Patent Application
20140308281
The invention concerns antibodies directed against the alpha chain of the receptor for interleukin7 (IL-7), especially the receptor for human IL-7 expressed on human cells (also designated human IL-7Ralpha or IL-7Ra). The alpha chain of the receptor for interleukin7 (IL-7) is also designated CD127.
The antibodies of the invention have cytotoxic activity against CD127 positive cells.
The invention also relates to the use of these antibodies in order to deplete subpopulations of lymphocytes, or other cell populations expressing CD127 (including T lymphocytes, B lymphocytes, NK cells and dendritic cells) as a result of cytotoxic action of the antibodies, through ADCC (Antibody-Dependent Cellular Cytotoxicity) and optionally through CDC (Complement-Dependent Cytotoxicity). Accordingly the invention concerns the use of the antibodies in the treatment of pathologic conditions involving the alteration of immune response in a human patient leading to dominant tolerogenic state or, to the contrary, lack of tolerance where control of the level of the immune response would be needed as well as destruction of malignant CD127-positive cells. The invention thus provides means suitable for use in pathologies such as those induced by transplant rejection, autoimmune diseases, lymphoma or cancer when these pathologies are associated with CD127 positive cells.
Naive T cells are partly responsible for acute rejection of transplanted organs and tissues. These cells can be controlled by current immunosuppressive drugs (calcineurin inhibitors) and by monoclonal antibodies that block costimulation (anti-adhesion, CD80/86 inhibitors). Memory T cells are also responsible for transplant rejection. Memory T cells accumulate in man due to the acquired immune history, mainly former reactions against viruses. It has been shown that memory T cells can be reactivated by alloantigens as a result of “heterologous immunity”, which is the cross-reaction of our anti-viral defenses with alloantigens (Adams et al, Immunol Rev 2003, 196, 147-60). Heterologous immunity represents a potent barrier to tolerance induction since memory T cells, in contrast to naive T cells, are programmed to activate quickly, with a reduced requirement for costimulatory signals. Memory T cells may also be involved in chronic rejection. Beside their role in organ and tissue transplantation, naïve and memory T cells are also co-responsible for many autoimmune diseases. This is the case for ulcerative colitis (Shinohara et al, J. Immunol. 2011, 186: 2623-32), rheumatoid arthritis, psoriasis or graft-versus-host disease.
Furthermore, several malignant cells have been shown to display IL-7R. This is the case for Sezary cutaneous lymphoma (60% of them), or childhood acute lymphoblastic leukemia in which about 15% of the cases develop gain-of-function mutation in CD127, rendering these tumors partially IL-7 dependent (Shochat et al, J Exp Med. 2011 May 9; 208(5):901-8).
CD127 is expressed by various cells, including by both memory and naive T cells. CD127 is in particular expressed by effector T cells (Teff), including resting and memory T cells, and by immature B cells, but is especially not expressed by resting natural regulatory T cells (natural Treg). IL-7Ra is essential for promoting thymocyte differenciation and clonal expansion of lymphocytes.
The role of the IL-7/CD127 pathway in transplantation rejection has been suggested by the effect of an anti-IL-7 Mab which, when associated with costimulation blockade, prolonged heart allograft survival in mice (Wang et al, Am J Transplant 2006, 6 (12), 2851-60). The role of the IL-7/CD127 pathway in autoimmunity has also been suggested by the effect of a blocking anti-IL-7Ra Mab which prevented autoimmune experimental encephalomyelitis in mice (Liu et al, Nature Medicine 2010, 16 (2), 191-198).
The depletion of T lymphocytes has been an obvious immunosuppressive approach to counteract allograft rejection or fight autoimmunity. However, total T cell depletion might not be favorable for the induction of immunological tolerance. Targeting T cell subpopulations or selectively activated T cells, without modifying Treg cells, could constitute a pro-tolerogenic approach (Haudebourg et al Transpl Int 2009, 22 (5), 509-18). CD127 may thus be regarded as a potential attractive therapeutic target for monoclonal antibodies (Mabs) aimed at modulating immune responses since such monoclonal antibodies could have the potential of depleting effector but not regulatory lymphocytes. It has been assumed accordingly that they might show efficacy in transplantation, autoimmunity (Michel et al, J Clin Invest. 2008 October; 118(10):3411-9.) and malignancies by antagonizing access of IL-7 to IL7-R and thereby limiting T and B cell function and growth.
A therapy with a monoclonal antibody against CD127+ cells with cytotoxic activity could fulfill that goal by eliminating/neutralizing naïve and memory T cells while preserving Treg cells or eliminating CD127-positive malignant cells.
In this context, monoclonal antibodies against IL-7Ra having antagonist properties toward IL-7Ra have been disclosed in WO2010/017468, with a view to treat autoimmune diseases like multiple sclerosis. The described antibodies are said to be antagonist for IL-7 binding to its receptor, and active against TH17 and TH1 cells expansion and survival which were said to require IL-7 interaction with their CD127 receptor.
In a publication (Racapé M. et al, Arch. Immunol. Ther. Exp., 2009, 57, 253-261) the authors analysed the interest of IL-7 receptor alpha as a potential therapeutic target in transplantation. Having reviewed the expression of IL-7Ralpha on various T cells and IL-7 responsive cells, the authors determined whether targeting memory T cells expressing IL-7Ralpha could prolong allograft survival in mice and conclude that targeting IL-7 or IL-7Ralpha would advantageously spare Treg cells. Among the perspectives, the authors pointed out that targeting either IL-7 or IL-7Ralpha in therapeutic treatment might have different consequences on the survival of the cells expressing CD127 and might elicit different type of lymphopenia. The question of the effects of antibodies that would be directed against IL-7Ralpha depending upon whether they would be blocking or neutralizing or cytotoxic antibodies was also posed from a conceptual point of view. The authors nevertheless did not show having obtained and assayed such antibodies and rather expressed the need for further study to assess the relevancy of the hypothesis.
In view of the drawbacks of available therapeutic approaches in immune related diseases including transplant acute or chronic rejection, and other diseases involving the IL-7/IL-7Ralpha such as different types of cancers, including some breast cancers, there is still a need for further drug candidates, especially for candidates active with respect to more selective targets for the purpose of controlling e.g. modulating immune activation in human patients.
The inventors fulfil this need in providing antibodies that have the capacity to deplete aggressive effector cells while preserving pro-tolerogenic regulatory T cells, and that have shown ability to eliminate malignant cells in CD127+ lymphoma. More generally, the inventors provide antibodies that display a cytotoxic activity against human CD127+ cells especially human CD127+ T or B cells.
