Anti-TNFR2 humanized antibodies and uses thereof

Abstract

The present invention discloses a humanized antibody or an antigen-binding fragment thereof capable of specifically binding to TNFR2, which can regulate the function of immune cells and can be used as a drug for treating diseases associated with immune abnormalities such as tumors.

Description

[Technical field]

[0001] The present invention relates to the fields of biopharmaceuticals and bioengineering, in particular to an anti-TNFR2 humanized antibody or an antigen-binding fragment thereof, and a pharmaceutical composition of said anti-TNFR2 humanized antibody or an antigen-binding fragment thereof and uses thereof. [Background technology]

[0002] Immunity is the body's defense response and is influenced by many genes, proteins, and cells. Immune abnormalities can cause many diseases, including tumors, immunodeficiencies (such as AIDS), allergies, rheumatoid arthritis, and other diseases. In recent years, tumor immunotherapy has emerged as a new treatment and has become a major hot topic in the field of tumor treatment research. Antagonist antibodies, such as anti-PD-1 and anti-CTLA-4 monoclonal antibodies, that target immune checkpoint proteins have been used to treat multiple types of cancer and have brought revolutionary results in significantly extending the survival time of patients with malignant tumors. Summary of the Invention [Problem to be solved by the invention]

[0003] However, there are still many cancer patients who are unresponsive to the antagonist antibody treatment against immune checkpoint proteins or develop resistance or tolerance after temporary treatment. Therefore, it is necessary to develop new drugs for cancer treatment that can be used alone or in combination with other tumor treatments, including the antagonist antibody against immune checkpoint proteins, to further improve efficacy and safety. [Means for solving the problem]

[0004] The inventors have found that human TNFR2 is overexpressed on the surface of human Treg and several types of human tumor cells, suggesting that human TNFR2 may promote tumor development in patients and mediate immune suppression and immune escape in the tumor microenvironment. Regulating the function of Treg cells through TNFR2 to suppress tumor development is believed to be a very potential anti-tumor strategy. The inventors have prepared an antagonist antibody against TNFR2 that 1) specifically binds to TNFR2 and blocks the binding of TNFR2 to its ligand TNFα, thereby inhibiting the proliferation of Treg cells and their mediated inhibitory function, and promoting the expansion of effector T cells and the anti-tumor function mediated by effector T cells and other immune cells; 2) because TNFR2 is highly expressed in human tumor cell lines, this antibody can also directly mediate the killing effect on tumor cells with high expression of TNFR2; and 3) when combined with existing anti-PD-1 / L1, it has a better anti-tumor effect and can form a sustained immune memory. For a description of the antagonistic antibodies against TNFR2, see PCT / CN2020 / 106057, which is incorporated herein by reference in its entirety.

[0005] The present invention provides an anti-TNFR2 humanized antibody or an antigen-binding fragment thereof, as well as a pharmaceutical composition of the anti-TNFR2 humanized antibody or an antigen-binding fragment thereof and uses thereof. [Brief description of the drawings]

[0006] [Figure 1] The binding ability of the test antibodies to human TNFR2 recombinant protein is shown. A, B, and C show the binding ability of the humanized molecules of the test antibodies #001, #219, and #224 to human TNFR2 recombinant protein, respectively, of which WT is the human-mouse chimeric wild-type molecule, and anti-hen egg white lysozyme (anti-Hel-WT) isotype control antibody is the negative control for this experiment. [Diagram 2]The binding ability of the test antibodies to recombinant cynomolgus monkey TNFR2 protein is shown. A, B, and C show the binding ability of the humanized molecules of the test antibodies #001, #219, and #224 to recombinant cynomolgus monkey TNFR2 protein, respectively, in which WT is the human-mouse chimeric wild-type molecule, and anti-hen egg white lysozyme (anti-Hel-WT) isotype control antibody is the negative control for this experiment. [Diagram 3] The figure shows the binding ability of the test antibodies to CHO-TNFR2 cells that highly express human TNFR2. A, B, and C show the binding ability of the humanized molecules of the test antibodies #001, #219, and #224 to CHO-TNFR2 cells, respectively, of which anti-Hel-WT is a negative isotype control antibody. [Figure 4] The binding ability of the test antibodies to Treg cells is shown. A and B are overlay graphs showing the binding of humanized molecules of test antibodies #001 and #219 to Treg, respectively. The hollow peaks are binding diagrams of anti-Hel-WT isotype control antibody, and the solid peaks are binding diagrams of each antibody to Treg cells. Anti-human-IgG1-Fc-PE only and Unstained (blank cell control with no antibody added) are both negative controls, and the antibody concentration is 200 ng / mL. [Diagram 5] Binding of test antibodies to CD8+ T cells in activated cynomolgus monkey PBMCs is shown. A is an overlay graph of test antibodies binding to cynomolgus monkey CD8+ T cells at concentrations of 2 μg / mL and 0.2 μg / mL, respectively. B is the fold mean fluorescence intensity (ratio of mean fluorescence intensity of binding of test sample to mean fluorescence intensity with secondary antibody added) of test antibodies binding to cynomolgus monkey CD8+ T cells at concentrations of 2 μg / mL and 0.2 μg / mL, respectively. Among them, anti-hen egg white lysozyme (anti-Hel) isotype control antibody is the negative control for this experiment. [Figure 6]The test antibody inhibits the interaction between human TNFα and human TNFR2 recombinant protein. A, B and C are the inhibition of TNFα-TNFR2 by the humanized molecules of the test antibody #001, #219 and #224, respectively, among which the anti-hen egg white lysozyme (anti-Hel) isotype control antibody is the negative control of this experiment. [Figure 7] The test antibodies inhibit the interaction between human TNFα and human TNFR2 expressed by CHO-TNFR2 cells. A, B and C indicate that the humanized molecules of test antibodies #001, #219 and #224 inhibit the interaction between TNFα and CHO-TNFR2, respectively, of which anti-Hel is a negative isotype control antibody. [Figure 8] Figure 1 shows the inhibitory effect of the test antibodies on TNFα-induced IκBα degradation. A is the gating strategy of this experiment. B shows the inhibitory effect of the test antibodies on TNFα-induced IκBα degradation, the left graph is a bar graph of the percentage of IκBαlow at various concentrations of antibodies, and the right graph is the antibody concentration gradient vs. the change in percentage of IκBαlow fold over the negative control antibody anti-Hel. The test concentrations of the antibodies are 0.25, 2.5, and 25 μg / mL, respectively, in which cell control refers to untreated Treg cells, TNF refers to Treg cells treated with 10 ng / mL TNFα, and Rat IgG2b-PE is the negative isotype control (anti-Hel) of Anti-IκBα-PE antibody. Each concentration of the test antibodies has a statistical difference compared to the negative isotype control anti-Hel (**p<0.01, ***p<0.001, Two-Way ANOVA Analysis). [Figure 9]Figure 1 shows the inhibition of the test antibodies against TNFα-induced Treg cell proliferation. Figure 2 shows the overlay graph of the effect of different test antibodies and the negative isotype control anti-Hel on Treg proliferation, where the dashed line is anti-Hel and the solid line is the test antibody. Figure 3 shows the inhibitory effect of different antibodies against TNFα-induced Treg proliferation, where the vertical axis is the percentage of Treg proliferation and the horizontal axis is the test antibody. No treatment (i.e., no drug treatment) and anti-Hel are the negative controls of this experimental system. The experimental concentration of each antibody is 12.5μg / mL. Each test antibody has a statistical difference compared to the negative isotype control anti-Hel (**p<0.01, ***p<0.001, One-Way ANOVA Analysis). [Figure 10] Figure 1 shows the inhibitory effect of the test antibodies on the inhibitory activity of Treg on Tcon cell proliferation. Figure 2 shows the overlay graph of the effect of different test antibodies and the negative isotype control anti-Hel on the inhibition of Treg on Tcon cell proliferation, where the dashed line is anti-Hel and the solid line is the test antibody. Figure 3 shows the inhibitory effect of different antibodies on Treg inhibiting Tcon cell proliferation, where the vertical axis is the percentage of Tcon cell proliferation and the horizontal axis is the test antibody. Wherein, No treat (i.e., no drug treatment) and Anti-Hel are the negative controls of this experimental system, and Tcon+beads is Tcon proliferation in the absence of Treg cells, which is the positive control of the experimental system. The experimental concentration of each antibody is 12.5μg / mL. Each test antibody has a statistical difference compared to the negative isotype control anti-Hel (*p<0.05, **p<0.01, One-Way ANOVA Analysis). [Figure 11] The ADCC killing effect of the test antibody is shown. A shows the ADCC killing effect of the test antibody on Treg. B shows the ADCC killing effect of the test antibody on CHO-TNFR2 cells that highly express human TNFR2. Among them, anti-Hel is a negative control antibody. [Figure 12A]Figure 12 shows the expression identification of hTNFR2 and mTNFR2 in blood immune cells of hTNFR2 transgenic mice (TNFR2 HuGEMM). Figure 12A shows the FACS gating strategy of immune cells in blood of TNFR2 HuGEMM (also called hTNFR2-GEMM) mice, and the expression levels of mTNFR2 and hTNFR2 in gated CD4+ T cells, CD8+ T cells, and Treg cells, as well as the FMO control (Fluorescence Minus One control) for gating. [Figure 12B] Figure 12B shows the expression identification of hTNFR2 and mTNFR2 in blood immune cells of hTNFR2 transgenic mice (TNFR2 HuGEMM). Figure 12B shows histograms showing the expression levels of mTNFR2 and hTNFR2 in CD4+ T cells, CD8+ T cells, and Treg cells in the blood of TNFR2 HuGEMM and Balb / c wild-type mice, where dotted line is isotype, dashed line is BALB / c mouse, and solid line is TNFR2 HuGEMM. [Figure 12C] FIG. 12C shows the expression identification of hTNFR2 and mTNFR2 in blood immune cells of hTNFR2 transgenic mice (TNFR2 HuGEMM). FIG. 12C is a statistical graph of the mean fluorescence intensity of mTNFR2 and hTNFR2 in CD4+ T cells, CD8+ T cells, and Treg cells in the blood of TNFR2 HuGEMM and Balb / c wild-type mice. [Figure 13A] TNFR2 antibodies inhibit mTNFα-induced Treg cell proliferation in TNFR2 HuGEMM (abbreviated as GEMM in the figure) mice. 13A shows the levels of Treg cells expressing human TNFR2 and mouse TNFR2 in the spleens of GEMM mice and wild-type WT Balb / c mice. [Figure 13B]13B and 13C show that TNFR2 antibodies inhibit mTNFα-induced Treg cell proliferation in TNFR2 HuGEMM (abbreviated as GEMM in the figure) mice. 13B and 13C show the inhibitory effect of the test TNFR2 antibodies on mTNFα-induced Treg cell proliferation in GEMM mice or WT Balb / c mice in the absence of activator (B) or in the presence of activator (C) Dynabeads mouse T-activator CD3 / CD28. The experimental concentration of each antibody is 10 μg / mL. Each test antibody has a statistical difference compared to the negative isotype control (***p<0.001, ****p<0.0001, One-Way ANOVA Analysis). [Figure 13C] 13B and 13C show that TNFR2 antibodies inhibit mTNFα-induced Treg cell proliferation in TNFR2 HuGEMM (abbreviated as GEMM in the figure) mice. 13B and 13C show the inhibitory effect of the test TNFR2 antibodies on mTNFα-induced Treg cell proliferation in GEMM mice or WT Balb / c mice in the absence of activator (B) or in the presence of activator (C) Dynabeads mouse T-activator CD3 / CD28. The experimental concentration of each antibody is 10 μg / mL. Each test antibody has a statistical difference compared to the negative isotype control (***p<0.001, ****p<0.0001, One-Way ANOVA Analysis). [Figure 14] Figure 2 shows that anti-TNFR2 antibodies dose-dependently inhibit tumor growth in TNFR2 HuGEMM mice. Figures 2A and 2B show that 219-Hu1-mIgG2a and 001-Hu3-mIgG2a administered at doses of 30 mg / kg, 10 mg / kg, and 3 mg / kg, respectively, can dose-dependently inhibit CT26-hTNFR2 KI tumor growth compared to the vehicle control group. [Figure 15]Figure 2 shows that anti-TNFR2 antibodies inhibit tumor growth in TNFR2 HuGEMM mice while not causing weight loss in the mice. Figures A-B show the absolute body weight change in mice after administration of different doses of 219-Hu1-mIgG2a or 001-Hu3-mIgG2a. Figures C-D show the percentage change in body weight in mice after administration of different doses of 219-Hu1-mIgG2a or 001-Hu3-mIgG2a. [Figure 16] Figure 1 shows that anti-TNFR2 antibodies can significantly inhibit tumor growth in two different PBMC donors in a human PBMC immune reconstituted humanized mouse colon cancer tumor model. Figure A shows that anti-TNFR2 antibody 219-Hu1 has significant efficacy in donor #193. Figure B shows that tumor growth in 001-Hu3, 219-Hu1, and Keytruda groups was all significantly inhibited compared to the control antibody group on day 29 after tumor inoculation in donor #272, with statistical difference (****: p<0.0001, vs. isotype, Two Way ANOVA). Figures C-D show that mice in the control and treatment groups all lost weight in donor #193 and donor #272. [Figure 17]This shows that anti-TNFR2 antibody can significantly increase the ratio of CD8+T / Treg cells in tumor-infiltrating immune cells (TILs). A shows the gating strategy of CD4+T, CD8+T, and Treg cells in tumor-infiltrating TILs. B shows the ratio of CD4+T, CD8+T, and Treg cells to CD45+ cells in tumor-infiltrating leukocytes (TILs) after treatment with isotype antibody, 001-Hu3 antibody, and 219-Hu1 antibody in donor #193. C shows the absolute number of CD4+T, CD8+T, and Treg per mg of tumor tissue in TILs after treatment with isotype antibody, 001-Hu3 antibody, and 219-Hu1 antibody in donor #193. D shows the ratio of CD8+T / Treg in TILs after treatment with isotype antibody, 001-Hu3 antibody, and 219-Hu1 antibody in donor #193. E shows the ratio of CD4+T, CD8+T, and Treg to CD45+ cells in TILs after treatment with isotype, 001-Hu3, and 219-Hu1 antibodies in donor #272. F shows the absolute numbers of CD4+T, CD8+T, and Treg per gram of tumor tissue in TILs after treatment with isotype, 001-Hu3, and 219-Hu1 antibodies in donor #272. G shows the ratio of CD8+T / Treg in tumor-infiltrating TILs after treatment with isotype, 001-Hu3, and 219-Hu1 antibodies in donor #272 (*: p<0.05, **: p<0.01, ***: p<0.001, unpaired T test). [Figure 18] 1 shows the tumor volume change curves for each treatment group in the hTNFR2 KI-CT26.1C03 colon cancer model. [Figure 19] Figure 2 shows the body weight change curves of animals in each treatment group in the hTNFR2 KI-CT26.1C03 colon cancer model. This figure shows the absolute body weight change of mice after administration of different doses of 219-Hu1-hIgG1 antibody or the combined anti-mPD-L1 antibody. [Figure 20]Figure 2 shows the weight change curves of animals in each treatment group in the hTNFR2 KI-CT26.1C03 colon cancer model. This figure shows the weight change curves of mice after administration of different doses of 219-Hu1-hIgG1 antibody or combined anti-mPD-L1 antibody. [Figure 21] Changes in tumor weight at the end of the experiment in each treatment group in the hTNFR2 KI-CT26.1C03 colon cancer model. This figure shows the changes in tumor weight measured by isolating the tumors at the end of the experiment after administering different doses of 219-Hu1-hIgG1 antibody or the combined anti-mPD-L1 antibody. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0007] In a first aspect, the invention comprises a humanized antibody or antigen-binding fragment that specifically binds to TNFR2, the antibody or antigen-binding fragment comprising a heavy chain variable region and a light chain variable region, (1) the heavy chain variable region a. A VH sequence shown in any one of SEQ ID NOs: 19 to 27; b. A VH sequence having at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity to any of the sequences selected from SEQ ID NOs: 19 to 27; or c. A VH sequence having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more amino acid insertions, deletions and / or substitutions compared to any of the sequences selected from SEQ ID NOs: 19 to 27; Including, (2) the light chain variable region a. A VL sequence shown in any one of SEQ ID NOs: 28 to 37; b. A VL sequence having at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity to any of the sequences selected from SEQ ID NOs: 28 to 37; or c. A VL sequence having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more amino acid insertions, deletions and / or substitutions compared to any of the sequences selected from SEQ ID NOs: 28 to 37; Including, Optionally, the amino acid insertions, deletions and / or substitutions occur in the FR regions of the heavy chain variable region or / and the light chain variable region, Optionally, the substitutions are conservative amino acid substitutions.

