Patent Application
20230203108
The present invention relates to granzyme B variants with increased protease activities and/or increased resistance against inhibitors; polynucleotides encoding the granzyme B variants; cells expressing the granzyme B variants; pharmaceutical compositions comprising cells expressing the granzyme B variants; and pharmaceutical compositions comprising the granzyme B variants.
Granzymes are proteases including a group of family members. Granzymes are expressed in T cells and NK cells—cytotoxic lymphocytes—and when these cells recognize a target antigen, granzymes are secreted to target cells (cells expressing the target antigen) together with perforin and such to exert cytotoxic activity. After transferring into the target cells, granzymes cleave various substrates such as BID and caspases and finally activate signal transduction systems that are involved in apoptosis in the target cells, thereby inducing cell death of the target cells (NPL 1).
Of the granzyme family, granzyme A and granzyme B have been suggested to make a particularly large contribution to cytotoxic activity. While granzyme A functions by forming a dimer, granzyme B functions as a monomer. Thus, it is easy to produce, express, and purify variants of granzyme B using protein engineering, and research and development has been performed with a view to drug discovery. For example, various variants including granzyme B with an scFv that binds to a tumor-associated antigen fused thereto are reported (NPL 2).
On the other hand, there is a limit to the use of granzyme B as an anti-tumor agent. The reasons for this include the limited protease activity of natural granzyme B and suppression of granzyme B activity by the development of inhibitors to granzyme B in target cells. NPL 3 shows that PI-9, an inhibitor of granzyme B activity, is highly expressed in tumors. Moreover, NPL 4 shows that heparin, whose production is known to be enhanced in tumors, inhibits granzyme B activity. That is, in tumors in which these inhibitors are highly expressed, it is considered that granzyme B, even if it is allowed to act on such tumors, may not exert sufficient cytotoxic activity and thus has only limited antitumor activity.
As granzyme variants that have resistance to these inhibitors, PI-9-resistant (PTL 1 and NPL 5) and heparin-resistant (NPL 6) granzyme B variants have been reported in previous studies. Furthermore, there is a report of granzyme B variants (PTL 2) in which comprehensive alterations were made to rat granzyme B to cleave VEGF and VEGF receptors.
On the other hand, when cytotoxic substances such as granzymes are used for therapy, it is preferable that they exert cytotoxic effects specifically on target cells (e.g., tumor cells). As an example of techniques for achieving this, there is a report on a method that uses transgenic cells that are transfected with a gene encoding a wild-type granzyme or the like and a gene encoding a chimeric antigen receptor (CAR) such that the cells are activated by the binding of the CAR to a target antigen and come to express the granzyme or the like at an increased level (PTL 3).
The granzyme B variants reported in PTL 1 show minor enhancement of protease activity compared to human wild-type granzyme B, and may not have sufficient cytotoxic activity. In PTL 2, while comprehensive alterations were made to rat granzyme B, there is no disclosure of data on resistance to inhibitors, and it is unclear whether these variants exert sufficient cytotoxic activity in the presence of inhibitors.
Furthermore, previous studies have proposed methods of using purified granzyme B or its variants by direct intravenous injection and so on. In such methods of use, however, there is a risk that cells which have taken up the administered granzyme B may undergo cell death and cause serious side effects. Accordingly, there is also a need to study a technique other than direct injection, as a therapeutic method using granzyme B.
Based on the above problems, the present inventors aimed to increase the activity of granzyme B, by discovering multiple alterations that increase protease activity through comprehensive alterations and by combining the alterations. As a result, the present inventors found that the activity of granzyme B protease is enhanced by genetic alterations that have not been reported in prior literatures. Furthermore, the present inventors showed that combining those alterations can significantly increase the activity relative to that of wild-type granzyme B. Moreover, the present inventors examined the resistance of the variants to granzyme B inhibitors to show that the variants exhibit high protease activity even in the presence of such inhibitors.
Thus, the present disclosure provides granzyme B variants whose protease activity and/or resistance to inhibitors has been enhanced by genetic alterations, and further provides, as medical uses of the granzyme B variants, pharmaceutical compositions comprising such a variant, pharmaceutical compositions comprising a cell expressing such a variant, and pharmaceutical compositions comprising such a variant used in combination with a receptor and/or a therapeutic antibody.
The present disclosure is based on the above findings, and specifically encompasses the embodiments exemplarily described below.
[1] A granzyme B variant comprising one or more amino acid residues selected from 1) to 20) below:
1) T, E, N, or V at position 43; 2) L or F at position 44; 3) Q, L, or A at position 45; 4) I, E, F, or Q at position 46; 5) V at position 47; 6) F or K at position 48; 7) L at position 99; 8) A at position 106; 9) M at position 149; 10) L at position 151; 11) P at position 155; 12) L at position 172; 13) Q, E, or I at position 175; 14) P at position 183; 15) L at position 184; 16) R at position 200; 17) I at position 217; 18) F at position 219; 19) G or S at position 222; and 20) V at position 229.
[2] The granzyme B variant of [1], wherein the variant comprises any one of the combinations of amino acid residues 1) to 12) below:
1) L at position 44, K at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
2) L at position 44, E at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
3) F at position 44, K at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
4) F at position 44, E at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
5) L at position 44, I at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
6) L at position 44, E at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
7) L at position 44, F at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
8) L at position 44, Q at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
9) F at position 44, I at position 46, P at position 155, L at position 172, I at position 175 and R at position 200;
10) F at position 44, E at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
11) F at position 44, F at position 46, P at position 155, L at position 172, I at position 175, and R at position 200; and
12) F at position 44, Q at position 46, P at position 155, L at position 172, I at position 175, and R at position 200.
[3] The granzyme B variant of [1] or [2], wherein protease activity is enhanced more than that of human wild-type granzyme B.
[4] The granzyme B variant of any one of [1] to [3], which has resistance to an inhibitor to human wild-type granzyme B.
[5] The granzyme B variant of [4], wherein the inhibitor is PI-9 or heparin.
[6] An isolated nucleic acid encoding the granzyme B variant of any one of [1] to [5].
[7] A vector comprising the isolated nucleic acid of [6].
[8] A cell transformed or transduced with the isolated nucleic acid of [6] or the vector of [7].
[9] A cell expressing the granzyme B variant of any one of [1] to [5].
[10] A pharmaceutical composition comprising the isolated nucleic acid of [6], the vector of [7], or the cell of [8] or [9].
[11] A pharmaceutical composition comprising the granzyme B variant of any one of [1] to [5].