The inventors provide means suitable in this context, as they obtained monoclonal antibodies against IL-7Ra that also exert a cytotoxic action against target CD127+ cells and physically reduce their number (contraction of the subpopulation). In a particular embodiment, the inventors have also obtained such antibodies that combine this property with antagonist activity toward IL-7/IL7-R interaction. These Mabs with novel mechanisms of action therefore constitute new products for evaluating therapeutic benefits of CD127 targeting.
The invention thus concerns an antibody or a functional fragment thereof which binds the alpha chain of the receptor to IL-7 (designated CD127), especially of the alpha chain of the IL-7 receptor expressed by human CD127 positive cells, and which exhibits cytotoxic activity against human T cells expressing CD127 (CD127+ cells). in particular of the IL-7 receptor expressed by human T cells,
In a particular embodiment, the antibodies of the invention or their functional fragments are directed against the CD127 molecule present in the iL-7 receptor and are accordingly cytotoxic against human cells, especially human T cells expressing said receptor.
In a particular embodiment of the invention, the antibodies of functional fragments thereof target and bind the same IL7-R alpha chain when it is combined with TSLP-Receptor (also known as CCRF2; Accession Number AF338733; Reche P. A. et al J Immunol. 167(1), 336-343 (2001)) as a receptor for TSLP (Reche P. A. et al, 2001). Human TSLP (Accession number AF338732) is a factor which exerts polarization of dendritic cells, promote T and B cell proliferation and differentiation and which has been shown to play a role in skin and lung diseases (Rui et al, Ann N Y Acad. Sci. 2010, 1183: 13-24). Accordingly TSLP has been shown to associate to various pathologies including airway inflammatory disease and atopic dermatitis in human and mice (Ying S. et al (2008) J Immunol 181:2790-2798; Jariwala S P. Et al (2011) Clin Exp Allergy June 14). In addition TSLP has been shown to associate to regulation of intestinal immunity and inflammation (Taylor B C. Et al (2009) J Exp Med 206: 655-667).
A “functional fragment” of an antibody of the invention is a part of the antibody, i.e. a molecule corresponding to a portion of the structure of the antibody of the invention that exhibits antigen-binding capacity (also designated as an antigen-binding fragment) for alpha chain of the IL-7 receptor for human IL-7, possibly in its native form; such fragment especially exhibits the same or substantially the same antigen-binding capacity for said antigen compared to the antigen-binding capacity of the corresponding four-chain antibody. The antigen-binding capacity can be determined by measuring the affinity of the antibody and of the considered fragment.
Functional fragments of antibodies are fragments which comprise their hypervariable domains designated CDRs (Complementary Determining Regions) or part(s) thereof encompassing the recognition site for the antigen, i.e., IL-7Ra of human IL-7, thereby defining antigen recognition specificity. Each Light and Heavy chain (respectively VL and VH) of a four-chain immunoglobulin has three CDRs, designated VL-CDR1, VL-CDR2, VL-CDR3 and VH-CDR1, VH-CDR2, VH-CDR3, respectively.
Thus the invention relates to fragments of antibodies of the invention, which comprise or consist in all or a selection of CDRs among VL-CDR1, VL-CDR2, VL-CDR3 and VH-CDR1, VH-CDR2 and VH-CDR3 or functional portions thereof, i.e. portions that exhibit the desired binding capacity preferably with a high affinity for IL-7Ra of human IL-7.
Fragments that comprise or consist in VH-CDR3 and/or VL-CDR3 or functional portions thereof are especially preferred when CDR3 regions appear to be determinant in antigen recognition specificity.
The skilled person will be able to determine the location of the various regions/domains of antibodies by reference to the standard definitions in this respect set forth, including a reference numbering system [Martin, A. C. R. (2001) Protein Sequence and Structure Analysis of Antibody Variable Domains. In: Antibody Engineering Lab Manual, ed.: Duebel, S, and Kontermann, R., Springer-Verlag, Heidelberg] or by reference to the numbering system of Kabat (Sequences of Proteins of Immunological Interest, 4th Ed., U.S. Department of Health and Human Services, NIH, 1987) or by application of the IMGT “collier de perle” algorithm (http://www.imgt.org/IMGTindex/Colliers.html). In this respect, for the definition of the sequences of the invention, it is noted that the delimitation of the regions/domains may vary from one reference system to another. Accordingly, the regions/domains as defined in the present invention encompass sequences showing variations in length or localization of the concerned sequences within the full-length sequence of the variable domains of the antibodies, of approximately +/−10%.
Based on the structure of four-chain immunoglobulins, functional fragments can thus be defined by comparison with sequences of antibodies in the available databases and prior art (Martin A. C. R. et al), and especially by comparison of the location of the functional domains in these sequences, noting that the positions of the framework and constant domains are well defined for various classes of antibodies, especially for IgGs, in particular for mammalian IgGs.
For illustration purpose of specific embodiments of the invention, antigen-binding fragments of an antibody that contain the variable domains comprising the CDRs of said antibody encompass Fv, dsFv, scFv, Fab, Fab′, F(ab′)2 which are well defined with reference to Kabat (NIH 1987), Martin A. C. R. et al and also Roitt I. et al (Fundamental and Applied Immunology MEDSI/McGraw-Hill). Fv fragments consist of the VL and VH domains of an antibody associated together by hydrophobic interactions; in dsFv fragments, the VH:VL heterodimer is stabilised by a disulphide bond; in scFv fragments, the VL and VH domains are connected to one another via a flexible peptide linker thus forming a single-chain protein. Fab fragments are monomeric fragments obtainable by papain digestion of an antibody; they comprise the entire L chain, and a VH-CH1 fragment of the H chain, bound together through a disulfide bond. The F(ab′)2 fragment can be produced by pepsin digestion of an antibody below the hinge disulfide; it comprises two Fab′ fragments, and additionally a portion of the hinge region of the immunoglobulin molecule. The Fab′ fragments are obtainable from F(ab′)2 fragments by cutting a disulfide bond in the hinge region. F(ab′)2 fragments are divalent, i.e. they comprise two antigen-binding sites, like the native immunoglobulin molecule; on the other hand, Fv (a VH-VL dimmer constituting the variable part of Fab), dsFv, scFv, Fab, and Fab′ fragments are monovalent, i.e. they comprise a single antigen-binding site.
These basic antigen-binding fragments of the invention can be combined together to obtain multivalent antigen-binding fragments, such as diabodies, tribodies or tetrabodies. These multivalent antigen-binding fragments are also part of the present invention.