[0008] In some embodiments, in the antibody or antigen-binding fragment described in the present invention, the heavy chain variable region comprises a VH sequence in which the CDRs are completely identical to those of any of SEQ ID NOs: 19 to 27 and the FRs have at least 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity, and the light chain variable region comprises a VL sequence in which the CDRs are completely identical to those of any of SEQ ID NOs: 28 to 37 and the FRs have at least 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity. In some embodiments, the heavy and light chain variable regions comprised in the antibody or antigen-binding fragment of the invention are (1) a combination having a VH represented by SEQ ID NO: 19 and a VL represented by SEQ ID NO: 28; (2) a combination having a VH represented by SEQ ID NO: 20 and a VL represented by SEQ ID NO: 29; (3) A combination having a VH represented by SEQ ID NO: 19 and a VL represented by SEQ ID NO: 30; (4) A combination having a VH represented by SEQ ID NO: 20 and a VL represented by SEQ ID NO: 31; (5) A combination having a VH represented by SEQ ID NO: 19 and a VL represented by SEQ ID NO: 31; (6) A combination having a VH represented by SEQ ID NO: 21 and a VL represented by SEQ ID NO: 32; (7) A combination having a VH represented by SEQ ID NO: 22 and a VL represented by SEQ ID NO: 32; (8) A combination having a VH represented by SEQ ID NO: 23 and a VL represented by SEQ ID NO: 32; (9) A combination having a VH represented by SEQ ID NO: 24 and a VL represented by SEQ ID NO: 32; (10) A combination having a VH represented by SEQ ID NO: 25 and a VL represented by SEQ ID NO: 32; (11) A combination having VH shown in SEQ ID NO: 26 and VL shown in SEQ ID NO: 33; (12) A combination having VH shown in SEQ ID NO: 27 and VL shown in SEQ ID NO: 34; (13) A combination having VH shown in SEQ ID NO: 27 and VL shown in SEQ ID NO: 35; (14) A combination having VH represented by SEQ ID NO: 27 and VL represented by SEQ ID NO: 33; (15) A combination having VH shown in SEQ ID NO: 27 and VL shown in SEQ ID NO: 36; (16) A combination having VH shown in SEQ ID NO: 26 and VL shown in SEQ ID NO: 34; (17) A combination having VH shown in SEQ ID NO: 27 and VL shown in SEQ ID NO: 37; (18) A combination of VH and VL having at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity compared to any of the combinations of sequences (1) to (17). (19) A combination of VH and VL having 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more amino acid insertions, deletions and / or substitutions compared to any of the combinations of sequences (1) to (17) above; or (20) A combination of VH and VL in which the CDRs are completely identical and the FRs have at least 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity compared to any of the combinations of sequences (1) to (17). Selected from Optionally, the amino acid insertions, deletions and / or substitutions occur in the FR regions of the heavy chain variable region or / and the light chain variable region, Optionally, the substitutions are conservative amino acid substitutions.

[0009] In some embodiments, the antibody or antigen-binding fragment described in the present invention comprises a CDR1-VH selected from SEQ ID NO: 1, 7 or 13, a CDR2-VH selected from SEQ ID NO: 2, 8 or 14, a CDR3-VH selected from SEQ ID NO: 3, 9 or 15, a CDR1-VL selected from SEQ ID NO: 4, 10 or 16, a CDR2-VL selected from SEQ ID NO: 5, 11 or 17, and a CDR3-VL selected from SEQ ID NO: 6, 12 or 18.

[0010] In some embodiments, the antibodies or antigen-binding fragments described in the invention have a dissociation constant (KD) of 7 nM or less for binding to human TNFR2 and a dissociation constant (KD) of 5 nM or less for binding to cynomolgus monkey TNFR2.

[0011] In some embodiments, the antibody or antigen-binding fragment according to the invention may or may not comprise a heavy chain constant region and / or a light chain constant region, preferably said heavy chain constant region comprises a full-length heavy chain constant region or a fragment thereof, said fragment may be selected from a CH1 domain, an Fc domain or a CH3 domain, preferably said heavy chain constant region and / or light chain constant region is a human heavy chain constant region and / or a human light chain constant region, preferably said heavy chain constant region may be selected from an IgG heavy chain constant region such as an IgG1 heavy chain constant region, an IgG2 heavy chain constant region, an IgG3 heavy chain constant region or an IgG4 heavy chain constant region, preferably said heavy chain constant region is a human IgG1 heavy chain constant region, a human IgG2 heavy chain constant region, a human IgG3 heavy chain constant region or a human IgG4 heavy chain constant region.