[12] A pharmaceutical composition for use in combination with administration of a cell expressing a receptor, wherein the composition comprises a granzyme B variant or a cell expressing a granzyme B variant,
wherein the receptor activates the cell expressing the receptor by its binding to a ligand, and
wherein the granzyme B variant has enhanced protease activity more than that of human wild-type granzyme B and has resistance to an inhibitor to human wild-type granzyme B.
[13] The pharmaceutical composition of [12], wherein the receptor is a chimeric receptor which comprises an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain, and binds to the ligand via the extracellular binding domain.
[14] The pharmaceutical composition of [12], wherein the receptor is a T-cell receptor whose ligand is a neoantigen.
[15] The pharmaceutical composition of any one of [12] to [14], wherein the granzyme B variant is the granzyme B variant of [1], [2], or [5].
[16] The pharmaceutical composition of any one of [12] to [15], which comprises the cell expressing the receptor.
[17] The pharmaceutical composition of [16], wherein the receptor and the granzyme B variant are expressed in the same T cell.
[18] A pharmaceutical composition for use in combination with administration of an antigen-binding molecule and administration of a cell expressing a chimeric receptor, wherein the composition comprises a granzyme B variant or a cell expressing a granzyme B variant,
wherein the antigen-binding molecule has an ability to bind to a target antigen,
wherein the chimeric receptor comprises an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain and is capable of binding to a cell expressing the target antigen via the binding of the extracellular binding domain to the antigen-binding molecule, and
wherein the granzyme B variant has enhanced protease activity more than that of human wild-type granzyme B and has resistance to an inhibitor to human wild-type granzyme B.
[19] The pharmaceutical composition of [18],
wherein the antigen-binding molecule comprises a linker that is cleavable by a protease, and
wherein the extracellular binding domain is capable of binding to the antigen-binding molecule after cleavage of the linker.
[20] The pharmaceutical composition of [18] or [19], wherein the granzyme B variant is the granzyme B variant of [1], [2], or [5].
[21] The pharmaceutical composition of any one of [18] to [20], which comprises the cell expressing the chimeric receptor.
[22] The pharmaceutical composition of [21], wherein the chimeric receptor and the granzyme B variant are expressed in the same T cell.
[23] The pharmaceutical composition of any one of [13] and [15] to [22], wherein the chimeric receptor is a chimeric antigen receptor.
[A1] A granzyme B variant comprising one or more amino acid residue mutations selected from 1) to 20) below relative to human wild-type granzyme B:
1) 43T, 43E, 43N, or 43V; 2) 44L or 44F; 3) 45Q, 45L, or 45A; 4) 46I, 46E, 46F, or 46Q; 5) 47V; 6) 48F or K; 7) 99L; 8) 106A; 9) 149M; 10) 151L; 11) 155P; 12) 172L; 13) 175Q, 175E, or 175I; 14) 183P; 15) 184L; 16) 200R; 17) 217I; 18) 219F; 19) 222G or 222S; and 20) 229V.
[A2] The granzyme B variant of [A1], which comprises one or more amino acid residue mutations selected from 1) to 20) below relative to human wild-type granzyme B:
1) Q43T, Q43E, Q43N, or Q43V; 2) K44L or K44F; 3) S45Q, S45L, or S45A; 4) L46I, L46E, L46F, or L46Q; 5) K47V; 6) R48F; 7) A99L; 8) S106A; 9) Q149M; 10) A151L; 11) K155P; 12) K172L; 13) S175Q, S175E, or S175I; 14) S183P; 15) T184L; 16) K200R; 17) V217I; 18) Y219F; 19) N222G or N222S; and 20) A229V.
[A3] The granzyme B variant of [A1], wherein the amino acid residue mutations are any of 1) to 12) below:
[A4] The granzyme B variant of [A3], wherein the amino acid residue mutations are any of 1) to 12) below:
[A5] The granzyme B variant of any one of [A1] to [A4], which comprises one or more amino acid residue mutations relative to human wild-type granzyme B shown in SEQ ID NO: 1.
[A6] The granzyme B variant of any one of [A1] to [A5], wherein protease activity is enhanced more than that of human wild-type granzyme B.
[A7] The granzyme B variant of any one of [A1] to [A6], which has resistance to an inhibitor to human wild-type granzyme B.
[A8] The granzyme B variant of [A7], wherein the inhibitor is PI-9 or heparin.
[A9] An isolated nucleic acid encoding the granzyme B variant of any one of [A1] to [A8].
[A10] A vector comprising the isolated nucleic acid of [A9].
[A11] A cell transformed or transduced with the isolated nucleic acid of [A9] or the vector of [A10].
[A12] A cell expressing the granzyme B variant of any one of [A1] to [A8].
[A13] A pharmaceutical composition comprising the isolated nucleic acid of [A9], the vector of [A10], or the cell of [A11] or [A12].
[A14] A pharmaceutical composition comprising the granzyme B variant of any one of [A1] to [A8].
[A15] The pharmaceutical composition of any one of [12] to [14], wherein the granzyme B variant is the granzyme B variant of any one of [A1] to [A5].
[A16] The pharmaceutical composition of [A15], which comprises the cell expressing the receptor.
[A17] The pharmaceutical composition of [A16], wherein the receptor and the granzyme B variant are expressed in the same T cell.
[A18] The pharmaceutical composition of [18] or [19], wherein the granzyme B variant is the granzyme B variant of any one of [A1] to [A5].
[A19] The pharmaceutical composition of [A18], which comprises the cell expressing the chimeric receptor.
[A20] The pharmaceutical composition of [A19], wherein the chimeric receptor and the granzyme B variant are expressed in the same T cell.
[A21] The pharmaceutical composition of any one of [A15] to [A20], wherein the receptor is a chimeric antigen receptor.
[B1] The granzyme B variant of [3] or [A6] or the pharmaceutical composition of [12] or [18], wherein in vitro protease activity of the granzyme B variant is 1.5 times or more than that of human wild-type granzyme B.
[B2] The granzyme B variant or pharmaceutical composition of [B1], wherein the in vitro protease activity of the granzyme B variant is twice or more than that of human wild-type granzyme B.
[B3] The granzyme B variant of [4] or [A7] or the pharmaceutical composition of [12] or [18], wherein in vitro protease activity in the presence of the inhibitor is 1.1 times or more, 1.2 times or more, 1.3 times or more, 1.4 times or more, or 1.5 times or more than that of human wild-type granzyme B.