Human cells expressing CD127 as a chain of IL-7 receptor, which are the target of the antibodies of the invention and fragments thereof, are mainly T lymphocytes and more precisely are subpopulations of effector T lymphocytes including naïve and memory T cells but are not regulatory T cells, especially not resting natural Treg. Memory T cells are generated as a result of antigen priming and mainly defined by their functional characteristics, including ability to undergo recall proliferation upon re-activation and differentiation into secondary effector and memory cells. Similarly, the targeted TSLP receptor (as a combination structure with IL7-R alpha chain) masters the regulation of T helper lymphocytes, B cells and dendritic cells differentiation.
According to an embodiment of the invention, the antibodies having “cytotoxic activity against T cells” or cytotoxic properties (cytotoxic antibodies) give rise to depletion in the effector T cell population by killing these cells and accordingly reduce the number of these cells when administered. To the contrary, these antibodies do not alter the subpopulation of regulatory T cells or do not alter it to a significant extent, allowing the Treg cells to perform their function.
In this context, in a particular embodiment, it has been observed that the ratio of regulatory T (Treg) versus effector T (Teff) cells raises following administration of cytotoxic antibodies of the invention. In a particular embodiment, the cytotoxic antibodies of the invention enable to raise said ratio of about 10% or more. In a particular embodiment, the ratio of Treg versus Teff is of about 20%.
According to a particular embodiment of the invention, the cytotoxic antibodies show Antibody-Dependant Cellular Cytotoxicity (ADCC).
ADCC properties can be evaluated in an ADCC assay such as the test described in the Examples. When the antibody is a rat antibody the effector cells used in the ADCC assay are LAK (Lymphokine-activated killer) cells of rat. When the antibodies are humanized the ADCC assay can be carried out on human LAK cells.
According to a particular embodiment of the invention, the ADCC activity of the antibodies of the invention is achieved with a concentration of antibodies of at least 10 ng/ml. ADCC may be assayed with chimeric antibodies, i.e., with antibodies the constant fragment of which (Fc) is a human Fc fragment.
When an antibody harbors ADCC activity as a result of its binding to antigen, Fc fragment may help in observing this activity.
In this regard, the invention provides in particular MD707-3 antibodies or antibodies derived from MD707-3, in particular chimeric MD707-3 antibodies having a human Fc fragment having a level of ADCC activity of at least 80%, when assessed with target cells expressing recombinant human CD127.
According to another embodiment, a cytotoxic antibody or a functional fragment thereof within the frame of the invention further has antagonist properties toward interleukin 7 (IL-7) thereby antagonizing access, i.e. binding of IL-7 to CD127 on CD127 positive cells.
“Antagonist properties” mean that antibodies or functional fragments thereof of the invention, which target the IL-7Ralpha, have the effect of preventing the accessibility of the IL-7 receptor expressed on CD127 cells, especially human effector T cells, in particular human memory T cells, for its binding partner IL-7, especially human IL-7. As a result of antagonizing binding of IL-7, the antibodies of the invention or their functional fragments lead to lymphopenia by preventing I L-7-dependent thymic T cells generation. A test for measurement of the antagonist properties of the antibodies or functional fragments thereof of the invention is described in the Examples.
The antibodies of the invention which have both cytotoxic and antagonist properties for CD127 positive cells enable cumulative effects of these properties with respect to the depletion of effector T cells, especially of memory T cells especially, thereby enabling a stronger depletion (exhaustion of the pool of CD127+ cells) and corresponding reduction in the number of target T cells. According to another embodiment of the invention, the antibody or functional fragment thereof binds to the TSLP receptor through its IL-7R alpha chain. As a consequence, the antibody or the functional fragment of antibody of the invention performs TSLP inhibition as a result of modification of the T and B cells differentiation, especially impacting the so-called TH-2 differentiation observed in some autoimmune diseases and in asthma.
An antibody or a functional fragment thereof of the invention is in particular advantageously raised against a molecule which is the CD127 expressed by human T cells, possibly raised from an immunization under the form of native polypeptide or recombinant molecule
Immunization can be carried out according to the protocol disclosed in the Examples below: Recombinant CD127 Fc Chimera (10975-H03H Sino Biological, Beijing, China) was used to immunize rats such as rats of the LOU/C IgkIA strain available at the University of Louvain). Hybridoma were obtained by fusing spleen mononuclear cells with the LOU rat immunocytoma IR983F, a non-secreting and azaguanine resistant cell line, according to a previously described procedure (Chassoux et al, Immunology 1988 65 623-628). Hybridoma were first screened according to the capacity of the secreted monoclonal antibodies to bind to recombinant CD127 molecule (CD127 Fc Chimera; 10975-H03H, Sino Biological, Beijing, China). Hybridoma were then screened for the capacity of their monoclonal antibodies to bind to the CD127 expressed by human T cells.
According to a particular embodiment of the invention, a cytotoxic antibody or a functional fragment thereof is selected in the group of:
a) antibodies produced by hybridoma MD707-1 deposited at the CNCM under No I-4531 or functional fragments thereof, or;
b) antibodies expressed by recombinant eukaryotic cells which are recombined with nucleic acid molecule(s) identical to cDNA corresponding to RNA expressed in hybridoma MD707-1 deposited at the CNCM under No I-4531 that encodes an antibody of a) or a functional fragment thereof, and;
c) modified antibodies with respect to a) or b), having modified CDR regions in its Variable Heavy chain (VH) and/or in its Variable Light chain (VL), in particular keeping optionally at least one identical CDR3, CDR2 and/or CDR1 region in either of VH or VL or both, and/or having modified Framework (FR) and/or constant (CH) regions, said modified antibody having more than 70% identity, especially more than 75%, more than 80%, more then 85%, more than 90%, more than 95% or up to 99% identity over the whole length of its amino acid sequence, with the antibody of a) or b) or is a functional fragment thereof.
In another embodiment of the invention, the antibody or a functional fragment thereof is cytotoxic and antagonist with respect to IL-7 and is selected in the group of:
a) antibodies produced by hybridoma MD707-3 deposited at the CNCM under No I-4532 or hybridoma MD707-13 deposited at the CNCM under No I-4533 or functional fragments thereof, or;
b) antibodies expressed by recombinant eukaryotic cells which are recombined with nucleic acid molecule(s) identical to to cDNA corresponding to RNA expressed in hybridoma MD707-3 deposited at the CNCM under No I-4532 or hybridoma MD707-13 deposited at the CNCM under No I-4533 that encodes an antibody of a) or a functional fragment thereof, and;
c) modified antibodies with respect to a) or b), having modified CDR regions in its Variable Heavy chain (VH) and/or in its Variable Light chain (VL), in particular keeping optionally at least one identical CDR3, CDR2 and/or CDR1 region in either of VH or VL or both, and/or having modified Framework (FR) and/or constant (CH) regions, said modified antibody having more than 70% identity, especially more than 75%, more than 80%, more then 85%, more than 90%, more than 95% or up to 99% identity over the whole length of its amino acid sequence, with the antibody of a) or b) or is a functional fragment thereof The deposits of hybridoma under No I-4531, I-4532 and I-4533 were made on Sep. 28, 2011 at the CNCM (Collection Nationale de Cultures de Microorganismes, Paris, France) under the provisions of the Budapest Treaty.