[0012] In some embodiments, the antibody or antigen-binding fragment according to the invention is selected from a monoclonal antibody, a polyclonal antibody, a natural antibody, an engineered antibody, a monospecific antibody, a multispecific antibody (e.g., a bispecific antibody), a monovalent antibody, a multivalent antibody, a full-length antibody, an antibody fragment, Fab, Fab', F(ab')2, Fd, Fv, scFv, or a diabody.

[0013] In some embodiments, the antibody or antigen-binding fragment according to the invention is linked with or without a linker to another molecule, which may be selected from a therapeutic agent or a tracer, preferably, the therapeutic agent is selected from a radioisotope, a chemotherapeutic agent or an immunomodulatory agent, and the tracer is selected from a radiological contrast agent, a paramagnetic ion, a metal, a fluorescent label, a chemiluminescent label, an ultrasound contrast agent or a photosensitizer.

[0014] In some embodiments, the antibody or antigen-binding fragment according to the invention has the following properties: (1) specifically binds to cells expressing TNFR2 on the cell surface; (2) specifically binds to Treg cells; (3) inhibits the binding of TNFα to TNFR2 protein; (4) inhibits the binding of TNFα to TNFR2 expressed on the cell surface; (5) inhibits TNFα-mediated Treg proliferation and / or Treg function; (6) inhibits TNFα-mediated degradation of IκBα; (7) inhibits the inhibition of Tcon cell proliferation by Treg; (8) mediates ADCC function against TNFR2-expressing cells; (9) increases the ratio of CD8+T / Treg cells in tumor-infiltrating immune cells (TIL); and / or (10) inhibits tumor growth.

[0015] In a second aspect, the present invention provides a multispecific antigen-binding molecule comprising at least a first antigen-binding module and a second antigen-binding module, wherein the first antigen-binding module comprises an antibody or antigen-binding fragment according to the present invention, and the second antigen-binding module specifically binds to an antigen other than TNFR2 or binds to a different TNFR2 epitope than the first antigen-binding module, preferably the other antigen is selected from the group consisting of CD3, CD4, CD5, CD8, CD14, CD15, CD16, CD16A, CD19, CD20, CD21, CD22, CD23, CD25, CD33, CD37, The multispecific antibodies are selected from CD38, CD40, CD40L, CD46, CD52, CD54, CD70, CD74, CD80, CD86, CD126, CD138, B7, PD-1, PD-L1, PD-2, CTLA4, PRVIG, TIGHT, HAS, CLDN18.2, MSLN, MUC, Ia, HLA-DR, tenascin, EGFR, VEGF, P1GF, ED-B fibronectin, oncogene product, IL-2, IL-6, IL-15, IL-21, TRAIL-R1 or TRAIL-R2, preferably said multispecific antibodies are "bispecific", "trispecific" or "tetraspecific". In a third aspect, the present invention comprises a chimeric antigen receptor (CAR) comprising an extracellular antigen-binding domain, a transmembrane domain, and an intracellular signalling domain, wherein said extracellular antigen-binding domain comprises a TNFR2 humanised antibody or antigen-binding fragment according to the first aspect of the invention, or comprises a multispecific antigen-binding molecule according to the second aspect of the invention. In a fourth aspect, the present invention comprises an immune effector cell comprising a chimeric antigen receptor according to the third aspect of the invention or comprising a nucleic acid fragment encoding a chimeric antigen receptor according to the third aspect of the invention, preferably said immune effector cell is selected from a T cell, a natural killer cell (NK cell), a natural killer cell (NKT cell), a monocyte, a macrophage, a dendritic cell or a mast cell, said T cell may be selected from an inflammatory T cell, a cytotoxic T cell, a regulatory T cell (Treg) or a helper T cell, preferably said immune effector cell is an allogeneic immune effector cell or an autoimmune cell. In a fifth aspect, the present invention comprises an isolated nucleic acid fragment encoding a TNFR2 humanized antibody or antigen-binding fragment according to the first aspect of the invention, a multispecific antigen-binding molecule according to the second aspect, or a chimeric antigen receptor according to the third aspect. In a sixth aspect, the present invention comprises a vector comprising the nucleic acid fragment according to the fifth aspect. In a seventh aspect, the present invention comprises a host cell comprising a vector according to the sixth aspect, preferably said cell is a prokaryotic or eukaryotic cell, such as a bacterial (E. coli), a fungal (yeast), an insect cell or a mammalian cell (CHO cell line or 293T cell line), preferably said cell lacks a fucosyltransferase, more preferably said fucosyltransferase is FUT8.

[0016] In an eighth aspect, the present invention comprises a method for preparing an antibody or antigen-binding fragment according to any one of the invention or a multispecific antigen-binding molecule according to the invention, said method comprising culturing a cell according to the seventh aspect and isolating the antibody or antigen-binding fragment or multispecific antigen-binding molecule expressed by the cell. In a ninth aspect, the invention comprises a method for preparing an immune effector cell, said method comprising introducing a nucleic acid fragment encoding said CAR into said immune effector cell, and optionally, said method further comprises initiating expression of said CAR by said immune effector cell.

[0017] In a tenth aspect, the present invention comprises a pharmaceutical composition comprising an antibody or antigen-binding fragment according to the invention, a multispecific antigen-binding molecule according to the invention, a chimeric antigen receptor according to the invention, an immune effector cell according to the invention, a nucleic acid fragment according to the invention, a vector according to the invention, a cell according to the invention, and a product prepared by a method according to the invention, preferably said composition further comprises a pharma- ceutically acceptable carrier, diluent or adjuvant, preferably said composition further comprises an additional anti-tumor agent, immunotherapeutic agent or immunosuppressant agent, preferably said additional anti-tumor agent is selected from a PD-1 antibody, a PD-L1 antibody or a CTLA-4 antibody. In an eleventh aspect, the present invention comprises the use of said antibody or antigen-binding fragment, said multispecific antigen-binding molecule, said chimeric antigen receptor, said immune effector cell, said nucleic acid fragment, said vector, said cell, product prepared by said method, and said pharmaceutical composition in the preparation of a medicament for treating and / or preventing a disease associated with an immune dysregulation, preferably said disease associated with an immune dysregulation is a disease associated with Treg cell and / or MDSC function, preferably said disease is a cancer or an autoimmune disease, preferably said cancer is selected from advanced solid tumors resistant to CTLA-4 and PD-1 therapy such as ovarian cancer, advanced epidermal T-cell lymphoma, stage III / IV metastatic colorectal cancer, triple negative breast cancer, pancreatic cancer, non-small cell lung cancer, and / or metastatic melanoma, preferably said autoimmune disease may be selected from rheumatoid arthritis, multiple sclerosis, systemic sclerosis, neuromyelitis optica spectrum disorder, systemic lupus erythematosus, myasthenia gravis, IgG4-related disease. In a twelfth aspect, the present invention comprises a method for treating and / or preventing a disease associated with an immune disorder, said method comprising administering to a subject an effective amount of an antibody or antigen-binding fragment, said multispecific antigen-binding molecule, said chimeric antigen receptor, said immune effector cell, said nucleic acid fragment, said vector, said cell, a product prepared by said method, and said pharmaceutical composition according to the present invention, preferably, said disease associated with an immune disorder is a disease associated with Treg cell and / or MDSC function, preferably , wherein the disease is cancer or an autoimmune disease, preferably, the cancer is selected from advanced solid tumors resistant to CTLA-4 and PD-1 therapy such as ovarian cancer, advanced epidermal T-cell lymphoma, stage III / IV metastatic colorectal cancer, triple negative breast cancer, pancreatic cancer, non-small cell lung cancer, and / or metastatic melanoma, and preferably, the autoimmune disease may be selected from rheumatoid arthritis, multiple sclerosis, systemic sclerosis, neuromyelitis optica spectrum disorder, systemic lupus erythematosus, myasthenia gravis, IgG4-related disease. In a thirteenth aspect, the invention also comprises administering to the subject an additional anti-tumor therapy, e.g. chemotherapeutic agents, targeted therapeutic agents and immunotherapeutic agents, including PD-1 / PD-L1 therapies, such as anti-PD-1 / PD-L1 antibodies, anti-CTLA-4 therapeutic agents, such as anti-CTLA-4 antibodies, preferably said additional anti-tumor therapy is selected from PD-1 / PD-L1 therapies, preferably said PD-1 / PD-L1 therapy is selected from PD-L1 antibodies. In a fourteenth aspect, the present invention comprises a method for detecting TNFR2 in vitro comprising contacting a sample suspected of containing TNFR2 with an antibody or antigen-binding fragment thereof according to the present invention.

[0018] (Definition and explanation of terms) Unless otherwise specified, terms used herein have the meanings commonly understood by those of ordinary skill in the art. For any term expressly defined herein, the meaning of that term shall prevail. As used herein, the term "TNFR2" refers to tumor necrosis factor receptor 2, also known as tumor necrosis factor receptor superfamily member 1B (TNFRSF1B) or CD120b, which is a membrane receptor that binds tumor necrosis factor-α (TNFα). The TNFR2 is preferably human TNFR2.