[B4] The granzyme B variant or pharmaceutical composition of [B3], wherein the in vitro protease activity in the presence of the inhibitor is 1.1 times or more, 1.2 times or more, 1.3 times or more, 1.4 times or more, 1.5 times or more, or twice or more than that of human wild-type granzyme B.
[B5] The granzyme B variant or pharmaceutical composition of [B3] or [B4], wherein the inhibitor is PI-9 or heparin.
[B6] An isolated nucleic acid encoding the granzyme B variant of any one of [B1] to [B5].
[B7] A vector comprising the isolated nucleic acid of [B6].
[B8] A cell transformed or transduced with the isolated nucleic acid of [B6] or the vector of [B7].
[B9] A cell expressing the granzyme B variant of any one of any one of [B1] to [B5].
[B10] A pharmaceutical composition comprising the isolated nucleic acid of [B6], the vector of [B7], or the cell of [B8] or [B9].
[B11] A pharmaceutical composition comprising the granzyme B variant of any one of [B1] to [B5].
[B12] The pharmaceutical composition of any one of [B1] to [B5],
wherein the receptor is a chimeric receptor which comprises an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain, and binds to the ligand via the extracellular binding domain.
[B13] The pharmaceutical composition of any one of [B1] to [B5], wherein the receptor is a T-cell receptor whose ligand is a neoantigen.
[B14] The pharmaceutical composition of any one of [B1] to [B5], [B12], and [B13], wherein the granzyme B variant is the granzyme B variant of any one of [1], [2], and [A1] to [A5].
[B15] The pharmaceutical composition of any one of [B1] to [B5] and [B12] to [B14], which comprises the cell expressing the receptor.
[B16] The pharmaceutical composition of [B15], wherein the receptor and the granzyme B variant are expressed in the same T cell.
[B17] The pharmaceutical composition of any one of [B1] to [B5],
wherein the antigen-binding molecule comprises a linker that is cleavable by a protease, and
wherein the extracellular binding domain is capable of binding to the antigen-binding molecule after cleavage of the linker.
[B18] The pharmaceutical composition of any one of [B1] to [B5], and [B17], wherein the granzyme B variant is the granzyme B variant of any one of [1], [2] and [A1] to [A5].
[B19] The pharmaceutical composition of any one of [B1] to [B5], [B17], and [B18], which comprises the cell expressing the chimeric receptor.
[B20] The pharmaceutical composition of [B19], wherein the chimeric receptor and the granzyme B variant are expressed in the same T cell.
[B21] The pharmaceutical composition of any one of [B12] and [B14] to [B20], wherein the chimeric receptor is a chimeric antigen receptor.
[C1] The pharmaceutical composition of any one of [10] to [23], which is for use in the treatment or prevention of cancer.
[C2] The pharmaceutical composition of any one of [10] to [23], which is for use in the treatment or prevention of an inflammatory disease.
[C3] The granzyme B variant of any one of [1] to [5], [A1] to [A8], and [B1] to [B5] or the cell of [8] or [9], which is for use in the treatment or prevention of cancer or an inflammatory disease.
[C4] A method of treating or preventing cancer or an inflammatory disease, wherein the method comprises administering the granzyme B variant of any one of [1] to [5], [A1] to [A8], and [B1] to [B5] or the cell of [8] or [9].
[C5] The method of [C4], further comprising administering a cell expressing a receptor, wherein the receptor activates the cell expressing the receptor by its binding to a ligand.
[C6] The method of [C5], wherein the receptor is a chimeric receptor that comprises an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain, and binds to the ligand via the extracellular binding domain.
[C7] The method of [C6], further comprising administering an antigen-binding molecule, wherein the antigen-binding molecule has an ability to bind to a target antigen, and wherein the chimeric receptor is capable of binding to a cell expressing the target antigen via the binding of the extracellular binding domain to the antigen-binding molecule.
[C8] The method of [C7], wherein the antigen-binding molecule comprises a linker that is cleavable by a protease, and wherein the extracellular binding domain is capable of binding to the antigen-binding molecule after cleavage of the linker.
[C9] The method of [C5], wherein the receptor is a T cell receptor whose ligand is a neoantigen.
[C10] The method of any one of [C5] to [C9], wherein the administration is an administration of a T cell expressing the receptor and the granzyme B variant.
[C11] Use of the granzyme B variant of any one of [1] to [5] or the cell of [8] or [9] in the manufacture of a therapeutic agent or preventive agent for cancer or an inflammatory disease.
[D1] A method of producing an isolated nucleic acid encoding the granzyme B variant of any one of [1] to [5], [A1] to [A8], and [B1] to [B5].
[D2] A method of producing a vector comprising the isolated nucleic acid of [6], [A9], or [B6].
[D3] A method of producing a cell transformed or transduced with the isolated nucleic acid of [6], [A9] or [B6], or the vector of [7], [A10] or [B7].
[D4] A method of producing a cell expressing the granzyme B variant of any one of [1] to [5], [A1] to [A8], and [B1] to [B5].
In one non-limiting embodiment, the granzyme B variants of the present disclosure have higher protease activity and/or resistance to inhibitors compared to wild-type granzyme B. Pharmaceutical compositions comprising a granzyme B variant having such advantageous effects or a cell expressing the variant of the present disclosure are more advantageous than wild-type granzyme B and the prior art granzyme B variants in inducing cell death of target cells. Furthermore, cell death specific to target cells can be induced by using the granzyme B variants of the present disclosure in combination with pharmaceuticals using cells expressing a receptor and/or a therapeutic antibody.
Unless defined otherwise, technical and scientific terms used herein have the same meaning as commonly understood by one skilled in the art to which the present invention belongs. Singleton et al., Dictionary of Microbiology and Molecular Biology 2nd ed., J. Wiley & Sons (New York, N.Y. 1994), and March, Advanced Organic Chemistry Reactions, Mechanisms and Structure 4th ed., John Wiley & Sons (New York, N.Y. 1992), provide one skilled in the art with a general guide to many of the terms used in the present application. All references cited herein, including patent applications and publications, are incorporated herein by reference in their entirety.
For purposes of interpreting the present specification, the following definitions apply and whenever appropriate, terms used in the singular also include the plural and vice versa. It is to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. In the event that any definition set forth below conflicts with any document incorporated herein by reference, the definition set forth below shall control.