“Hybridoma cells” according to the invention are cells generated from fusion of antibody producing cells (B Lymphocytes) from an animal previously immunized with a selected immunogen and fusion partner which are myeloma cells enabling to provide immortality to the resulting fusion cell. Myeloma cells and antibody producing cells (B cells such as splenocytes) can be of the same origin, and are eukaryotic cells in particular mammalian cells of the same animal. They can be alternatively of different origin, thus giving rise to an heterohybridoma. Myeloma cells such as the LOU rat immunocytoma IR983F, a non-secreting and azaguanine resistant cell line are chosen among cells that fail to produce immunoglobulins in order to enable the prepared hybridoma to secrete only monoclonal antibodies of the desired specificity. Other cells suitable for promoting ADCC such as those described in the following pages for the preparation of the antibodies through expression in recombinant cells may be used instead of the rat immunocytoma. Such cells are advantageously cells having a low or no fucosylation capacity.
Preparation of hybridoma suitable for carrying out the invention is performed according to conventional techniques. Embodiments are described in detail in the Examples of the present application of which the particular disclosed features can be adapted to other cells used as fusion partners.
Particular hybridoma of the invention, useful for the preparation of the antibodies or functional fragments thereof are MD707-1 deposited at the CNCM on Sep. 28, 2011 under No I-4531 or MD707-3 deposited at the CNCM on Sep. 28, 2011 under No I-4532 or MD707-13 deposited at the CNCM on Sep. 28, 2011 under No I-4533.
In view of the teaching provided by the present invention in relation to the properties of the monoclonal antibodies obtained from the deposited hybridoma, in order to express antibodies of the invention, the skilled person will be able to use alternative technologies such as expression libraries and expression systems, followed by selection of antibodies having the structure of those secreted by the hybridoma and having its binding and neutralisation properties. cDNA libraries can adequately be prepared from the RNA expressed in hybridoma of the invention and the appropriate sequences selected and expressed.
The functional fragments of the antibody may be obtained starting from the antibody, especially by using enzymatic digestion according to well known techniques including papain or pepsin digestion, or using any appropriate cleavage technique. They may be alternatively expressed in host cells modified by recombination with nucleic acid sequences encoding the amino acid sequence of said fragments, or may be synthesized, especially chemically synthesized.
Accordingly, the antibodies of the invention, including the modified antibodies, and the functional fragments of the antibodies can also be prepared by classical genetic engineering techniques, such as those described by Sambrook et al. [Molecular Cloning, A Laboratory Manual, 2nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989), and updated versions].
In accordance to the invention, “binding” to the IL-7Ra protein refers to an antigen-antibody type interaction and reference to “specific binding” properties of the antibodies or functional fragments thereof means that the antibodies or functional fragments thereof bind to the IL-7Ra protein and furthermore do not bind or bind with a significant weaker affinity to other proteins (eg common cytokine receptor γ-chain). Binding capacity can be assayed in accordance with the tests disclosed in the Examples and in particular can be assayed by ELISA, or Western Blot analysis.
In a particular embodiment, an antibody or a functional fragment thereof according to the invention comprises in its antigen-binding site at least one of the following polypeptides:
1) MD707-1
a) for the Variable Heavy chain:
b) for the Variable Light chain:
a) for the Variable Heavy chain:
b) for the Variable Light chain:
a) for the Variable Heavy chain:
b) for the Variable Light chain:
The invention also relates to the versions of the VH and VL polypeptides that encompass the signal peptide and correspond respectively to SEQ ID No 2, SEQ ID No 4, SEQ ID No 18, SEQ ID No 20, SEQ ID No 34 and SEQ ID No 36.
With a view to use the antibody of the invention or their functional fragments for administration to a human patient, it might be beneficial to derive humanized monoclonal antibodies or chimeric monoclonal antibodies and/or de-immunized antibodies, from antibodies of the invention which would be non-primate antibodies such as those illustrated in the Examples, especially to lower the immune reaction of the receiving host or patient against said antibodies. Functional fragments of these variant antibodies may be obtained also as humanized, chimeric or de-immunized variants.
An antibody or a functional fragment thereof, which is a humanized antibody is derived by substitution of amino acid residue(s) present in constant region(s) of the variable chain a non human antibody of the invention, i.e., in the framework regions of the VH and/or VL, for human amino acid residue(s) having corresponding location in human antibodies according to standard definition and numbering, wherein the substitution level is from 1% to 20%, in particular from 1% to 18% of the residues in said constant regions, i.e., framework. Said constant regions include FR regions defined in four-chain antibodies.
Particular examples of modified antibodies according to the invention encompass chimeric antibodies, humanized antibodies and/or a de-immunized antibodies.
A particular modified antibody has modified amino acid residues in the CDRs regions, said modification resulting in a de-immunisation by loss of the T cell epitopes in the variable domain of the non-human antibody. De-immunisation can be performed after determination of the T cell epitopes in the antibody variable domain, especially by in silico prediction, followed by point mutation in the sequence of the variable chains of the antibody that eliminates the functional T cell epitopes. In a preferred embodiment of the invention, the modification of the CDR(s) regions, especially of the CDR3 regions are limited to the extent necessary to de-immunisation with a view to administration to the human body, e.g. to decrease binding affinity of T cell receptors for HLA-classII/peptide complexes In a particular embodiment, the CDR3 region(s) of the VH and/or of the VL is (are) not modified. In another embodiment the FR regions and/or the CH regions are also modified, especially humanized.
Antibodies within the frame of the invention encompass accordingly an antibody based on the here above defined features, which is a humanized antibody especially one obtained by substitution of amino acid residue(s) present in constant region(s) of an antibody of the invention, for human amino acid residue(s) having corresponding location in human antibodies according to standard definition and numbering, wherein the substitution level is from 1% to 20% in particular from 1% to 18% of the residues in said framework regions, and where appropriate which is substituted for de-immunisation into some or all of the CDR(s) region(s). As mentioned above, the humanization primarily targets the Framework regions of the original antibodies. In some cases, humanization may alternatively or also concern CDR region(s) especially CDR1 and/or CDR2 region(s).
Humanization can hence be achieved considering the human germline Light chain or Heavy chain frameworks that show the highest sequence identity with the sequence of the non-human antibody or fragment, and selecting the amino acid residues, especially residues exposed at the surface in the antibody, to be substituted in said non-human antibody or fragment thereof, in order to conform to the corresponding human residue(s). In a particular embodiment some of or all the FRL and/or some of or all the FRH regions are fully human, i.e., are characteristic of human framework sequences. In another embodiment selected residues in some of all the FR regions are substituted.
