serve as an acceptor for a hydrogen bond is mentioned. Then, whether or not an antibody containing a mutated hVk5-2 sequence (prepared by substituting an Asp (D) residue or a Glu (E) residue present in CDR sequence of the hVk5-2 sequence with an Ala (A) residue) binds to a calcium ion was evaluated.
Preparation of an Ala-Substituted hVk5-2 Sequence and Expression and Purification of Antibody
An antibody molecule containing a light chain, which has a modification of an Asp and/or a Glu residue (present in the CDR sequence of an hVk5-2 sequence) into an Ala residue, was prepared. As described in Reference Example 12, the modified hVk5-2_L65 form (to which no sugar chain is added) maintained a calcium ion-binding ability. From this, it is considered that the modified hVk5-2_L65 form is equivalent to the hVk5-2 sequence in calcium ion-binding ability. In this Reference Example, an amino acid was substituted by using the hVk5-2_L65 form as a template sequence. The modified antibodies prepared are shown in Table 18. Amino acid substitution was performed by use of a QuikChange Site-Directed Mutagenesis Kit (Stratagene), PCR or In fusion Advantage PCR cloning kit (TAKARA) etc., in accordance with a method known to those skilled in the art to construct an expression vector having a modified light chain having an amino acid substitution.
The nucleotide sequences of the obtained expression vectors were determined in accordance with a method known to those skilled in the art. The expression vector of a modified light chain was prepared and temporarily inserted together with an expression vector of heavy chain CIM_H (SEQ ID NO: 63) into a human fetus kidney cancer cell-derived HEK293H strain (Invitrogen) or FreeStyle 293 cell (Invitrogen) to express an antibody. From the obtained culture supernatant, the antibody was purified by use of rProtein A Sepharose Fast Flow (GE Healthcare) in accordance with a method known to those skilled in the art. Absorbance of the purified antibody solution was measured at 280 nm by a spectrophotometer. From the obtained measurement value, the concentration of the antibody was computationally obtained by use of an absorption constant calculated by a PACE method (Protein Science (1995) 4, 2411-2423).
Evaluation of Calcium Ion-Binding Activity of Antibody Having Ala Substitution in hVk5-2 Sequence
Whether the purified antibody obtained binds to a calcium ion or not was determined by the method described in Reference Example 16. The results are shown in Table 19. Even though an Asp or a Glu residue is substituted with an Ala residue (which cannot be involved in binding or chelating calcium ion) present in the CDR sequence of an hVk5-2 sequence, there was an antibody having a Fab domain whose Tm value does not change even if the calcium-ion concentration of an antibody solution changes. It was shown that the Ala substitution sites (position 32 and position 92 (Kabat numbering)), whose substitution does not change the Tm value, are particularly important for binding between a calcium ion and the antibody.
Preparation of hVk1 Sequence Having a Calcium Ion-Binding Motif and Expression and Purification of Antibody
From the results of the calcium binding activity of Ala substitution antibody described in Reference Example 14, it was shown that Asp and Glu residues in the CDR sequence of an hVk5-2 sequence are important for calcium binding. Then, only the residues of the position 30, position 31, position 32, position 50 and position 92 (Kabat numbering) were introduced into a variable region sequence of a different genital cell lineage, and then, whether the genital cell lineage can bind to a calcium ion or not was evaluated. To describe more specifically, the position 30, position 31, position 32, position 50 and position 92 (Kabat numbering) residues of the hVk1 sequence (human genital cell lineage sequence) were substituted with the position 30, position 31, position 32, position 50 and position 92 (Kabat numbering) of the hVk5-2 sequence to prepare a modified antibody LfVk1_Ca (SEQ ID NO: 76). More specifically, whether or not an antibody containing an hVk1 sequence to which there five residues alone of the hVk5-2 sequence were introduced can bind to calcium, was evaluated. The modified antibody was prepared in the same manner as in Reference Example 4. The obtained LfVk1_Ca having a light chain modification and LfVk1 (SEQ ID NO: 77) containing a light-chain hVk1 sequence were expressed together with heavy chain CIM_H (SEQ ID NO: 63). The antibodies were expressed and purified in the same manner as in Example 14.
Evaluation of Calcium Ion-Binding Activity of Antibody Having Human hVk1 Sequence Having a Calcium Ion-Binding Motif
Whether the purified antibodies obtained as mentioned above bind to a calcium ion or not was determined in the method described in Reference Example 6. The results are shown in Table 20. The Tm value of the Fab domain of the antibody containing LfVk1 having an hVk1 sequence does not change even if the calcium concentration of the antibody solution changes. In contrast, the Tm value of the antibody sequence containing LfVk1_Ca changes by 1° C. or more when the calcium concentration of the antibody solution changes. From this, it was demonstrated that an antibody containing LfVk1_Ca binds to calcium. From the above results, it was demonstrated that the entire hVk5-2 CDR sequence is not required, only the residues introduced in constructing the LfVk1_Ca sequence are sufficient in binding to a calcium ion.
Other than Vk5-2 (SEQ ID NO: 6), Vk5-2 variant 1 (SEQ ID NO: 78) and Vk5-2 variant 2 (SEQ ID NO: 79), which are classified into a Vk5-2 class, were obtained. These variants were evaluated for calcium binding. DNA fragments of Vk5-2, Vk5-2 variant 1 and Vk5-2 variant 2 were each integrated into an animal cell expression vector. The nucleotide sequences of the obtained expression vectors were determined in accordance with a method known to those skilled in the art. The animal cell expression vectors, in which the DNA fragments of Vk5-2, Vk5-2 variant 1 and Vk5-2 variant 2 were separately integrated were each introduced into an animal cell together with an animal expression vector in which a heavy chain, CIM_H (SEQ ID NO: 63) n was integrated such that the heavy chain can be expressed, by the method described in Reference Example 13 to produce an antibody. The obtained antibody was purified. The calcium ion-binding activity of the purified antibody was evaluated. The antibody purified was subjected to dialysis (EasySEP, TOMY) treatment using a solution containing 20 mM Tris-HCl, 150 mM NaCl, 2 mM CaCl2 (pH 7.5) or 20 mM Tris-HCl, 150 mM NaCl (pH 7.5) (calcium-ion concentration is described as 0 mM in Table 21) as an external solution. An antibody solution was prepared with the solution used in dialysis so as to obtain concentration of 0.1 mg/mL and then the antibody solution (a test subject) was subjected to DSC measurement by raising temperature from 20° C. to 115° C. at a rate of 240° C./hr. The thermal denaturation intermediate temperature (Tm value) of a Fab domain of each antibody obtained was calculated based on the DSC denaturation curve and shown in Table 21.
As a result, the Tm values of Fab domains containing Vk5-2, Vk5-2 variant 1 and Vk5-2 variant 2, respectively, changed depending upon the calcium-ion concentration of the antibody solution containing the respective Fab domains. From this, it was shown that an antibody having a sequence classified into Vk5-2 binds to a calcium ion. It is elucidated that the calcium-binding motifs present in the sequences of Vk5-2 variant 1 and Vk5-2 variant 2 can be preferably used as a calcium-binding motif changing the binding activity of an antigen-binding domain to an antigen depending upon the ion-concentration condition of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-221400 | Oct 2011 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2012/006453 | 10/5/2012 | WO | 00 |