[0019] As used herein, the terms "anti-tumor necrosis factor receptor 2 antibody," "tumor necrosis factor receptor 2 antibody," "anti-TNFR2 antibody," "TNFR2 antibody," "anti-TNFR2 antibody portion," and / or "anti-TNFR2 antibody fragment" refer to a protein or peptide-containing molecule that comprises at least a portion of an immunoglobulin molecule that can specifically bind to TNFR2, such as, but not limited to, at least one complementarity determining region (CDR) of a heavy or light chain or a ligand binding portion thereof, a heavy or light chain variable region, a heavy or light chain constant region, a framework region, or any portion thereof. TNFR2 antibodies also include antibody-like protein scaffolds that contain BC, DE, and FG structural loops that are structurally and solvent accessible similar to antibody CDRs, such as the tenth fibronectin type III domain (10Fn3). The tertiary structure of the Fn3 domain resembles that of an IgG heavy chain variable region, and by replacing residues of the BC, DE, and FG loops of Fn3 with residues of the CDR-H1, CDR-H2, or CDR-H3 regions from a TNFR2 monoclonal antibody, one skilled in the art can, for example, graft the CDRs of a TNFR2 monoclonal antibody onto a fibronectin scaffold. As used herein, the term "antibody" (Ab) refers to immunoglobulin molecules that specifically bind to or are immunoreactive with a target antigen, including polyclonal, monoclonal, genetically engineered, and other modified forms of antibodies (including, but not limited to, chimeric antibodies, humanized antibodies, fully human antibodies, heteroconjugate antibodies (e.g., bispecific, trispecific, and tetraspecific antibodies, diabodies, triabodies, and tetrabodies), antibody conjugates), and antigen-binding fragments of antibodies (including, for example, Fab', F(ab')2, Fab, Fv, rIgG, and scFv fragments). Also, unless otherwise specified, the term "monoclonal antibody" (mAb) is meant to include intact antibody molecules that are capable of specifically binding to a target protein, as well as incomplete antibody fragments, such as Fab and F(ab')2 fragments, which lack the Fc fragment of intact antibodies (and are cleared more rapidly from the animal cycle) and therefore lack Fc-mediated effector functions (see Wahl et al., J. Nucl. Med. 24:316, 1983, the contents of which are incorporated herein by reference). As used herein, the term "monoclonal antibody" refers to an antibody that is derived from a single clone (including any eukaryotic, prokaryotic, or phage clone) without limitation by the method of production of the antibody. As used herein, the terms "antigen-binding fragment" and "antibody fragment" are interchangeable and refer to one or more antibody fragments that retain the ability to specifically bind to a target antigen. The antigen-binding function of an antibody can be performed by a fragment of a full-length antibody. An antibody fragment can be a Fab, F(ab')2, scFv, SMIP, diabody, triabody, affibody, nanobody, aptamer, or domain antibody. Examples of binding fragments encompassed by the term "antigen-binding fragment" of an antibody include, but are not limited to, (i) a Fab fragment, which is a monovalent fragment consisting of the VL, VH, CL, and CH1 domains; (ii) a F(ab)2 fragment, which is a bivalent fragment comprising two Fab fragments linked by a disulfide bond at the hinge region; (iii) an Fd fragment consisting of the VH and CH1 domains; (iv) an Fv fragment consisting of the VL and VH domains of a single arm of an antibody; (V) a dAb comprising the VH and VL domains; (vi) a dAb fragment consisting of the VH domain (Ward et al., Nature 341:544-546, 1989); (vii) a dAb consisting of a VH or VL domain; (viii) an isolated complementarity determining region (CDR); and (ix) a combination of two or more isolated CDRs, optionally linked by a synthetic linker. In addition, the two domains of the Fv fragment, VL and VH, are encoded by separate genes, but these two domains can be linked using recombinant techniques via a linker that can form a single protein chain (called single-chain Fv (scFv), see, for example, Bird et al. Science 242:423-426, 1988 and Huston et al., Proc. Natl. Acad. Sci USA 85:5879-5883, 1988) in which the VL and VH regions pair to form a monovalent molecule. These antibody fragments are obtained by conventional techniques known to those skilled in the art, and the fragments are screened for use in the same manner as intact antibodies. Antigen-binding fragments can be produced by recombinant DNA techniques, enzymatic or chemical cleavage of intact immunoglobulins, or in some embodiments, chemical peptide synthesis procedures known in the art.

[0020] As used herein, the term "complementarity determining region" (CDR) refers to the hypervariable regions found in both light and heavy chain variable domains. The more conserved parts of the variable domains are called framework regions (FR). As understood in the art, the amino acid positions that represent the hypervariable regions of an antibody can vary according to the context and the various definitions known in the art. Some positions in the variable domain can be considered hybrid hypervariable positions because these positions are considered to be within the hypervariable region in a set of standards (such as IMGT or KABAT) and outside the hypervariable region in a different set of standards (such as KABAT or IMGT). One or more of these positions can also be found in extended hypervariable regions. The present invention includes antibodies that contain modifications at these hybrid hypervariable positions. Naturally occurring heavy and light chain variable domains each contain four framework regions that adopt a predominantly lamellar structure linked by three CDRs (CDR1, CDR2, and CDR3) that form loops connecting and, in some cases, form part of the lamellar structure. The CDRs of each chain are held together by FR regions with the sequence FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4 and, together with the CDRs from the other antibody chain, contribute to the formation of the antigen-binding site of antibodies (see Kabat et al., Sequences of Proteins of Immunological Interest, National Institute of Health, Bethesda, Md. 1987, the contents of which are incorporated herein by reference). For example, as used herein, CDR1-VH, CDR2-VH, and CDR3-VH refer to the first, second, and third CDRs, respectively, of the heavy chain variable region (VH), where these three CDRs constitute a CDR combination of a heavy chain (or its variable region) (VH CDR combination), and CDR1-VL, CDR2-VL, and CDR3-VL refer to the first, second, and third CDRs, respectively, of the light chain variable region (VL), where these three CDRs constitute a CDR combination of a light chain (or its variable region) (VL CDR combination).

[0021] As used herein, the term "Kabat numbering system" generally refers to the immunoglobulin alignment and numbering system proposed by Elvin A. Kabat (see, e.g., Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md., 1991).

[0022] As used herein, the term "VH" refers to the variable region of an antibody's immunoglobulin heavy chain (including the heavy chain of an Fv, scFv, or Fab). The term "VL" refers to the variable region of an immunoglobulin light chain (including the light chain of an Fv, scFv, dsFv, or Fab). The term "heavy chain constant region" as used herein refers to the carboxy-terminal portion of an antibody heavy chain that is not directly involved in binding of an antibody to an antigen but exhibits effector functions such as interaction with an Fc receptor, and has a more conservative amino acid sequence compared to the variable domain of an antibody. The "heavy chain constant region" includes at least a CH1 domain, a hinge region, a CH2 domain, a CH3 domain, or a variant or fragment thereof. The "heavy chain constant region" includes a "full-length heavy chain constant region" and a "heavy chain constant region fragment", the former having a structure basically similar to that of a natural antibody constant region, and the latter including only a "part of a full-length heavy chain constant region". Exemplarily, a typical "full-length antibody heavy chain constant region" is composed of a CH1 domain-hinge region-CH2 domain-CH3 domain, and when the antibody is an IgE, it also includes a CH4 domain, and when the antibody is a heavy chain antibody, it does not include a CH1 domain. Exemplarily, a typical "heavy chain constant region fragment" may be selected from a CH1, Fc, or CH3 domain. The term "light chain constant region" as used herein refers to the carboxy-terminal portion of an antibody light chain that is not directly involved in the binding of an antibody to an antigen, said light chain constant region may be selected from a constant kappa domain or a constant lambda domain. The term "Fc" herein refers to the carboxy-terminal portion of an antibody obtained by papain hydrolysis of an intact antibody and typically includes the CH3 and CH2 domains of the antibody. Fc regions include, for example, native sequence Fc regions, recombinant Fc regions, and variant Fc regions. Although the boundaries of the Fc region of an immunoglobulin heavy chain can vary slightly, the Fc region of a human IgG heavy chain is usually defined to stretch from an amino acid residue at position Cys226, or from Pro230, to the carboxy-terminus thereof. Because the C-terminal lysine (based on residue 447 of the EU Kabat numbering system) of the Fc region can be removed, for example, during production or purification of the antibody, or by recombinant manipulations performed on a nucleic acid encoding an antibody heavy chain, the Fc region may or may not include Lys447.

[0023] As used herein, the terms "percent (%) sequence identity" and "percent (%) sequence identity" are interchangeable and refer to the percent of amino acid (or nucleotide) residues of a candidate sequence that are identical to the amino acid (or nucleotide) residues of a reference sequence after aligning the sequences to achieve maximum percent sequence identity and introducing gaps (if necessary) (e.g., for optimal alignment, gaps can be introduced in one or both of the candidate and reference sequences, and non-homologous sequences can be ignored for comparison purposes). For purposes of determining percent sequence identity, alignment can be achieved in a variety of ways well known to those of skill in the art, for example, using publicly available computer software such as BLAST, ALIGN, or Megalign (DNASTAIi) software. Those of skill in the art can determine appropriate parameters to be used for measuring alignment, including any algorithm required to achieve maximum alignment within the full length of the sequences being compared. For example, a reference sequence aligned for comparison with a candidate sequence can show that the candidate sequence exhibits 50% to 100% sequence identity over the entire length of the candidate sequence or a selected portion of consecutive amino acid (or nucleotide) residues of the candidate sequence. The length of the candidate sequence aligned for comparison purposes may, for example, be at least 30% (e.g., 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100%) of the length of the reference sequence. When a position in the candidate sequence is occupied by the same amino acid (or nucleotide) residue as the corresponding position in the reference sequence, then the molecules are identical at that position.

[0024] The term "conservative amino acids" as used herein generally refers to amino acids that belong to the same class or have similar characteristics (e.g., charge, side chain size, hydrophobicity, hydrophilicity, main chain conformation and rigidity, etc.) By way of example, the amino acids in each of the following groups belong to the conserved amino acid residues of each other, and substitutions of amino acid residues within the groups belong to the conserved amino acid substitutions. (1) Acidic amino acids: Asp (D) and Glu (E), (2) Basic amino acids: Lys (K), Arg (R) and His (H); (3) Hydrophilic uncharged amino acids: Ser (S), Thr (T), Asn (N) and Gln (Q); (4) aliphatic uncharged amino acids: Gly (G), Ala (A), Val (V), Leu (L) and Ile (I); (5) Nonpolar uncharged amino acids: Cys (C), Met (M) and Pro (P); (6) Aromatic amino acids: Phe (F), Tyr (Y) and Trp (W). As used herein, the term "specific binding" refers to a binding reaction that determines the presence of an antigen in a heterogeneous group of proteins and other biomolecules that are specifically recognized, for example, by an antibody or antigen-binding fragment thereof. An antibody or antigen-binding fragment thereof that specifically binds to an antigen binds to the antigen with a KD of less than 100 nM. For example, an antibody or antigen-binding fragment thereof that specifically binds to an antigen binds to the antigen with a KD of up to 100 nM (e.g., between 1 pM and 100 nM). An antibody or antigen-binding fragment thereof that does not exhibit specific binding to a particular antigen or epitope thereof exhibits a KD of greater than 100 nM (e.g., greater than 500 nM, 1 μM, 100 μM, 500 μM, or 1 mM) for that particular antigen or epitope thereof. Antibodies that specifically immunoreact with a particular protein or carbohydrate can be selected using a variety of immunoassays. For example, solid-phase ELISA immunoassays are routinely used to select antibodies that specifically immunoreact with a protein or carbohydrate. See Harlow & Lane, Antibodies, A Laboratory Manual, Cold Spring Harbor Press, New York (1988) and Harlow & Lane, Using Antibodies, A Laboratory Manual, Cold Spring Harbor Press, New York (1999), which describe immunoassays and conditions that can be used to determine specific immune reactivity.