Methods for humanizing antibodies are also well known in the art and are described for instance by Routledege et al. [“Reshaping antibodies for therapy”, in Protein Engineering of Antibody Molecules for Prophylactic and Therapeutic Applications in Man, 13-44, Academic Titles, Nottingham, England (1993)] or by Roguska et al. Protein Engineering, 9(10), 895-904, (1996)]. These methods can also apply to antigen-binding fragments, such as scFvs.
By way of example, the method known as “resurfacing” consists in replacing the set of surface residues in the frameworks of the variable region of a nonhuman antibody with a human set of surface residues, while the method known as CDR grafting consists of transferring the CDRs from a non-human antibody into the framework regions of a human antibody. CDR grafting is generally completed by framework optimization, consisting in the replacement of some residues of the human framework, in order to optimize the binding affinity.
The step of framework optimization has been recently simplified by the use of combinatorial libraries (Rosok. et al. J. Biol. Chem. 271, 22611-22618, 1996; Baca et al. J. Biol. Chem. 272, 10678-10684, 1997).
Another recent strategy available for antibody humanization preserves only the original nonhuman CDR3 sequences of light and heavy chain while the remaining sequence is selected from naive human V gene libraries (Rader et al, Proc. Natl. Acad. ScL U.S.A. 95, 8910-8915, 1998).
According to another embodiment of the invention, the antibodies are modified and are, as a result, chimeric antibodies, comprising domains or strand(s) of amino acid residues of different antibodies, in particular antibodies obtained from different animal species, combined together in a functional antibody.
The chimeric, humanized and/or de-immunized antibodies of the invention can belong to any class of immunoglobulins, like the non modified antibodies. Preferably, they belong to a subclass of the IgG class such as IgG1, IgG2, IgG3 or IgG4.
Methods for preparing recombinant antigen-binding fragments, or chimeric antibodies by combining the variable regions of an antibody with appropriate linkers, or with the constant regions of another antibody, are well known in the art.
The antibodies of the invention are said to be monoclonal antibodies, meaning that a composition of these antibodies is homogeneous, especially identical, in terms of antigen-binding specificity and accordingly in terms of variable region composition. Hence the antibodies may qualify as monoclonal even if they are obtained by techniques alternative to the technique of hybridoma.
According to another embodiment, the invention also relates to a chimeric molecule which comprises an antibody according to any of the definition provided herein or a functional fragment thereof, wherein said monoclonal antibody or functional fragment thereof is associated with a functionally different molecule. A chimeric molecule of the invention may be either a fusion chimeric protein or a conjugate resulting from any suitable form of attachment including covalent attachment, grafting, chemical bonding with a chemical or biological group or with a molecule, such as a PEG polymer or another protective group or molecule suitable for protection against proteases cleavage in vivo, for improvement of stability and/or half-life of the antibody or functional fragment. with similar techniques, especially by chemical coupling or grafting, a chimeric molecule can be prepared with a biologically active molecule said active molecule being for example chosen among toxins, in particular Pseudomonas exotoxin A (Risberg et al, PLoS One. 2011; 6(9):e24012), the A-chain of plant toxin ricin (Van Oosterhout et al, Int J. Pharm. 2001 Jun. 19; 221(1-2):175-86.) or saporin toxin (Flavell et al, Br J. Haematol. 2006 July; 134(2):157-70)), especially a therapeutic active ingredient, a vector (including especially a protein vector) suitable for targeting the antibody or functional fragment to specific cells or tissues of the human body, or it may be associated with a label or with a linker, especially when fragments of the antibody are used.
PEGylation of the antibody or functional fragments thereof is a particular interesting embodiment as it improves the delivery conditions of the active substance to the host, especially for a therapeutic application. PEGylation can be site specific to prevent interference with the recognition sites of the antibodies or functional fragments, and can be performed with high molecular weight PEG. PEGylation can be achieved through free Cysteine residues present in the sequence of the antibody or functional fragment or through added free Cysteine residues in the amino sequence of the antibody or functional fragment.
The invention concerns also a composition comprising antibodies or functional fragments thereof as defined herein, wherein the antibodies or functional fragments thereof are a homogeneous population of antibodies or functional fragments thereof or are monoclonal antibodies or functional fragments thereof.
The invention also concerns a composition or an assembly of compounds comprising antibodies as disclosed herein, or a chimeric molecule of the invention, which comprises:
a) antibodies having both cytotoxic activity against CD127 positive cells, especially CD127+ T cells and antagonist properties toward human IL-7 or,
b) a population of antibodies or functional fragments thereof having cytotoxic activity against CD127 positive cells, especially CD127+ T cells and a population of antibodies or functional fragments thereof having antagonist properties toward human IL-7, these populations of antibodies being either combined in a mixture or separated and, in this latter option, formulated for combined or sequential administration.
The definitions provided herein especially by reference to the antibodies of the invention, similarly apply to the functional fragments thereof except where it is technically obviously not relevant. These definitions also apply to molecules (in particular chimeric antibodies or chimeric molecules) or compositions comprising these antibodies or functional fragments thereof or derived from these antibodies, as disclosed in the present application. It is further specified that the functional fragments of the antibodies of the invention are derived from the antibodies from a conceptual or design point of view but may be prepared through various techniques, not necessarily having recourse to the antibodies as products.