The term “granzyme B,” as used herein, refers to any wild-type granzyme B from any vertebrate source, including mammals such as primates (e.g., humans) and rodents (e.g., mice and rats), unless otherwise indicated. The term encompasses “full-length” unprocessed granzyme B as well as any form of granzyme B that results from processing in the cell. The term also encompasses naturally occurring variants of granzyme B, e.g., splice variants or allelic variants. The amino acid sequence of an exemplary human wild-type granzyme B is shown in SEQ ID NO: 1 (NCBI Reference Sequence. NP_004122.2), but is not limited thereto and includes variants of which amino acid sequences are partially different. Such variants include human wild-type granzyme B represented by the amino acid sequence having 90% or more, 95% or more, 97% or more, or 99% or more sequence homology with SEQ ID NO: 1.
As used herein, a “mutation” and an “alteration” are interchangeably used and include an “addition” of an amino acid residue to an amino acid sequence, a “deletion” of an amino acid residue from an amino acid sequence, an “insertion” of an amino acid residue into an amino acid sequence, and/or a “substitution” of an amino acid residue in an amino acid sequence. For obtaining a variant (mutant) with a desired feature (e.g., protease activity or resistance to inhibitors), any combination of an addition, deletion, insertion, and substitution can be introduced. In one embodiment, the granzyme B variants of the present disclosure comprise one or more amino acid residue substitutions.
When the position of each amino acid in granzyme B is indicated herein, the corresponding amino acid number in the amino acid sequence of human wild-type granzyme B exemplified in SEQ ID NO: 1 (in the case of SEQ ID NO: 1, the consecutive number in the amino acid sequence in which the position of the N-terminal amino acid is 1) is designated. For example, when a granzyme B variant of the present disclosure is shown as “comprising the amino acid residue F (Phe) at position 44”, it means that the amino acid residue at position 44 from the N-terminal side which constitutes the granzyme B variant is F (Phe).
Moreover, when an amino acid alteration in granzyme B is indicated herein, the amino acid residues before (i.e., wild-type granzyme B) and after the alteration at the position altered are indicated respectively to the left and right, or the left or right, of the amino acid number of the position (e.g., in single-letter notation). For example, when the amino acid residue at the position corresponding to the amino acid residue K (Lys) at position 44 from the N-terminal side in the amino acid sequence shown in SEQ ID NO: 1 is altered to F (Phe), the amino acid alteration is herein represented as K44F. Furthermore, when simply indicating that the amino acid residue at position 44 from the N-terminal side in granzyme B is altered to F (Phe), it is represented as 44F.
Even if the amino acid sequence of granzyme B to be altered has part different from the sequence shown in SEQ ID NO: 1, those skilled in the art can appropriately determine where the positions of alterations shown herein actually correspond to in granzyme B to be altered (e.g., by performing sequence alignment).
In the present disclosure, the granzyme B variant comprises one or more amino acid residues selected from 1) to 20) below:
1) T, E, N or V at position 43; 2) L or F at position 44; 3) Q, L or A at position 45; 4) I, E, F or Q at position 46; 5) V at position 47; 6) F or K at position 48; 7) L at position 99; 8) A at position 106; 9) M at position 149; 10) L at position 151; 11) P at position 155; 12) L at position 172; 13) Q, E or I at position 175; 14) P at position 183; 15) L at position 184; 16) R at position 200; 17) I at position 217; 18) F at position 219; 19) G or S at position 222; and 20) V at position 229.
In another aspect, the granzyme B variant of the present disclosure comprises any one of the combination of amino acid residues of 1) to 12) below:
1) L at position 44, K at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
2) L at position 44, E at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
3) F at position 44, K at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
4) F at position 44, E at position 48, P at position 155, L at position 172, I at position 175, and R at position 200;
5) L at position 44, I at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
6) L at position 44, E at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
7) L at position 44, F at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
8) L at position 44, Q at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
9) F at position 44, I at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
10) F at position 44, E at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
11) F at position 44, F at position 46, P at position 155, L at position 172, I at position 175, and R at position 200;
12) F at position 44, Q at position 46, P at position 155, L at position 172, I at position 175, and R at position 200.
“Protease activity” herein refers to, especially in the context of granzyme B, the activity of granzyme B to cleave its substrate. Methods of evaluating the protease activity of granzyme B are well known to those skilled in the art, and various activity measurement kits and synthetic substrates are commercially available. As examples of such synthetic substrates, synthetic peptides having a recognition sequence of granzyme B (e.g., Ile-Glu-Pro-Asp (IEPD)) which are labeled with a detectable substance (e.g., p-nitroanilide (pNA)) are known (e.g., Ac-IEPD-pNA). Cleavage of a synthetic substrate by granzyme B releases a free detectable substance, which can be quantitatively determined with a fluorometer or a spectrophotometer. As an example, evaluation of the protease activity of granzyme B variants can be performed by the method described in Example 4 of the present disclosure. For example, evaluation of the protease activity in the presence of inhibitors can be performed using the evaluation system described in Example 4 and under the same concentration conditions of granzyme B and inhibitors as in the Example.
The protease activity of the granzyme B variants of the present disclosure is preferably enhanced compared to that of wild-type granzyme B, and is, for example, preferably 1.1 times or more, 1.2 times or more, 1.3 times or more, 1.4 times or more, or 1.5 times or more higher, more preferably twice or more or 2.5 times or more higher, and particularly preferably 3 times or more higher than the protease activity of wild-type granzyme B.
The protease activity of wild-type granzyme B is known to be inhibited by “inhibitors” such as PI-9 and heparin. The granzyme B variants of the present disclosure preferably have resistance to such inhibitors. Herein, “resistance to an inhibitor” refers to an ability to exert protease activity higher than that of wild-type granzyme B in the presence of such an inhibitor. The protease activity of the granzyme B variants of the present disclosure in the presence of such an inhibitor is preferably 1.1 times or more, 1.2 times or more, 1.3 times or more, 1.4 times or more, or 1.5 times or more higher, more preferably twice or more, 2.5 times or more, 3 times or more, or 3.5 times or more higher, and particularly preferably 4 times or more, 4.5 times or more, 5 times or more, or 5.5 times or more higher than that of wild-type granzyme B.
An “isolated” nucleic acid refers to a nucleic acid molecule that has been separated from a component of its natural environment. An isolated nucleic acid includes a nucleic acid molecule contained in cells that ordinarily contain the nucleic acid molecule, but the nucleic acid molecule is present extrachromosomally or at a chromosomal location that is different from its natural chromosomal location.