[0025] As used herein, the term "multispecific antibody" refers to having at least two antigen-binding sites, each of which binds to a different epitope of the same antigen or a different epitope of a different antigen. Thus, terms such as "bispecific", "trispecific", "tetraspecific" and the like refer to the number of different epitopes to which an antibody / antigen-binding molecule can bind. The term "bispecific antibody" refers to an antibody, usually a human or humanized antibody, that has monoclonal binding specificity for at least two different antigens. In the present invention, one of the binding specificities can be detected against an antigenic epitope of TNFR2, and the other can be detected against another antigenic epitope of TNFR2 or any other antigen, such as a cell surface protein, a receptor, a receptor subunit, a tissue-specific antigen, a virus-derived protein, a virus-encoded envelope protein, a bacterial-derived protein or a bacterial surface protein. As used herein, the term "valency" refers to the presence of a given number of binding sites in an antibody / antigen-binding molecule. Thus, the terms "monovalent," "bivalent," "tetravalent," and "hexavalent" refer to the presence of one binding site, two binding sites, four binding sites, and six binding sites, respectively, in an antibody / antigen-binding molecule. As used herein, the term "humanized antibody" refers to a genetically engineered non-human antibody whose amino acid sequence has been modified to increase sequence homology with human antibodies. Generally speaking, all or part of the CDR regions of a humanized antibody are derived from a non-human antibody (donor antibody), and all or part of the non-CDR regions (e.g., variable region FR and / or constant region) are derived from a human immunoglobulin (acceptor antibody). A humanized antibody usually retains or partially retains the expected properties of the donor antibody, including, but not limited to, antigen specificity, affinity, reactivity, ability to enhance immune cell activity, ability to enhance immune response, etc. As used herein, the term "chimeric antibody" refers to an antibody having variable sequences derived from the immunoglobulin of one source organism (e.g., rat or mouse) and constant regions derived from the immunoglobulin of a different organism (e.g., human). Methods for producing chimeric antibodies are known in the art. See, e.g., Morrison, 1985, Science 229(4719):1202-7; Oi et al, 1986, BioTechniques 4:214-221; Gillies et al, 1985 J Immunol Methods 125:191-202, which are incorporated herein by reference. As used herein, the term "antibody conjugate" refers to a conjugate / complex formed by chemically binding an antibody molecule to another molecule, either directly or through a linker. The other molecule may be a therapeutic agent or a tracer, preferably, the therapeutic agent is selected from a radioisotope, a chemotherapeutic agent or an immunomodulatory agent, and the tracer is selected from a radiocontrast agent, a paramagnetic ion, a metal, a fluorescent label, a chemiluminescent label, an ultrasound contrast agent or a photosensitizer. An "antibody conjugate" is, for example, an antibody-drug conjugate (ADC) in which a drug molecule is the other molecule.

[0026] The term "antigen chimeric receptor (CAR)" herein refers to an artificial immune effector cell surface receptor that is engineered for expression on an immune effector cell and specifically binds to an antigen, and includes at least (1) an extracellular antigen-binding domain, such as a variable heavy or light chain of an antibody, (2) a transmembrane domain that anchors the CAR to the immune effector cell, and (3) an intracellular signaling domain. CARs can use the extracellular antigen-binding domain to redirect T cells and other immune effector cells to a selected target, such as a cancer cell, in an MHC-unrestricted manner. As used herein, the term "regulatory T cells" or "Tregs", also known as suppressor T cells, is a group of lymphocytes that negatively regulate the body's immune response to maintain tolerance to self-antigens, control excessive immune responses, avoid immune damage to normal cells, and prevent the occurrence of autoimmune diseases. Tregs express biomarkers CD4, FOXP3, and CD25, and are believed to be derived from the same lineage as naive CD47 cells. Tregs play a very important role in tumor development, and many studies have shown that the number of Treg cells in the tumor microenvironment is significantly increased in melanoma, ovarian cancer, breast cancer, colon cancer, lung cancer, pancreatic cancer, etc., and the number of Treg cells is closely related to the survival rate of tumor patients. In addition, tumor cells induce the proliferation of tumor-infiltrating Treg cells, and the proliferated Treg cells secrete large amounts of immunosuppressive factors such as TGF-β, which inhibit the function of immune cells such as CD8+ T cells and hinder the killing effect of immune cells against tumors, which is an important drug resistance mechanism that causes the failure of immunotherapy in many solid tumors and hematological tumors. Recent studies have shown that the immune tolerance of patients undergoing immunotherapy such as PD-1 / PD-L1 is also closely related to Tregs.

[0027] As used herein, the term "vector" includes nucleic acid vectors such as DNA vectors (such as plasmids), RNA vectors, and viruses or other suitable replicons (e.g., viral vectors). A variety of vectors have been developed for the delivery of polynucleotides encoding foreign proteins into prokaryotic or eukaryotic cells. Expression vectors of the invention include polynucleotide sequences and additional sequence elements, e.g., for protein expression and / or for integrating these polynucleotide sequences into the genome of mammalian cells. Particular vectors that can be used to express the antibodies and antibody fragments of the invention include plasmids that include regulatory sequences (such as promoter and enhancer regions) that direct the transcription of genes. Other useful vectors for expressing antibodies and antibody fragments include polynucleotide sequences that increase the translation rate of these genes or improve the stability or nuclear output of the mRNA produced by transcription of the genes. These sequence elements include, for example, 5' and 3' untranslated regions, internal ribosome entry sites (IRES), and polyadenylation signal sites to direct efficient transcription of genes carried in the expression vector. Expression vectors of the invention can also include a polynucleotide encoding a marker for selecting cells containing the vector. Examples of suitable markers include genes encoding resistance to antibiotics, such as ampicillin, chloramphenicol, kanamycin, or nourseothricin.

[0028] As used herein, the terms "subject," "subject" and "patient" refer to a living organism undergoing treatment for a particular disease or condition (e.g., cancer or an infectious disease) described herein. Examples of subjects and patients include mammals, such as humans, primates, pigs, goats, rabbits, hamsters, cats, dogs, guinea pigs, members of the bovine family (e.g., domestic cattle, bison, buffalo, elephant, yak, etc.), cows, sheep, horses, bison, etc., undergoing treatment for a disease or condition (e.g., a cell proliferative disease such as cancer or an infectious disease). As used herein, the term "treatment" refers to a surgical or therapeutic treatment aimed at preventing or slowing down (reducing) the progression of an undesirable physiological change or pathology in a subject, such as a cell proliferative disorder (such as cancer or an infectious disease). Beneficial or desired clinical results include, but are not limited to, relief of symptoms, reduction in the extent of disease, stable disease state (i.e., not worsening), delay or slowing of disease progression, improvement or mitigation of disease state, and remission (whether partial or total remission), whether detectable or undetectable. Subjects in need of treatment include those already suffering from a disease or disorder, and those susceptible to a disease or disorder, or those in whom a disease or disorder is to be prevented. When referring to terms such as slowing, alleviation, reduction, mitigation, remission, and the like, conditions such as resolution, disappearance, non-occurrence, and the like are also included. As used herein, the term "effective amount" refers to an amount of a therapeutic agent that is effective to prevent or ameliorate the symptoms of a disease or the progression of the disease when administered alone or in combination with another therapeutic agent to a cell, tissue, or subject. "Effective amount" also refers to an amount of a compound that is sufficient to ameliorate a symptom, e.g., treat, cure, prevent, or ameliorate an associated medical condition, or treat, cure, prevent, or ameliorate an increase in the rate of such a condition. When an active ingredient is administered alone to an individual, the therapeutically effective dose is the amount of that ingredient alone. When a combination is used, the therapeutically effective dose refers to the combined dose of the active ingredients that produces a therapeutic effect, regardless of combined, sequential, or simultaneous administration. EXAMPLES

[0029] The present invention will be further described below with reference to specific examples, and the advantages and features of the present invention will become clear as the description proceeds. If specific conditions are not specified in the examples, general conditions or conditions recommended by the manufacturer are used. If the manufacturer of the reagents or equipment used is not specified, they may be general products available on the market. The embodiments of the present invention are merely illustrative and do not limit the scope of the present invention. Without departing from the spirit and scope of the present invention, the details and forms of the technical solutions of the present invention may be modified or replaced, but it should be understood by those skilled in the art that all such modifications and replacements are within the protection scope of the present invention.

[0030] Example 1 Expression and purification of anti-TNFR2 humanized monoclonal antibodies 1.1 Humanization of anti-TNFR2 antibodies The antibody was humanized using the "CDRs grafting" method, that is, the most homologous human antibody was selected based on the sequence to provide the antibody framework region (FRs), and the complementarity determining regions (CDRs) of the antigen-binding fragment of the target antibody based on the Kabat nomenclature were grafted onto the former to form a humanized antibody variable region sequence of the sequence FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4. Then, in order to effectively maintain the activity and affinity of the antibody, potential back-mutation points were selected based on the antibody structure modeling (MOE software) with the following selection criteria: 1) amino acid residues in the antibody framework region located at the VH-VL interface, which are close to the CDRs or directly interact with the CDRs, were selected for back-mutation, and such amino acid residues are relatively important for maintaining the conformation of the CDRs region; 2) amino acids embedded in the protein were selected as much as possible for back-mutation in consideration of immunogenicity; and 3) mutations with reduced molecular energy are preferred in consideration of the stability and expression level of the antibody. Humanized antibodies with affinity, antibody characterization, and activity function comparable to or better than those of the murine antibodies were screened by testing humanized antibodies containing different mutations for affinity to human TNFR2 and binding to cells expressing TNFR2 on their surface. Among them, the complementarity determining regions (CDRs) of the antigen-binding fragment of the TNFR2 antibody according to the Kabat nomenclature are shown in Table 1, Table 2 shows the VH and VL sequences of the humanized antibody molecule, and Table 3 shows the pairing situation of the VH and VL sequences of the humanized anti-TNFR2 antibody.