The invention also relates to a nucleic acid molecule encoding an antibody according to any of the definitions provided herein. Such a nucleic acid suitable for the preparation of antibodies of the invention or functional fragments thereof is especially chosen in the group of:
1) MD707-1
2) MD707-3
3) MD707-13
According to a particular embodiment of the invention, polynucleotides have modified nucleotides with respect to the sequence of SEQ ID No 1, SEQ ID No 3, SEQ ID No 5, SEQ ID No 7, SEQ ID No 9, SEQ ID No 11, SEQ ID No 13, SEQ ID No 15, SEQ ID No 17, SEQ ID No 19, SEQ ID No 21, SEQ ID No 23, SEQ ID No 25, SEQ ID No 27, SEQ ID No 29, SEQ ID No 31, SEQ ID No 33, SEQ ID No 35, SEQ ID No 37, SEQ ID No 39, SEQ ID No 41, SEQ ID No 43, SEQ ID No 45, and/or SEQ ID No 47 and,
a) either encode a polypeptide having amino acid sequence of respectively SEQ ID No 2 or its fragment from position 19 to position 141, SEQ ID No 4 or its fragment from position 21 to position 133, SEQ ID No 6, SEQ ID No 8, SEQ ID No 10, SEQ ID No 12, SEQ ID No 14, SEQ ID No 16, SEQ ID No 18 or its fragment from position 19 to position 141, SEQ ID No 20 or its fragment from position 21 to position 133, SEQ ID No 22, SEQ ID No 24, SEQ ID No 26, SEQ ID No 28, SEQ ID No 30, SEQ ID No 32, SEQ ID No 34 or its fragment from position 22 to position 135, SEQ ID No 36 or its fragment from position 22 to position 129, SEQ ID No 38, SEQ ID No 40, SEQ ID No 42, SEQ ID No 44, SEQ ID No 46, and/or SEQ ID No 48 and/or
b) have at least 85%, preferably at least 90%, more preferably at least 95%, and most preferably at least 98% or at least 99% identity over their whole length with one of the polynucleotides having sequence of SEQ ID No 1 or its fragment from position 55 to position 423, SEQ ID No 3 or its fragment from position 61 to position 399, SEQ ID No 5, SEQ ID No 7, SEQ ID No 9, SEQ ID No 11, SEQ ID No 13, SEQ ID No 15, SEQ ID No 17 or its fragment from position 55 to position 423, SEQ ID No 19 or its fragment from position 61 to position 399, SEQ ID No 21, SEQ ID No 23, SEQ ID No 25, SEQ ID No 27, SEQ ID No 29, SEQ ID No 31, SEQ ID No 33 or its fragment from position 64 to position 405, SEQ ID No 35 or its fragment from position 67 to position 387, SEQ ID No 37, SEQ ID No 39, SEQ ID No 41, SEQ ID No 43, SEQ ID No 45, and/or SEQ ID No 47.
Another polynucleotide of the invention is a fragment of the polynucleotide having sequence of SEQ ID No 1, SEQ ID No 3, SEQ ID No 5, SEQ ID No 7, SEQ ID No 9, SEQ ID No 11, SEQ ID No 13, SEQ ID No 15, SEQ ID No 17, SEQ ID No 19, SEQ ID No 21, SEQ ID No 23, SEQ ID No 25, SEQ ID No 27, SEQ ID No 29, SEQ ID No 31, SEQ ID No 33, SEQ ID No 35, SEQ ID No 37, SEQ ID No 39, SEQ ID No 41, SEQ ID No 43, SEQ ID No 45, and/or SEQ ID No 47 and encodes a functional fragment of a polypeptide having amino acid sequence of respectively SEQ ID No 2, SEQ ID No 4, SEQ ID No 6, SEQ ID No 8, SEQ ID No 10, SEQ ID No 12, SEQ ID No 14, SEQ ID No 16, SEQ ID No 18, SEQ ID No 20, SEQ ID No 22, SEQ ID No 24, SEQ ID No 26, SEQ ID No 28, SEQ ID No 30, SEQ ID No 32, SEQ ID No 34, SEQ ID No 36, SEQ ID No 38, SEQ ID No 40, SEQ ID No 42, SEQ ID No 44, SEQ ID No 46, and/or SEQ ID No 48.
Polynucleotides of the invention can be optimized sequences, especially for the expression in host cells. Optimisation techniques in this field are conventional one.
For the purpose of recovery of the antibodies of the invention from producing cells the polynucleotide may comprise, upstream from the nucleotide sequence encoding the antibody chains, a sequence encoding a signal peptide for secretion of the expressed antibody.
Polynucleotide fragment above have advantageously a sequence of at least 9 nucleotides and are shorter than their sequence of origin.
According to a particular embodiment, polynucleotides of the invention may advantageously comprise, besides a sequence encoding an antibody or a functional fragment thereof according to the invention, or a chimeric molecule including the same as disclosed herein, a sequence encoding a signal peptide allowing secretion of said protein when expressed in a production cell. They may also comprise one or more sequence(s) encoding one or more marker peptide(s) for detecting, and/or facilitating the purification of, said protein.
The invention also concerns a vector for the cloning and/or for the expression of a polynucleotide disclosed herein, and is especially a plasmid suitable for cloning and/or expressing in mammalian cells, which comprises regulation sequences for transcription and expression.
The invention further relates to cells or cell lines recombined with a polynucleotide of the invention, especially a mammalian or an avian cell or cell line. For example Chinese Hamster Ovary Cells, genetically modified to reduce global fucosylation. Indeed, Antibodies lacking core fucosylation show a significantly enhanced antibody-dependent cell-mediated cytotoxicity (ADCC) (von Horsten et al, Glycobiology. 2010 December; 20(12):1607-18). Another example is the EB66 cell line which naturally has low fucosylation properties (Olivier et al, MAbs. 2010 Jul. 16; 2(4)).
Thus the invention also relates to a method of preparing an antibody or a functional fragment thereof, which comprises:
Another object of the invention is a pharmaceutical composition comprising an antibody or a functional fragment thereof or a chimeric molecule, according to the invention, with a pharmaceutical vehicle, wherein said pharmaceutical composition optionally further comprises a different active ingredient.
The invention also relates to a composition comprising as an active ingredient, an antibody or a functional fragment thereof or a chimeric molecule according to the definitions provided herein or a pharmaceutical composition, in a formulation suitable for controlling human CD127 positive cells survival or expansion, in particular human CD127 positive effector cells, especially CD127+ memory T cells survival or expansion, especially memory T cells which are both CD127+ and CD8+, or which are both CD127+ and CD4+ cells, when administered to a human patient.
A composition of the invention may further comprise an additional compound having a therapeutic immunomodulator effect, in particular on cells involved in allergy or autoimmunity. For illustration purpose immunomodulators of interest are other monoclonal antibodies targeting T cells, such as anti-CD3, anti-ICOS or anti-CD28 antibodies or recombinant proteins or antibodies targeting accessory cells such as CTLA4Ig or anti-CD40 antibodies.
The invention concerns also an antibody or a functional fragment thereof or a chimeric molecule as defined or illustrated herein, for use as active ingredient in a combination or add-on therapeutic regimen in a patient in need thereof.
An antibody or a functional fragment thereof or a chimeric molecule according to the invention, a pharmaceutical composition or a composition as defined herein are in particular proposed for use in a human patient for treating pathologic conditions influenced by immune responses, especially by memory T cells responses. Accordingly, the inventors proposed that the antibody or functional fragment thereof, chimeric molecule according to the invention, pharmaceutical composition or composition as defined herein be used for preventing organ or tissue transplant rejection or for the treatment of autoimmune or allergic diseases or a for the treatment of a cancer such as breast cancer associated with CD127+ cells, or for the treatment of a T cell cutaneous lymphoma, such as Sezary lymphoma, or for the treatment of the acute lymphoblastoid leukemia with gain-mutation of the IL7-R/TSLP pathway. By interacting with TSPLR the antibodies or functional fragments of the invention can also inhibit allergic reaction such as asthma.