The term “vector,” as used herein, refers to a nucleic acid molecule capable of propagating another nucleic acid to which it is linked. The term includes the vector as a self-replicating nucleic acid structure as well as the vector incorporated into the genome of a host cell into which it has been introduced. Certain vectors are capable of directing the expression of nucleic acids to which they are operatively linked. Such vectors are referred to herein as “expression vectors.”
The terms “host cell,” “host cell line,” and “host cell culture” are used interchangeably and refer to cells into which exogenous nucleic acid has been introduced, including the progeny of such cells. Host cells include “transformants” and “transformed cells,” or “transductant” and “transduced cells,” which include the primary transformed cell or transduced cell and progeny derived therefrom without regard to the number of passages. Progeny may not be completely identical in nucleic acid content to a parent cell, but may contain mutations. Mutant progeny that have the same function or biological activity as screened or selected for in the originally transformed cell or transduced cell are included herein.
Herein, unless otherwise indicated, a “cell expressing granzyme B” may be a cell expressing endogenous granzyme B or a cell expressing granzyme B by gene transfer. As cells expressing endogenous granzyme B, for example, cytotoxic lymphocytes—T cells and NK cells—are known. On the other hand, cells that are transfected to express granzyme B are not limited to T cells and NK cells, and recombinant granzyme B can be obtained by expressing recombinant granzyme B in various cells (for example, by purifying granzyme B from their culture supernatant). Furthermore, it is possible to introduce a gene expressing granzyme B into cells (e.g., peripheral blood mononuclear cells (PBMCs)) derived from an individual (e.g., a healthy donor or a patient suffering from a particular disease), and to administer the transgenic cells to the same or different individual. Transgenic cells expressing granzyme B may be treated to differentiate into a particular cell type (e.g., cytotoxic T cells) and then administered to an individual. As a method of introducing a gene encoding granzyme B into cells, various gene transfer techniques well known to those skilled in the art can be used.
Cells expressing granzyme B may be administered in combination with cells expressing a chimeric receptor. Moreover, cells expressing both granzyme B and a chimeric receptor may be used, and such cells can be produced by simultaneous or separate gene transfer of granzyme B and a chimeric receptor.
When a granzyme B variant is expressed in a cell expressing endogenous granzyme B, such as a T cell or NK cell, the endogenous wild-type granzyme B in the cell may or may not be knocked out.
The term “pharmaceutical formulation” or “pharmaceutical composition” refers to a preparation which is in such form as to permit the biological activity of an active ingredient contained therein to be effective, and which contains no additional components which are unacceptably toxic to a subject to which the formulation or composition would be administered. An “active ingredient” can be constituted as an antibody, polypeptide or the like, or as a cell expressing an antibody, polypeptide or the like (e.g., a granzyme B variant of the present disclosure). For example, when a cell transformed or transduced with a nucleic acid encoding a granzyme B variant of the present disclosure or a vector comprising such a nucleic acid is administered to a patient for purposes of treatment or prevention, a preparation comprising such a cell can be referred to as a “pharmaceutical formulation” or “pharmaceutical composition”.
A “pharmaceutically acceptable carrier” refers to an ingredient in a pharmaceutical formulation or pharmaceutical composition, other than an active ingredient, which is nontoxic to a subject. A pharmaceutically acceptable carrier includes, but is not limited to, a buffer, excipient, stabilizer, or preservative.
An “individual” or “subject” is a mammal. Mammals include, but are not limited to, domesticated animals (e.g., cows, sheep, cats, dogs, and horses), primates (e.g., humans and non-human primates such as monkeys), rabbits, and rodents (e.g., mice and rats). In certain embodiments, the individual or subject is a human.
In one aspect, the present disclosure provides granzyme B variants, cells expressing a granzyme B variant, or pharmaceutical compositions comprising them.
In one embodiment, the pharmaceutical compositions of the present disclosure can be used in combination with a cell expressing a receptor. The receptor is one that activates a cell expressing the receptor by its binding to a ligand, and includes, for example, a chimeric receptor that binds to a ligand via the extracellular binding domain and a T-cell receptor whose ligand is a neoantigen, but is not limited thereto. The pharmaceutical compositions of the present disclosure may comprise a cell expressing a receptor and a cell expressing a granzyme B variant, and the receptor and the granzyme B variant may be expressed in the same cell (e.g., a T cell).
Such pharmaceutical compositions of the present disclosure can be used in combination with an antigen-binding molecule that is capable of binding to the extracellular binding domain of a chimeric receptor. The antigen-binding molecule has an ability to bind to a target antigen, and the chimeric receptor can bind to a cell expressing the target antigen via the binding of its extracellular binding domain to the antigen-binding molecule. In a certain embodiment, the antigen-binding molecule comprises a linker that is cleavable by a protease, and the extracellular binding domain can bind to the antigen-binding molecule after cleavage of the linker. The pharmaceutical compositions of the present disclosure may comprise a cell expressing a chimeric receptor and a cell expressing a granzyme B variant, and an antigen-binding molecule capable of binding to the extracellular binding domain of the chimeric receptor. The receptor and the granzyme B variant may be expressed in the same cell (e.g., a T cell).
When one or more of a granzyme B variant, a cell expressing a granzyme B variant, a cell expressing a receptor, a cell expressing a receptor and a granzyme B variant, and an antigen-binding molecule capable of binding to the extracellular binding domain of a chimeric receptor are used in combination, they can be used (e.g., administered to an individual) simultaneously, separately, or sequentially.
In one embodiment, the pharmaceutical compositions of the present disclosure are for use in damaging cells, inducing cell death, suppressing cell proliferation, or treating or preventing cancer or inflammatory diseases.
The term “chimeric receptor” refers to a recombinant polypeptide comprising at least an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain, which polypeptide provides specificity for a target cell, e.g., a cancer cell, and produces intracellular signals when expressed in an immune effector cell. The term “chimeric antigen receptor” or “CAR” means a chimeric receptor whose extracellular binding domain binds to an antigen.
The term “extracellular binding domain” means any proteinaceous molecule or part thereof that can specifically bind to a given molecule such as an antigen, and includes, for example, a single-chain antibody (scFv) in which a light chain (VL) and a heavy chain (VH) of a monoclonal antibody variable region specific to a tumor antigen or the like are connected in tandem. An extracellular binding domain can be rephrased as an extracellular recognition domain.
The term “transmembrane domain” includes a polypeptide that is located between the extracellular binding domain and the intracellular signaling domain and has the function of penetrating the cell membrane.