[0031] [Table 1]

[0032] [Table 2] TIFF0007635401000003.tif251170

[0033] [Table 3]

[0034] 1.2 Expression of anti-TNFR2 humanized antibodies The day before transfection, count ExpiCHO-S cells and dilute them at 2.5–4 (10 6 The cells were inoculated into freshly prewarmed ExpiCHO expression medium (Invitrogen, A291002) at a density of 100 cells / mL and cultured overnight. On the day of transfection, the overnight cultured ExpiCHO-S cell suspension was counted, revealing a cell concentration of approximately 7–10 (10 6 The number of cells was 1000 cells / mL and the cell viability for transfection was greater than 95%. Depending on the number of transfections, take the required number of cells and dilute them in ExpiCHO expression medium to a final concentration of 6 (10 6 The plasmids were diluted to 100 cells / mL and placed on a shaker at 37°C, 8% CO2, 100 rpm for later use. TM Dilute with SFM medium (Invitrogen, 12309019) and mix well by gently shaking the centrifuge tube. TM CHO reagent (Invitrogen, A29129) was added to the plasmid dilution solution, the centrifuge tube was gently shaken to mix well, and the tube was left to stand at room temperature for 2 minutes. TMThe CHO reagent complex was slowly added dropwise to the cell suspension to be transfected, and the flask was shaken during the addition. After transfection, the transfected cells were cultured at 37°C, 8% CO2, and 100 rpm in a shaker. One day after transfection, the transfected cells were treated with 0.6% ExpiFectamine. TM CHO Enhancer (Invitrogen, A29129) and 16% ExpiCHO TM Feed (Invitrogen, A29129) was added, the flask was gently shaken during the addition, and the cells were transferred to a shaker at 32°C, 5% CO2, 100 rpm and cultured. Five days after transfection, the transfected cells were added with 16% ExpiCHO TM Feed was added and the flask was gently shaken during the addition. On the 12th day after transfection, the cell supernatant was collected and centrifuged at 4000 g for 10 minutes, and the supernatant was aspirated to further purify the antibody.

[0035] 1.3 Purification of anti-TNFR2 humanized antibody The cell culture supernatant collected by high-speed centrifugation was filtered through a 0.45 + 0.22 (M) membrane filter, and the first step of purification was performed by affinity chromatography using Akta Avant 150 (Cytiva). The chromatography medium was Mabselect PrismA (Cytiva, catalog number: 17549803), a Protein A filler that interacts with Fc, and the equilibration buffer was PBS (2.5 g / L Na2HPO4 12H2O, 0.408 g / L NaH2PO4, 8.76 g / L NaCl, pH 7.2). After equilibration to 4 times the column volume, the cell supernatant was loaded and bound, and the flow rate was controlled so that the sample was retained on the column for 5 min or more. After loading, the column was washed with PBS (pH 7.2) until the ultraviolet absorption of A280 decreased to the baseline. Next, the column was washed with 20 mM PB + 1 M NaCl (3.752 g / L The column was rinsed with 2x column volume of PBS (pH 7.2) (Na2HPO4·12H2O, 1.314 g / L NaH2PO4, 58.44 g / L NaCl pH 6.2). The column was further washed with PBS (pH 7.2) until the A280 UV absorption and conductance reached baseline. Finally, the chromatography column was washed with elution buffer of 20 mM citric acid (2.184 g / L citric acid, 1.086 g / L sodium citrate, pH 3.4), the elution peak was collected according to the A280 UV absorption peak, and the collected elution sample was neutralized with 1 M Tris (121.14 g / L Tris) and detected to neutrality with a pH meter Seven2Go (Mettler-Toledo). The collected antibody was identified to be more than 95% pure by SEC-HPLC and used for subsequent studies.

[0036] Example 2 Detection of specific binding of TNFR2 humanized antibodies to human and cynomolgus monkey TNFR2 proteins by ELISA Human TNFR2 (Human TNFR2-His, Sino 10417-H08H) or cynomolgus TNFR2 (Cynomolgus TNFR2-His, Sino 90102-C08H) was pre-encapsulated in an ELISA plate at 100 μL / well and 0.5 μg / mL, and a test anti-TNFR2 humanized antibody (constructed by linking the variable region described in Example 1 to IgG-Fc, and the WT chimeric antibody also has an IgG-Fc structure) was serially diluted 3.33-fold and added at 100 μL / well, and incubated at room temperature with shaking for 1.5 hours. After washing the plate, mouse anti-human IgG was added. Fc-HRP standard solution (1:10000 dilution) was added, 100 μL / well, and incubated at room temperature with shaking for 1.0 hour, the plate was washed again, HRP substrate TMB was added to develop color, stop solution was added to stop the reaction, and absorbance was read with a microplate reader (MD I3). The antibody binding curve was plotted with antibody concentration on the horizontal axis and corresponding OD value on the vertical axis, and 4-parameter fitting (GraphPad Prism9) was performed to calculate the EC50 value. The smaller the EC50 value, the stronger the antibody's ability to bind to human / cynomolgus TNFR2. The binding effect of the humanized antibody was normalized to the corresponding human-mouse chimeric antibody WT (see SEQ ID NOs: 38-43 for the sequence), and the higher the percentage value, the better the binding effect of the humanized antibody. The binding results of the anti-TNFR2 antibody with human TNFR2 protein are shown in Figure 1 and Table 4, and the binding results with cynomolgus TNFR2 are shown in Figure 2 and Table 4. The data show that all the tested antibodies can specifically bind to human or monkey TNFR2 protein, and the binding ability of the humanized antibodies is essentially the same as that of the human-mouse chimeric antibody.

[0037] [Table 4]

[0038] 001-WT VH amino acid sequence (SEQ ID NO:38): EVQLQESGGGLVQPGGSLNLSCAASGFAFSTYDLSWVRQTPEKRLEWVAYINNGGISTYYSDTVKGRFTISRDNAKNTLYLQMSSLKSEDTAMYYCVRGPFYGSANYFDYWGQGTTVTVSS 001-WT VL amino acid sequence (SEQ ID NO:39): EIVMTQSPASLSLSVGETVTITCRTSESIYSNLPWYQQKQGKSPQLLVYDATKLAEGVPSRFSGSESGTQYSLKINSLQSEDFGTYYCQHFWVTPWTFGGGTKLEIK 219-WT VH amino acid sequence (SEQ ID NO:40): EVQLQESGAELVRPGASVKLSCKASGYSFTNYWMNWVKQRPGQGLEWIGMIHPSDTETRLNQNFKDKATLTVDKSSSTSYMQLSSPTSEDSAVYYCARGEGLGAARSVSMDYWGQGTTVTVSS 219-WT VL amino acid sequence (SEQ ID NO:41): DILMTQSPSSLSASLGDRVTISCRASQDISNYLNWYQQKPDGTVKVLIYYTAILHSGVPSRFSGSGSGTDYSLTISNLEQEDIATYFCQQGNTLPWTFGGGTKLEIK 224-WT VH amino acid sequence (SEQ ID NO:42): EVQLQESGPEIVKPGASVKLSCTASGFNNKDIYMHWVKQRPEQGLEWIGRIDPATGNTKHDPKFQDKATLSSDTSSNTAYLQFSSLTSEDTAVYYCAHSPYGDFGAMDYWGQGTTVTVSS 224-WT VL amino acid sequence (SEQ ID NO:43): DIQMTQSPAIMSASLGERVTMTCTASSSVSSNYLHWYQQKPGSSPKLWIYSTSNLPSGVPARFSGSGSGTSYSLTISSMEAEDAATYYCHQYHRSPWTFGGGTKLEIK

[0039] Example 3: Detection of affinity between TNFR2 humanized antibodies and human and cynomolgus monkey TNFR2 proteins by BIAcore The specific binding of the test anti-TNFR2 antibodies to human and cynomolgus TNFR2 proteins was detected by BIAcore. The experiment used a Protein A chip, and the time required for the chip to capture the diluted antibody was measured in a manual run so that the Rmax, which can saturate the bound antigen, was 50 RU. Both human (Human TNFR2-His, Sino 10417-H08H) and cynomolgus (Cynomolgus TNFR2-His, Sino 90102-C08H) TNFR2 were serially diluted to 32, 16, 8, 4, and 2 nM. The affinity of the antibody to the antigen was measured using multi-cycle kinetics. In each cycle, the antibody was injected, followed by the injection of TNFR2 protein at gradient concentrations, allowing the binding and dissociation process of the antigen and antibody to occur. After each cycle, the Protein A chip was regenerated (removing the proteins on the chip) using Glycine pH 1.5. The antibody-antigen affinity KD was fitted using BIAcore T200 analysis software. The results in Table 5 show that all tested anti-TNFR2 antibodies have specific binding to human or cynomolgus TNFR2 protein, and the affinity level is relatively high.

[0040] [Table 5]

[0041] Example 4 Detection of binding of TNFR2 antibodies to human TNFR2 on CHO-TNFR2 cells by FACS We took CHO-K1 stable cells transfected with human TNFR2 high expression plasmid (named CHO-TNFR2), the transfected human TNFR2 full-length plasmid was purchased from Sino Biological (Catalog No.: HG10417-UT, NCBI Ref Seq: NM_001066.2), and performed experiments when the cell density was not higher than 80%. Discard the cell medium, wash with PBS, add 1mL trypsin to digest for 2 minutes, and stop the digestion with Ham's F12 complete medium containing 10% FBS to make a cell suspension. After counting, take an appropriate amount of cell suspension, centrifuge at 350 × g, discard the supernatant, and extract 1 × 10 7 The cells were resuspended by adding a corresponding amount of blocking solution (10% FBS + PBS) at a density of 10 cells / mL and incubated at 4 °C for 30 min. After incubation, the cells were centrifuged at 350 × g to remove the supernatant, and the cells were resuspended in 2 × 10 6The cells were resuspended to a density of 1000 cells / mL and spread into a 96-well plate, and 50 μL of cell suspension was added to each well for later use. Antibodies were serially diluted 10-fold using PBS, starting from the highest concentration of 20 μg / mL (2x concentration), and the diluted antibodies were added to the wells already containing 50 μL of cell suspension, placed on a microplate shaker, shaken at 500 rpm for 1 min to thoroughly mix the antibody and cells, and incubated at 4°C for 1 h. After the incubation was completed, the cells were washed twice with 100 μL / well of staining buffer, centrifuged at 350 × g for 5 min, and the supernatant was discarded. PE goat anti-Human IgG Fc antibody (ebioscience, Cat. No.: 12-4998-82) was diluted 250-fold in staining buffer, added to the washed cell wells in a volume of 100 μL per well, mixed well, and stained for 30 min at 4°C. After staining, the cells were washed twice with staining buffer in the same manner, and finally, the cells were resuspended in 200 μL of staining buffer, and the signal was detected by a flow cytometer (Thermo Attune NxT). The stronger the signal, the stronger the binding ability of the antibody to TNFR2. The antibody binding curve was plotted with the antibody concentration on the horizontal axis and the corresponding multiple of the mean fluorescence intensity (MFI) on the vertical axis, and 4-parameter fitting (GraphPad Prism9) was performed to calculate the EC50 value. The smaller the EC50 value, the stronger the antibody's ability to bind to CHO-TNFR2 cells. The binding effect of the humanized antibody was normalized to the corresponding human-mouse chimeric WT antibody, and the higher the percentage value, the better the binding effect of the humanized antibody. As shown in Figure 3 and Table 6, all tested anti-TNFR2 antibodies can bind to human TNFR2 on the CHO-TNFR2 cell surface, and the binding ability of the humanized antibody is basically the same as that of the human-mouse chimeric WT antibody.