By “treatment” or “therapeutic treatment”, it is meant that the performed steps of administration result in improving the clinical condition of an animal or a human patient in need thereof, who suffers from disorder(s) associated with the IL-7 pathway, i.e; involving the activation or proliferation of CD127 positive cells. Such treatment aims at improving the clinical status of the animal or human patient, by eliminating or lowering the symptoms associated with the disorder(s) related to the IL-7 or TSLP. pathway, i.e; involving the activation or proliferation of CD127 positive cells and/or in a preferred embodiment, restoring to health.
Additional features and properties of the invention will be apparent from the Examples and figures which follow.
Selective depletion of naïve and memory T cells with MD707.
ELISA profile of rat anti-human CD127 antibodies on plate coated with recombinant human IL-7 receptor at 5 μg/ml.
Cross-reactivity of rat anti-human CD127 antibodies analyzed by flow cytometry on human peripheral blood mononuclear cells (PBMCs), baboon PBMCs, macaque PBMCs and rat spleen cells. MFI: Median Fluorescence Intensity. The coordinates on the abissa are 101, 102, 103, 104, 105.
Antibody-dependent cellular cytotoxicity (ADCC) of rat anti-human CD127 antibodies after 4 h incubation with rat lymphokine-activated killer (LAK) cells as effector (E) cells and 51Cr-labled human T lymphocytes as target (T) cells at different ratio: E:T=30:1 (square), E:T=10:1 (triangle), E:T=3:1 (round) and E:T=1:1 (diamond). Percentage of specific cytotoxicity was determined by 51Cr release.
Inhibition of IL-7-induced proliferation by rat anti-human CD127 antibodies. Human T lymphocytes were incubated with antibodies for 3 days on OKT3-coated plate (1 μg/ml) and soluble recombinant human IL-7 protein (rhIL-7; Sino Biologicals, Beijing, China; reference 10975-H08H) at 100 UI/ml (square), 50 UI/ml (round) or 10 UI/ml (triangle). Proliferation was determined during the last 8 hours of incubation by incorporation of 3H-thymidine (1 μCi/wells). Proliferation of human T cells incubated in the absence of anti-CD127 antibodies on OKT3-coated plate with rhIL-7 was about 105 counts per minutes (cpm).
Amino acids and nucleotide sequences of VH and VL variable domains of MD707-1 (A), MD707-3 (B) and MD707-13 (C). The nucleic acid sequence encoding the signal peptide in each variable fragment is underlined. The amino acid sequences of respectively CDR1, CDR2 and CDR3 domains in each of the VH and VL for MD707-1, MD707-3 and MD707-13 are underlined, in accordance with the sequences disclosed as SEQ IDs. The nucleic acid sequences encoding these CDR sequences are therefore located in line with the underlined amino acid sequences in the figure.
8 week-old male Balb/c mice received either anti-IL-7Ra mAb (clone A7R34) 400 μg IP every other day for 21 days (n=5) or isotype control at the same schedule (n=5). Mice were sacrificed at day 21; blood and spleen were harvested for absolute T lymphocyte counting by conventional microscopy with a Malassez device.
8 week-old male Balb/c mice received either anti-IL-7Rα mAb (clone A7R34) 400 μg IP every other day for 21 days (n=5) or isotype control at the same schedule (n=5). Mice were sacrificed at day 21; mesenteric lymph nodes, and spleen were harvested for lymphocyte phenotyping by flow cytometry. Anti-IL-7Rα-treated mice had significantly higher CD3+CD4+CD25+FOXP3+ regulatory T cell frequency than control mice either in the lymph nodes (21.4 vs 12.5%) or in the spleen (20.3 vs 11.6% of CD4+ T cells) (p<0.01).
7 to 9 week-old male Balb/c mice (H-2b) were rendered diabetic by streptozotocin 250 mg/kg IP 5-10 days before graft. Each recipient received about 500 islets isolated from 7 to 9 week-old male C57BL/6 mice (H-2d). Control group received no treatment; treated group received anti-IL-7Rα monoclonal antibody (clone A7R34) 400 μg IP every other day started from 21 days before graft and continued to post-transplant day 90. Control mice had median graft survival of 21 days (range: 14-34 days) whereas 5 of 6 treated mice had indefinite graft survival (>160 days) (p=0.0002, log-rank test).
Female non-obese diabetic (NOD) mice 6 weeks of age were purchased from Charles-River France and maintained in our animal facilities. Blood glucose were measured every week from 10 weeks of age. Treatment group received anti-IL-7Rα monoclonal antibody (clone A7R34) 400 μg IP 3 times per week for 8 wks from week 8 to week 16 of age. Control group received PBS at the same volume and same schedule. At 52 weeks of age, ⅝ (62.5%) of control mice develop diabetes, whereas ⅛ treated mice has diabetes (p=0.028, log-rank test).
Antibody-dependent cellular cytotoxicity (ADCC) of chimeric clone 3 anti-human CD127 antibody on mouse BA/F3 cell line transfected with human CD127. Human NK cells used as effector (E) were incubated for 4 hours with 51Cr-labled mouse BA/F3 CD127-transfected cells as target (T) cells at different ratio: E:T=3:1 (round), 10:1 (triangle) or 30:1 (square) and different concentration of chimeric MD707-3. Percentage of specific cytotoxicity was determined by 51Cr release.
Antibody-dependent cellular cytotoxicity (ADCC) of chimeric clone 3 anti-human CD127 antibody on human T-cell acute lymphoblastic leukemia (T-ALL) cell lines. Human NK cells used as effector (E) were incubated for 4 hours with two different 51Cr-labled T-ALL cell lines as target (T) cells at different ratio: E:T=1:1 (round), 3:1 (triangle) or 10:1 (square) and different concentration of chimeric MD707-3. Percentage of specific cytotoxicity was determined by 51Cr release. A/Target cells were the DND41 T-ALL cell line which over-express CD127, B/Target cells were the Jurkat T-ALL cell line which express low level of CD127.
1. Preparation and Selection of Novel Anti-Human CD127 Mabs
Rats were immunized with recombinant hCD127-Ig (hCD127 fused with a constant fragment of an immunoglobulin—Sino Biologicals, Beijing, China; reference 10975-H03H) and monoclonal antibodies were derived according to conventional techniques. The immunization protocol used was as follows: recombinant CD127 Fc Chimera (10975-H03H Sino Biological, Beijing, China) was used to immunize rats of the LOU/C IgkIA strain. Fifty micrograms of proteins were suspended in Complete Freund Adjuvant and administered s.c. After 20 days, a recall injection of the protein suspended in Incomplete Freund Adjuvant was performed. Another similar recall injection was performed on days 60 and a boost injection was performed on day 90 with 100 micrograms proteins, 4 days before spleen cells collection.