The term “intracellular signaling domain” means any oligopeptide domain or polypeptide domain that is known to function to transmit a signal that causes activation or inhibition of a biological process within a cell, e.g., activation of an immune cell such as a T cell or NK cell, and the domain comprises at least one stimulatory molecule signaling domain derived from a T-cell stimulatory molecule and at least one costimulatory molecule signaling domain derived from a T-cell costimulatory molecule.
The term “T-cell receptor whose ligand is a neoantigen” herein includes T-cell receptors designed to recognize neoantigens, which are mutant antigens resulting from genetic mutations in cancer cells.
Herein, the term “antigen-binding molecule” refers, in its broadest sense, to a molecule that specifically binds to an antigenic determinant (epitope). In one embodiment, the antigen-binding molecule is an antibody, antibody fragment, or antibody derivative. In one embodiment, the antigen-binding molecule is a non-antibody protein, or a fragment thereof, or a derivative thereof.
Herein, “antigen-binding domain” refers to a region that specifically binds and is complementary to the whole or a portion of an antigen. Herein, an antigen-binding molecule comprises an antigen-binding domain. When the molecular weight of an antigen is large, an antigen-binding domain can only bind to a particular portion of the antigen. The particular portion is called “epitope”. In one embodiment, an antigen-binding domain comprises an antibody fragment which binds to a particular antigen. An antigen-binding domain can be provided from one or more antibody variable domains. In a non-limiting embodiment, the antigen-binding domains comprise both the antibody light chain variable region (VL) and antibody heavy chain variable region (VH). Examples of such antigen-binding domains include “single-chain Fv (scFv)”, “single-chain antibody”, “Fv”, “single-chain Fv2 (scFv2)”, “Fab”, and “Fab′”. In other embodiments, an antigen-binding domain comprises a non-antibody protein which binds to a particular antigen, or a fragment thereof. In a specific embodiment, an antigen-binding domain comprises a hinge region.
Herein, “specifically binds” means binding in a state where one of the molecules involved in specific binding does not show any significant binding to molecules other than a single or a number of binding partner molecules. Furthermore, it is also used when an antigen-binding domain is specific to a particular epitope among multiple epitopes contained in an antigen. When an epitope bound by an antigen-binding domain is contained in multiple different antigens, antigen-binding molecules comprising the antigen-binding domain can bind to various antigens that have the epitope.
The term “antibody” herein is used in the broadest sense and encompasses various antibody structures, including but not limited to monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments so long as they exhibit the desired antigen-binding activity.
“Native antibodies” refer to naturally occurring immunoglobulin molecules with varying structures. For example, native IgG antibodies are heterotetrameric glycoproteins of about 150,000 daltons, composed of two identical light chains and two identical heavy chains that are disulfide-bonded. From N- to C-terminus, each heavy chain has a variable region (VH), also called a variable heavy domain or a heavy chain variable domain, followed by three constant domains (CH1, CH2, and CH3). Similarly, from N- to C-terminus, each light chain has a variable region (VL), also called a variable light domain or a light chain variable domain, followed by a constant light (CL) domain. The light chain of an antibody may be assigned to one of two types, called kappa (κ) and lambda (λ), based on the amino acid sequence of its constant domain.
The term “variable region” or “variable domain” refers to the domain of an antibody heavy or light chain that is involved in binding the antibody to antigen. The variable domains of the heavy chain and light chain (VH and VL, respectively) of a native antibody generally have similar structures, with each domain comprising four conserved framework regions (FRs) and three hypervariable regions (HVRs). (See, e.g., Kindt et al., Kuby Immunology, 6th ed., W.H. Freeman and Co., page 91 (2007).) A single VH or VL domain may be sufficient to confer antigen-binding specificity. Furthermore, antibodies that bind a particular antigen may be isolated using a VH or VL domain from an antibody that binds the antigen to screen a library of complementary VL or VH domains, respectively. See, e.g., Portolano et al., J. Immunol. 150:880-887 (1993); Clarkson et al., Nature 352:624-628 (1991).
In several embodiments, the present disclosure provides methods of damaging cells, inducing cell death, suppressing cell proliferation, treating inflammatory diseases, treating cancer, or preventing cancer, the method comprising administering an effective amount of a granzyme B variant, a cell expressing the granzyme B variant, or a pharmaceutical composition comprising them of the present disclosure (hereinafter may be collectively referred to as “pharmaceutical composition and such of the present disclosure”). In some embodiments, the “effective amount” in the present invention means a dose of the pharmaceutical composition and such of the present disclosure that is effective in damaging cells, inducing cell death, suppressing cell proliferation, treating inflammatory diseases, treating cancer, or preventing cancer in individuals.
In several embodiments, “treatment/treating/therapeutic” according to the present invention means that a pharmaceutical composition and such of the present disclosure decreases the number of cancer cells in individuals, suppresses cancer cell proliferation, decreases tumor size (volume and/or weight), suppresses tumor enlargement, suppresses infiltration of cancer cells into peripheral organs, suppresses cancer cell metastasis, or ameliorates various symptoms caused by cancer. Furthermore, in several embodiments, “prevention/preventing/prophylactic” according to the present invention refers to inhibiting increase in the number of cancer cells due to repopulation of cancer cells that have decreased, inhibiting repopulation of cancer cells whose proliferation have been suppressed, and inhibiting the decreased tumor size (volume and/or weight) to become large again.
The granzyme B variants of the present disclosure can be used in combination with administration of a cell expressing a receptor. An example of the receptor includes a chimeric receptor comprising an extracellular binding domain, a transmembrane domain, and an intracellular signaling domain. Furthermore, another example includes a T-cell receptor designed to recognize a neoantigen that cannot be recognized by normal T cells. As an embodiment of combinations of techniques utilizing these receptors and the granzyme B variants of the present disclosure, there is a means of collecting T cells from a patient, introducing a gene encoding a chimeric receptor (e.g., a chimeric antigen receptor) and a gene encoding a granzyme B variant into the T cells, and transferring them back into the patient. (Without being limited to that, it is also possible to separately introduce the genes and transfer the T cells into the patient.) The chimeric antigen receptor recognizes a surface antigen of a cell such as a cancer cell to activate the T cells, and enhanced cytotoxic activity is exerted by a granzyme B variant of the present disclosure, and thereby a high therapeutic effect is expected.
Similarly, by introducing a gene encoding a T-cell receptor whose ligand is a neoantigen and a gene encoding a granzyme B variant into T cells collected from a patient, and then transferring them back into the patient, a high therapeutic effect from the combination is expected.