[0042] [Table 6]

[0043] Example 5: Detection experiment of binding between antibody and TNFR2 on the surface of human regulatory T cells (Treg cells) by FACS Human Treg cells were isolated from human PBMCs using a sorting kit (Stemcell, Catalog No.: 18063), stimulated and expanded in vitro for 15 days using Dynabeads Human Treg Expander (Gibco, Catalog No.: 11129D), and then individually packaged and cryopreserved. The in vitro isolated and expanded Treg cells were taken and allowed to recover overnight, centrifuged the next day at 300 × g for 5 min, resuspended in DPBS to obtain a cell suspension, and counted. The number of cells required for the experiment was placed in a centrifuge tube, centrifuged at 300 × g for 5 min, the supernatant was removed, and the cell density was adjusted to 2 × 10 in staining buffer. 6 The plate was adjusted to 200ng / mL and spread at 50μL per well on a 96-well plate. All test antibodies and the control antibody anti-Hel isotype (each diluted to 200ng / mL with PBS, total volume 100μL) were taken. Each sample was added to each well at 50μL / well. The plate with the cell suspension and antibody added was placed on a microplate shaker and shaken at 500rpm for 1min to thoroughly mix the cells and antibodies. After mixing, the plate was placed in a 4℃ refrigerator and incubated for 60min. After the incubation was completed, 100μL of staining buffer was added to each well, centrifuged at 350×g for 5min, the supernatant was discarded, and 200μL of staining buffer was added to each well to resuspend the cells, centrifuged at 350×g for 5min, and the supernatant was discarded. The staining buffer was added to PE goat anti-Human IgG Fc at a ratio of 250:1 (staining buffer: fluorescent staining antibody) to make the staining solution, which was mixed well and added to the cell wells at 100 μL per well, and the plate was placed on a microplate shaker and shaken at a speed of 500 rpm for 1 min to thoroughly mix the cells and the staining solution. After mixing, the plate was placed in a 4°C refrigerator and incubated for 30 min. The cells were washed twice, and finally 200 μL of PBS was added to each well to resuspend the cells, and the signals were detected by a flow cytometer (Thermo Attune NxT). Figure 4 shows that all anti-TNFR2 humanized antibodies can effectively bind to human Treg cells.

[0044] Example 6: Detection of binding between antibodies and activated cynomolgus monkey PBMC cells by FACS After the cryopreserved cynomolgus monkey PMBC cells were recovered, they were resuspended in complete medium (RPMI1640-Glutamax+10%FBS+1xP / S+1xITS+50μM PM mercaptoethanol) to obtain a cell suspension and counted. According to the counting results, the cells were diluted to 5x10 6 The cells were resuspended to a density of 100 µL / mL and spread in a 96-well U-bottom plate at 100 µL per well. A 20% concentration of T cell activation reagent, Immunocult T cell (Stemcell, 1:50) activator + rhIL-2 (R&D, 200 IU), was prepared and the 20% concentration of the activation reagent was added to the cells at 100 µL per well, mixed well and cultured in a 37°C, 5% CO2 incubator for 3 days. The activated cells were collected and counted, and the cell density was adjusted to 4 × 10 using staining buffer (DPBS solution containing 2% FBS). 6The antibody was adjusted to 0.4μg / mL and spread at 50μL per well on a 96-well V-bottom plate. All test antibodies and anti-Hel control antibodies (diluted to 0.4μg / mL and 4μg / mL in staining buffer, respectively) were taken and each sample was added to each well at 50μL / well. The plate with the cell suspension and antibody added was placed on a microplate shaker and shaken at 500rpm for 1min to thoroughly mix the cells and antibodies. After mixing, the plate was placed in a 4℃ refrigerator and incubated for 30min. After the incubation was completed, 100μL of staining buffer was added to each well, centrifuged at 350×g for 5min, the supernatant was discarded, and 200μL of staining buffer was added to each well to resuspend the cells, centrifuged at 350×g for 5min, and the supernatant was discarded. Antibody Anti-Human CD8-FTIC (BD-555366, 1 μL / test) and PE goat anti-Human IgG Fc (Invitrogen-124998-82, 0.5 μL / test) were added, and the plate was placed on a microplate shaker and shaken at a speed of 500 rpm for 1 min to thoroughly mix the cells and staining solution. After mixing, the plate was placed in a 4°C refrigerator and incubated for 30 min. The cells were washed twice, and finally 200 μL of staining buffer was added to each well to resuspend the cells, and the signal was detected by a flow cytometer (Thermo Attune NxT). Figure 5 shows that the anti-Hel negative isotype control antibody did not bind to cynomolgus monkey CD8 T cells, and all tested anti-TNFR2 humanized antibodies could effectively bind to CD8+ T cells in activated cynomolgus monkey PBMCs.

[0045] Example 7: Detection of anti-TNFR2 antibodies blocking the binding of TNFα to TNFR2 by ELISA Human TNFR2 (Novoprotein, Catalog No. C830) was pre-coated on an ELISA plate at 100 μL / well, 1 μg / mL. All test TNFR2 antibodies were serially diluted 2.5-fold from the highest concentration of 30 μg / mL. The diluted antibodies were mixed with 15 ng / mL human TNFα-Biotin (Acro Biosystem, Catalog No. TNA-H82E3) in equal amounts, added to the ELISA plate at 100 μL / well, and incubated at room temperature for 2.0 hours with shaking. After washing the plate, Streptavidin-HRP standard solution (1:10000 dilution) was added at 100 μL / well and incubated at room temperature for 40 minutes with shaking. The plate was washed again, and TMB, a substrate for HRP, was added to develop color, and the reaction was stopped by adding a stop solution, and the absorbance was read using a microplate reader (MD I3). The antibody inhibition curves were plotted with the antibody concentration on the horizontal axis and the corresponding OD value on the vertical axis, and 4-parameter fitting (GraphPad Prism9) was performed to calculate the IC50 value. The smaller the IC50 value, the stronger the antibody's ability to inhibit the binding of human TNFα and human TNFR2. The blocking effect of the humanized antibody was normalized to the corresponding human-mouse chimeric antibody WT, and the higher the percentage value, the better the inhibitory effect of the humanized antibody. The blocking curves of the tested antibodies are shown in Figure 6, and the inhibitory activity is shown in Table 7. From Figure 6 and Table 7, it can be seen that all the tested antibodies can significantly inhibit the binding of human TNFα and human TNFR2 protein, and the inhibitory ability of the humanized antibodies is basically the same as that of the human-mouse chimeric WT antibody.

[0046] [Table 7]

[0047] Example 8 Anti-TNFR2 antibodies block the binding of TNFR2 to TNFα on CHO cells highly expressing human TNFR2 The experiment was carried out using CHO stable cells (same as CHO-TNFR2 in Example 4) that highly express human TNFR2. After digestion, the CHO-TNFR2 cells were washed twice with DPBS and stained with Live / Dead (L / D) (20 min at room temperature), and then 1 × 10 5 Cells were spread on the plate at 50 μL / well, and the test anti-TNFR2 antibody was diluted to 6 μg / mL in staining buffer as the initial concentration, and then serially diluted 3.33-fold to set a total of 7 concentration points. The diluted antibody was added to the plated cells at 50 μL / well, gently mixed and incubated at 4 °C for 30 minutes. Then, human TNFα-biotin diluted to 100 ng / mL was added at 100 μL / well, gently mixed and incubated at 4 °C for 30 minutes. After washing twice with staining buffer, PE-streptavidin (BioLegend, Cat. No. 405204) was added at 100 μL / well, 0.12 μg / mL, and incubated at 4 °C for 30 minutes. After washing twice with staining buffer, the cells were resuspended in 150 μL and detected by a flow cytometer (Thermo Attune NxT). The antibody inhibition curves were plotted with the antibody concentration on the horizontal axis and the corresponding MFI value on the vertical axis, and 4-parameter fitting (GraphPad Prism9) was performed to calculate the IC50 value. The smaller the IC50 value, the stronger the ability of the antibody to inhibit the binding of human TNFα to human TNFR2. The blocking effect of the humanized antibody was normalized to the corresponding human-mouse chimeric WT antibody, and the higher the percentage value, the better the inhibitory effect of the humanized antibody. The blocking curves of the tested antibodies are shown in Figure 7, and the inhibitory activity is shown in Table 8. From Figure 7 and Table 8, it can be seen that all the tested antibodies can significantly inhibit the binding of TNFα to TNFR2 on CHO-TNFR2 cells.

[0048] [Table 8]

[0049] Example 9: FACS detection experiment of antibody inhibition of TNF-induced human Treg cell IκBα degradation Human Treg cells were isolated from human PBMCs using a sorting kit (Stemcell, Catalog No.: 18063), stimulated and expanded in vitro for 15 days with Dynabeads Human Treg Expander (Gibco, Catalog No.: 11129D), then individually packaged and cryopreserved. The in vitro isolated and expanded Treg cells were taken, recovered overnight, centrifuged at 300 × g for 5 minutes the next day, cultured in AIM-V medium (brand Gibco, Catalog No. 31035025) and counted, and the cell density was adjusted to 6 × 10 according to the cell counting results. 6The antibody was adjusted to cells / mL and spread at 25μL per well on a 96-well plate. All test antibodies and anti-Hel control antibodies were taken (diluted to 40% concentration with AIM-V medium to 1μg / mL, 10μg / mL, and 100μg / mL, respectively). Each concentration of antibody was added to the corresponding cell well at 25μL per well. After mixing with a multichannel pipette, the wells were placed in a 37℃, 5% CO2 incubator and pre-incubated for 30min. TNFα (brand Novoprotein, catalog number C008) was diluted to 20ng / mL, which is twice the working concentration, using AIM-V medium, and 50μL of TNFα was added to wells requiring TNFα activation and 50μL of AIM-V medium to non-activated control wells so that the final concentration of antibody was 1x and the final concentration of TNFα was 10ng / mL, and the plates were mixed with a pipette and incubated in a 37°C incubator for 10min. After incubation, the plates were removed, 100μL of pre-chilled DPBS was added, and the plates were centrifuged at 4°C and 300g for 5min. Next, the cells were reacted on ice for 20min using 100μL of 1x live / dead violet (diluted 500x with pre-chilled DPBS). 100μL of staining buffer was added to each well and centrifuged at 4°C and 300g for 5min. 100μL of 1x fix-perm buffer (Brand BD, Catalog No. 554714) was added to each well, mixed well, and fixed at 4℃ for 30min. After fixation, 100μL of 1x perm buffer was added to each well to stop fixation, centrifuged at 400g for 5min, and the supernatant was discarded. Next, 200μL of 1x perm buffer was added to each well to wash the cells twice. 100μL of IκBα staining solution (diluted 100 times with 1x perm buffer) was added to the experimental wells, and 1μL of Rat IgG2b kappa Isotype Control antibody was added to the control wells, mixed well, and incubated at 4℃ for 30min. After incubation, 100μL of 1x perm buffer was added to each well to stop fixation, centrifuged at 400g for 5min, and the supernatant was discarded. Next, 200μL of 1x perm buffer was added to each well to wash the cells twice.Detection was performed using a flow cytometer (Thermo Attune NxT). IκBα in live cells. low The MFI of IκBα in the percent or total viable cells was analyzed by flow cytometry. low The lower the ratio, the stronger the ability of the anti-TNFR2 antibody to inhibit TNFα-induced IκBα degradation. The results in Figure 8 show that the negative control antibody anti-Hel has no effect on the expression of IκBα, but all of the tested anti-TNFR2 humanized antibodies can inhibit TNFα-induced IκBα degradation.