Hybridoma were obtained by fusing spleen mononuclear cells with the LOU rat immunocytoma IR983F, a non-secreting and azaguanine resistant cell line, according to a previously described procedure (Chassoux et al, Immunology 1988 65 623-628). Hybridoma were first screened according to the capacity of the secreted monoclonal antibodies to bind to recombinant CD127 molecule (CD127 Fc Chimera; 10975-H03H, Sino Biological, Beijing, China). Hybridoma were then screened for the capacity of their monoclonal antibodies to bind to the CD127 expressed by human T cells.
Thirteen clones were first selected based on the recognition by secreted antibodies of recombinant CD127 (Sino Biologicals) among which 9 were further selected on the recognition of CD127 expressed by human T cells
Antibodies were produced and their isotype were characterized as well as their affinities by Surface Plasmon Resonance measurement using BIAcore technology (Table 1).
rCD127 Recognition of Anti-h-CD127 Mabs Assessed by ELISA
Recombinant hCD127 (Sino Biologicals, Beijing, China; reference 10975-H08H) was immobilized on plastic and increasing doses of Mabs were added to measure binding. After incubation and washing, peroxidase-labeled anti-rat immunoglobulin antibodies were added and revealed by conventional methods. Results revealed a better binding of MD707-1, 2, 3, 4, 9, 13, an intermediate binding of MD707-5 and 12, and a weak binding of MD707-6
Cross Reactivity of Anti-Human CD127 Mabs with Non-Human Primates
Mabs shown in table 1 were used in flow cytometry assays to study binding on primate T cells in comparison with human T cells. Rat T cells were used as a negative control, since it is unexpected that Mabs of rat origin recognize rat molecules. The data (
Antibody-Dependent Cellular Cytotoxicity (ADCC) of Anti-Human CD127 Mabs
ADCC refers to as the binding of an antibody to an epitope expressed on target cells and the subsequent Fc-dependent recruitment of effector immune cells expressing Fc receptors (essentially NK cells and activated lymphocytes), resulting in the killing of target cells mainly by granzyme/perforin-based mechanisms Mabs shown in table 1 were used in ADCC assays. Lymphokine activated killer cells (LAK) of rat origin (because the Mab was obtained from rat splenocytes) were used as effector cells to kill target human T cells expressing CD127, in the presence of Mabs. The data shown in
Antagonistic Properties of Anti-Human CD127 Mabs
The ability of a given Mab directed to a receptor to antagonize binding of a ligand to that receptor probably depends on the ability of that Mab to target an epitope that is used by the ligand for docking into the receptor. It might also depend on the ability of the Mab to modify target conformation and thereby modify the binding properties of the receptor. The data shown in
Nucleotides and Aminoacid Sequences of Anti-Human CD127 Mabs
VH and VL regions of the MD707 clones were sequenced using the RACE PCR technology. Briefly, total RNA was extracted, reverse transcribed and the resulting cDNA was poly-adenylated at the 3′ end of the molecules using dATP and the terminal transferase enzyme. A first 35-cycle PCR reaction was performed using a oligo dT anchor primer and Herculease enzyme (Stratagene). A second 35-cycle PCR was performed using nested PCR anchor primers. The resulting PCR product was then TA-cloned in E. Coli and after selection on ampicillin, resulting colonies were screened by restriction enzyme profiling and inserted cDNA sequenced. Nucleotidic sequences and deduced amino acid sequences are shown on
2. Activity of Surrogate Anti-CD127 Monoclonal Antibodies in Depletion of T cells
Surrogate Anti-Human CD127 Mabs Deplete Teff Cells and Increase Treg/Teff Ratios
To illustrate how anti-CD127 Mab do impact T cells, 9 week-old male Balb/c mice (H-2b) received anti-CD127 Mabs (clone A7R34 directed against mouse CD127), 400 μg IP every other day during 21 days. It was observed that T cells, as a result, were depleted in blood and in the spleen (
Surrogate Anti-Human CD127 Mabs Prevent Pancreatic Islet Graft Rejection
To understand how anti-CD127 Mabs might modulate allograft rejection, 7 to 9 week-old male Balb/c mice (H-2b) were rendered diabetic by streptozotocin 250 mg/kg IP 5-10 days before implantation of pancreatic ilets from C57BL/6 mice (H-2d). It was observed that control mice had median graft survival of 21 days (range: 14-34 days) whereas 5 of 6 treated mice had indefinite graft survival (>160 days) (p=0.0002, log-rank test;
Surrogate Anti-Human CD127 Mabs Prevent and Cure Diabetes in NOD Mice
To understand how anti-CD127 Mabs might modulate an autoimmune disease, female non-obese diabetic (NOD) mice of 6 weeks of age were treated with an anti-IL-7R monoclonal antibody (clone A7R34) 400 μg IP 3 times per week for 8 wks from week 8 to week 16 of age. Control group received PBS at the same volume and same schedule. Results, shown on
A chimeric antibody prepared with MD707-3 anti-CD127 Mab was obtained by substituting the Fc fragment of the original rat antibody, by a human Fc fragment.
For this chimeric antibody, the effector cells were fresh primary human NK cells isolated from peripheral blood mononuclear cells by negative selection using magnetic beads (NK isolation kit, Miltenyi Biotec, Bergisch Gladbach, Germany) using an AutoMACS cell sorting instrument. NK cells were incubated over-night at 37° C., 5% CO2, in RPMI 1640 Medium (Life Technologies, Carlsbad, Calif.) complemented with 10% FBS (Life Technologies), 100 IU/ml penicillin (Life Technologies), 0.1 mg/ml streptomycin (Life Technologies), 2 mM L-glutamine (Life Technologies) and 150 IU/ml of human IL-2 (Roche, Basel, Switzerland).
The target cells were labeled with 100 μCi (3.7 MBq) of 51Cr (PerkinElmer) for 1 h at 37° C. and washed three times with culture medium. Target cells were incubated with diluted antibodies or with excipient (culture medium) for 15 min at room temperature and 10 000 cells were placed in a 96-well U-bottom plate. Effector T cells were added at the indicated E:T (effector:target) cell ratio (final volume: 200 μl) for a 4 or 18 hours incubation period at 37° C. A total of 25 μl of the supernatant was then harvested and counted in a gamma counter (Packard Instrument).
The results of the assays are disclosed on
| Number | Date | Country | Kind |
|---|---|---|---|
| 11306353.1 | Oct 2011 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2012/069670 | 10/4/2012 | WO | 00 | 4/18/2014 |