Moreover, in combinations of the granzyme B variants of the present disclosure and chimeric receptors, combinations further combined with antigen-binding molecules (such as antibodies) can also be used. In this case, an antigen-binding molecule has an ability to bind to a target antigen, and a chimeric receptor can bind to cells expressing the target antigen via the binding of the extracellular binding domain to the antigen-binding molecule. As an embodiment of the antigen-binding molecule, the antigen-binding molecule is prepared in advance to comprise a linker that is cleavable by a protease, and the chimeric receptor can be designed to be capable of binding to the antigen-binding molecule after cleavage of the linker. As an embodiment of such combinations, there is a means of collecting T cells from a patient, introducing a gene encoding a chimeric receptor and a gene encoding a granzyme B variant into the T cells, transferring them back into the patient, and separately administering a pharmaceutical composition comprising an antigen-binding molecule to the patient.
Herein below, Examples of construction, expression, purification, gene transfer, and use for treating injuries and diseases of variant granzymes are described, but methods of performing this patent are not limited to these Examples.
The sequence of human wild-type granzyme B (NCBI Reference Sequence. NP_004122.2) was genetically synthesized. The nucleotide sequences respectively encoding an artificial secretion signal sequence (MGILPSPGMPALLSLVSLLSVLLMGCVAETG (SEQ ID NO: 3)) and an enterokinase recognition sequence (DDDDK (SEQ ID NO: 4)) were fused to the 5′-end of the nucleotide sequence encoding amino acid numbers 21-247 (SEQ ID NO: 2) of the ORF encoding granzyme B, and the nucleotide sequence encoding a histidine tag was added to the C-terminal side (J Vis Exp. 2015 Jun. 10; (100): e52911). The nucleotide sequence encoding that sequence (SEQ ID NO: 5) was inserted into a mammalian cell expression vector.
Furthermore, when an amino acid alteration position in granzyme B is indicated herein, the corresponding amino acid number in the amino acid sequence of human wild-type granzyme B (NCBI Reference Sequence. NP_004122.2) shown in SEQ ID NO: 1 is designated.
Substitutions of a single amino acid residue with respect to human wild-type granzyme B and substitutions of multiple amino acid residues combining them were performed using PCR reactions by a method known to those skilled in the art.
The positions of amino acids to be altered were selected by identifying amino acid residues close to the substrate-binding site based on the crystal structure of human wild-type granzyme B (the underlined amino acids in
Moreover, by similar methods, nucleotide sequences encoding granzyme B variants with multiple amino acid substitutions were produced.
The nucleotide sequences encoding granzyme B produced in Example 2 were transfected into 1 mL of Expi293 (Invitrogen) culture medium by the method specified by the supplier. After four days, the culture supernatant was collected, and enterokinase was added at a final concentration of 0.3 μg/mL and reacted at 4° C. for 16 hours. One-tenth volume of a binding buffer (250 mM Tris, 3M NaCl, pH 7.5) was added to the reaction solution, and then 50 μL of Ni Sepharose Excel (GE healthcare, 17371201) suspended in an equilibrium buffer (25 mM Tris-HCl, 500 mM NaCl, pH 7.5) was added. After reaction at 4° C. for one hour, the reaction solution was added to a filter plate (Merck, MSGVS2210). The granzyme B-bound Ni Sepharose Excel was washed five times with 200 μL of the equilibrium buffer, and then reacted with an elution buffer (25 mM Tris-HCl, 500 mM NaCl, 500 mM Imidazole, pH 7.5) at 4° C. for 15 minutes to elute granzyme B. The concentration of the purified granzyme B was calculated using the absorbance at 280 nm and the extinction coefficient calculated by the PACE method of the eluted granzyme B solution (Protein Science (1995) 4, 2411-2423).
The expressed and purified granzyme B was suspended in a twice diluted enzyme reaction Buffer (2× Reaction buffer, Promokine, PK-CA577-1068-80) and mixed with a reaction substrate, Ac-IEPD-pNA, at a final concentration of 0.5 mM (Enzo, BML-P133). The absorbance at 405 nm of the reaction solution was measured.
The granzyme B activity shown in
Fold change=(the protease activity of a granzyme B variant)/(the protease activity of wild-type granzyme B)
Furthermore, the protease activity of granzyme B is defined by the following formula.
Protease activity=(the change in absorbance at 405 nm of the reaction solution in unit time)/(unit time)
As a result of measuring 1476 variants in the above-mentioned comprehensive measurement, 33 variants were found to have increased activity relative to wild-type granzyme B, and 1443 variants had lower activity than the wild type. With respect to these 33 alterations that increase the protease activity of granzyme B, multiple variants of granzyme B variants in which multiple mutations had been combined were produced by the methods described in Example 2. Of the variants produced, examples in which the increase in activity was particularly remarkable are shown in Table 1. In Table 1, the positions of amino acid substitutions in the variants refer to the corresponding amino acid numbers in the amino acid sequence of human wild-type granzyme B shown in SEQ ID NO: 1, and the amino acid sequences of the variants indicate the variant amino acid sequences corresponding to amino acid numbers 21-247 of human wild-type granzyme B shown in SEQ ID NO: 1.
When the protease activity was measured in the presence of an inhibitor, wild-type granzyme B or the granzyme B variants were incubated at 37° C. for one hour in the presence of 40 μM heparin (Heparin sodium salt from porcine intestinal mucosa, Sigma-Aldrich, H3393-50KU) or 0.5 μM PI-9 (Recombinant Human Serpin B9/SERPINB9 (C-6His) (Novoprotein, CJ32)) and 0.5 mM DTT, and then mixed with 1 mM Ac-IEPD-pNA solution at a volume ratio of 1:1. The twice diluted enzyme reaction Buffer (2× Reaction buffer, Promokine, PK-CA577-1068-80) was used to prepare all solutions. In measuring the protease activity of the produced variants in the absence of an inhibitor, they were incubated with the enzyme reaction Buffer containing 0.5 mM DTT instead of the inhibitor suspension at 37° C. for one hour, and then mixed with 1 mM Ac-IEPD-pNA solution at a volume ratio of 1:1 and measured. Measurement of the absorbance was performed in the same manner as described in Example 4-1. The results of the measurement are shown in
A secretion signal sequence derived from wild-type granzyme B and a cathepsin C/H recognition sequence are fused to the N-terminal side of the granzyme B variants produced in Example 4 and the amino acid sequence corresponding to amino acid numbers 21-247 of wild-type granzyme B (SEQ ID NO: 1), and a FLAG tag is fused to their C-terminal side. The nucleotide sequences encoding these fusions are transfected into an NK cell line (NKL, ATCC No.) by a mammalian expression vector, pGL4.30 (Promega, E8481). This NK cell line is selected with hygromycin B. The cell lines of granzyme B variants are membrane-permeabilized using eBioscience™ Foxp3/Transcription Factor Staining Buffer Set (Invitrogen, 00-5523-00) by the method specified by one skilled in the art, and are fluorescently stained utilizing an anti-FLAG antibody that recognizes the tag fused to the C-terminus of granzyme B and its isotype control antibody (Biolegend, 637310 and 400508). The cells stained are detected with FACS verse (BD). As a result, a peak associated with granzyme B expression is observed in the cells into which granzyme B is transfected, and it is confirmed that the transfected granzyme B is expressed.
The cell lines expressing granzyme B variants established and a target cell (any one of BxPC-3, HuCCT-1, and MCAS) are added to a 96-well plate, and the anti-EGFR antibody CetuH0-H1076/CetuL4-k0/CetuH0-Kn125/CetuL4-k0, diluted to each concentration, is added. After reaction at 37° C., LDH release associated with cell death is quantitatively determined using Pierce LDH Cytotoxicity Assay Kit (Thermofisher Scientific, 88954) by the method specified by the supplier. As a result, it is shown that the transgenic cells expressing granzyme B variants exhibit stronger cytotoxic activity than the transgenic cell expressing wild-type granzyme B.
Retroviral vectors encoding human wild-type granzyme B and granzyme B variants are prepared utilizing pMCs-IRES-GFP Retroviral Vector (Cell Biolabs, Inc., RTV-040) by the method specified by the supplier.
HLA-A2+ peripheral blood mononuclear cells (PBMCs) derived from healthy donors (Biological Specialty Corp., Colmar, Pa., USA) are isolated by Ficoll-Paque (GE Healthcare, Piscataway, N.J., USA) density gradient centrifugation. The PBMCs are cultured in a 24-well tissue culture plate in AIM V medium (GIBCO brand; Invitrogen) supplemented with 5% human AB serum (Sigma-Aldrich), 1% MEM non-essential amino acids, 1% penicillin-streptomycin, and 100 U/mL recombinant human IL-2 (BioLegend, San Diego, Calif., USA) at 3×106 cells/well, and are activated with 50 ng/mL OKT3 (eBioscience, San Diego, Calif., USA). After two days, the cells are collected for retroviral transduction. For transduction, a 24-well non-tissue culture treated plate (BD Biosciences, Franklin Lakes, N.J., USA) is coated using 10 μg/mL recombinant human fibronectin fragment (RetroNectin; Takara Bio Inc., Otsu, Shiga, Japan) at 0.5 mL/well at 4° C. overnight. After the incubation, the wells are blocked using 1 mL of Hanks' solution (GIBCO brand; Invitrogen) supplemented with 2.5% human AB serum at room temperature for 30 minutes, and washed with Hanks' solution supplemented with 2.5% N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid (HEPES) (GIBCO brand; Invitrogen).
Transduction is performed by a method previously described (Johnson et al., Blood 114, 535-546 (2009)). Briefly, about 2.5 mL of the retroviral supernatant is added to each coated well and then centrifuged at 32° C. for two hours at 2000 g. One point five milliliter of the viral supernatant is removed and 1×106 (0.5 mL) of the activated PBMCs are added to each well in the presence of 100 U/mL IL-2. The plate is centrifuged at 1000 g for 10 minutes and then incubated at 37° C. overnight.
After the transduction, the cells are washed and maintained in the presence of IL-2 (100 U/mL), and used for experiments five days after the transduction. Expression of granzyme B in the transduced human T cells is determined by flow cytometry after staining with an antibody recognizing the FLAG tag labeled at the C-terminus of granzyme B (Biolegend, 637310) or its isotype control antibody (Biolegend, 400508).
The T cells expressing granzymes prepared in Example 8 and a target cell (any one of BxPC-3, HuCCT-1, and MCAS) are added to a 96-well plate, respectively, and the anti-EGFR anti-CD3 bispecific antibody CetuH0-F760nN17/CetuL4-k0/TR01H113-F760nP17/L0011-k0, diluted to each concentration, is added. After reaction at 37° C., LDH release associated with cell death is quantitatively determined using Pierce LDH Cytotoxicity Assay Kit (Thermofisher scientific, 88954) by the method specified by the supplier. As a result, it becomes clear that the transgenic cells expressing granzyme B variants exhibit stronger cytotoxic activity than the transgenic cell expressing wild-type granzyme B.
The cytotoxic activity of the granzyme-transfected T cells produced in Example 8 is also evaluated with BD FACSVerse™ (BD Biosciences). BxPC-3, HuCCT-1, or MCAS, which is a cancer cell, is prepared as a target cell. The target cells are seeded in a 6-well plate at 1×105 cells or 3×105 cells, respectively. The T cells expressing granzyme B variants or wild-type granzyme B are used as effector cells, and are mixed so that the ratio of effector cells to target cells (E:T) is 1:1 or 1:3. Next, the anti-EGFR anti-CD3 bispecific antibody CetuH0-F760nN17/CetuL4-k0/TROIH113-F760nP17/L0011-k0 is added at 10 μg per well. After 48 hours of the addition, the granzyme B-transfected T cells and target cells are collected. Dead cells in the cells collected are stained using Zombie Aqua™ Fixable Viability Kit (BioLegend, 423102), and the granzyme B-expressing T cells are stained using an anti-human CD45 antibody (BioLegend, 304039).
Cytotoxic activity is evaluated by the ratio of residual cancer cells. The ratio of residual cancer cells is calculated as the ratio of CD45-fraction cells in viable cells. These results show enhanced cytotoxic activity of the granzyme-expressing T cells in vitro.
The granzyme B variants of the present disclosure exhibit higher protease activity than wild-type granzyme B, and thus are more useful than wild-type granzyme B in treatments that induce cell death of target cells (e.g., cancer cells). Furthermore, the granzyme B variants of the present disclosure exhibit high protease activity even in the presence of inhibitors to wild-type granzyme B, and are therefore more useful than wild-type granzyme B in treatments that induce cell death in tumors that highly express such inhibitors.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-093777 | May 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/020334 | 5/28/2021 | WO |