[0050] Example 10 Inhibition of TNFR2 antibodies against TNFα and IL-2-induced Treg cell proliferation The inhibitory effect of this antibody on TNFα- and IL-2-induced Treg cell proliferation was determined by measuring the proliferation of TNFα- and IL-2-induced Treg cells in the presence of TNFR2 antibody (Zaragoza B et al., Nat Med. 2016 Jan;22(1):16-7). In vitro proliferation. Isolated and cryopreserved Treg cells were taken, allowed to recover overnight, centrifuged the next day at 400×g for 5 minutes, resuspended in medium to obtain a cell suspension, and counted. Tregs were stained with CellTrace Violet cell proliferation kit (Thermo Cat. No. C34557) and cultured at 1×10 7 1 mL of staining solution was prepared using 1 μL of stock solution per cell. Staining was performed at 37°C for 20 min, the reaction was neutralized with at least 5 volumes of complete medium, left to stand for 5 min, and centrifuged at 400 × g for 5 min. Cells were washed once by resuspending in medium, centrifuged again, and the supernatant was removed. 1 × 10 cells were stained per well of a 96-well plate. 5 Spread cells at a density of 1 x 10 5The cells were resuspended at a density of 50 μL of medium per cell and transferred to a 96-well plate. 50 μL of the test antibody was added to each well so that the final concentration of the antibody was 12.5 μg / mL, and incubated in an incubator for 30 min. Then, 50 μL of medium containing IL-2 (final concentration 300 IU) and TNFα (final concentration 50 ng / mL) and 50 μL of medium containing anti-CD3 / CD28 Dynabeads (Gibco, Catalog No.: 11129D, beads / Treg cell ratio 1:20) were added to each well, making the final volume of each well 200 μL. Two parallel wells were set up for each condition, and the plates were mixed and cultured in a 37°C incubator for 3 days for FACS detection (Thermo Attune NxT). The inhibitory effect of the antibody on TNFα- and IL-2-induced Treg proliferation was determined by the percentage of Treg proliferation. The results are shown in FIG. 9. Compared with the control anti-Hel antibody, all of the anti-TNFR2 humanized antibodies were able to effectively inhibit the proliferation of TNFα- and IL-2-induced Treg cells, and the differences were significant.

[0051] Example 11 Inhibition of anti-TNFR2 antibodies on Treg function The inhibitory effect of the antibody on the inhibitory function of Treg cells was determined by measuring the inhibitory function of Treg cells against effector (responder) T cells under conditions containing anti-TNFR2 antibody. Treg (CD4+CD25+FoxP3+T cells) and conventional T cell (Tcon) effector cells (CD4+CD25-T cells) required for the experiment were taken, recovered overnight, centrifuged at 400 × g for 5 minutes the next day, resuspended in complete medium (RPMI1640-Glutamax+10%FBS+1×P / S+1×ITS+50μM PM mercaptoethanol) to obtain a cell suspension, and counted. Tcon cells were stained with CellTrace Violet cell proliferation kit (Thermo Cat. No. C34557) and cultured at 1 × 10 71 mL of staining solution was prepared using 1 μL of stock solution per cell. Staining was performed at 37°C for 20 min, the reaction was neutralized with at least 5 volumes of complete medium, left to stand for 5 min, and centrifuged at 400 × g for 5 min. Cells were washed once by resuspending in medium, centrifuged again, and the supernatant was discarded. 1 × 10 cells were stained per well of a 96-well plate. 5 Spread cells at a density of 1 x 10 5 The cells were resuspended at a density of 50 μL of medium per cell and transferred to a 50 mL centrifuge tube. At the same time, Treg cells were prepared and co-cultured with Tcon cells at a ratio of 1:1. According to the number of Tcon cells, the corresponding anti-CD3 / CD28 Dynabeads (Gibco, Cat. No.: 11129D) were prepared at a ratio of 1 / 10. They were added to the Treg and Tcon medium at a volume of 50 μL per well. The test antibody was added to each well so that the final concentration of the antibody was 12.5 μg / mL. Three parallel wells were set up for each condition, and the plate was mixed and cultured in a 37°C incubator for 4 days and detected by flow cytometer. The higher the percentage of Tcon proliferation, the stronger the ability of the antibody to inhibit Treg. The inhibition results are shown in FIG. 10. All three tested anti-TNFR2 humanized antibodies could significantly inhibit the inhibitory effect of Treg on Tcon cells and promote the proliferation of Tcon, with statistical differences.

[0052] Example 12 Detection of Anti-TNFR2 Antibody-Mediated Antibody-Dependent Cellular Cytotoxicity (ADCC) Activity by FACS PBMCs and cryopreserved Treg cells were cultured in complete medium (RPMI1640-Glutamax+10%FBS+1xP / S+1xITS+50μM PM mercaptoethanol) 1 day prior, of which PBMCs were supplemented with 100IU / mL IL-2. On the day of the experiment, NK cells were isolated from PBMCs according to the requirements of the isolation kit (Stemcell, Cat. No. 17955) and cultured at 0.8x10 in complete medium (without IL-2). 6 The target cells, Treg cells or CHO-TNFR2 cells, were labeled with Cell Trace violet reagent and resuspended at a density of 0.4 × 10 6The antibody was adjusted to 100 μL / mL. The test antibody was serially diluted in complete medium to 4 times the final concentration for later use. Target cells were seeded on the cell plate at 50 μL per well according to the distribution diagram of the experimental plate, and the diluted drug was spread into the corresponding wells and incubated with the target cells at 37 °C for 30 minutes. After the incubation, 100 μL of effector cell suspension was added to the wells that needed to add effector cells, and 100 μL of medium was replenished to the wells that did not need to add effector cells, and incubated at 37 °C for 4 h. After the reaction, 1 μL of PI dye was added to each well and detected by the instrument. The higher the percentage of PI positive in the target cells, the more significant the ADCC effect. The results of the ADCC experiment are shown in Figure 11. The anti-Hel negative control antibody had no target and therefore no ADCC killing effect, and the three test humanized antibodies all showed ADCC activity in both target cells, Treg and CHO-TNFR2 cells.

[0053] Example 13 Detection of hTNFR2 and mTNFR2 Expression in TNFR2 Transgenic Humanized Mice (TNFR2 HuGEMM) In collaboration with Zhongmei Crown Biotechnology Co., Ltd., we used CRISPR / Cas9 technology to knock-in the hTNFRSF1B-WPRE-PA expression frame into the exon 2 site of the Tnfrsf1b gene by homologous recombination, obtaining heterozygous BALB / c mice in which the Tnfrsf1b gene was knocked into hTNFRSF1B-WPRE-PA, and then bred them to obtain homozygous transgenic mice expressing the human Tnfrsf1b (TNFR2) gene (TNFR2 HuGEMM). Peripheral blood was collected from 6-8 week-old female BALB / c mice (from Beijing Weitong Lihua Laboratory Animal Technology Co., Ltd.) and TNFR2 HuGEMM mice, red blood cells were removed using ACK (Gibco, Cat. No. A1049201), and FACS immunophenotyping was performed to detect the expression of mTNFR2 and hTNFR2 in CD4+T cells, CD8+T cells, and CD4+CD25+Foxp3+Treg cells in mouse peripheral blood, and all cell populations were gated based on FMO control (Figure 12A). The results showed that TNFR2 HuGEMM mice did not express mTNFR2, and the expression profile / expression level of hTNFR2 on the surface of CD4+T cells, CD8+T cells, and Treg cells was consistent with mTNFR2 in BALB / c background mice, indicating that TNFR2 HuGEMM mice had completed the replacement of mTNFR2 with hTNFR2 (Figure 12B-12C).

[0054] Example 14. Inhibition of anti-TNFR2 antibodies on TNFα-induced Treg cell proliferation in TNFR2 HuGEMM By measuring TNFα-induced Treg cell proliferation in TNFR2 HuGEMM mice in the presence of TNFR2 antibodies, it was confirmed that the TNFR2 signaling pathway and corresponding functions were preserved in the genetically modified TNFR2 HuGEMM mice, ensuring that the modified transgenic mice could be used for in vivo efficacy evaluation of candidate anti-TNFR2 antibodies. Five TNFR2 HuGEMM mice and five wild-type Balb / c mice were prepared, and the mouse spleens were aseptically removed and crushed in a safety cabinet. All the crushed cell suspensions were transferred to 15 mL centrifuge tubes and centrifuged (320 g, 7 min, 4 °C). The supernatant was discarded. Approximately 2-3 mL of ACK red blood cell lysis buffer (Gibco, catalog number A1049201) was added and mixed well, and the mixture was left at room temperature for 3-5 min until the red blood cells were completely lysed, and 6-8 mL of RPMI1640 medium was added to stop the lysis, and the mixture was inverted and mixed well. The mixture was centrifuged (200 g, 8 min, 4 °C). After centrifugation, the supernatant was discarded, the cells were resuspended in EasySep buffer, filtered through a 40 μm membrane filter, and counted. Treg cells were then selected according to the instructions of the Mouse CD4+CD25+Regulatory T kit (Stemcell brand, catalog number 18783A). The selected Treg cells were stained with CellTrace Violet cell proliferation kit (Thermo catalog number C34557) and 1 × 10 7 1 mL of staining solution was prepared using 1 μL of stock solution per cell. Staining was performed at 37°C for 20 min, the reaction was neutralized with at least 5 volumes of complete medium, left to stand for 5 min, and centrifuged at 400 × g for 5 min. Cells were washed once by resuspending in medium, centrifuged again, and the supernatant was removed. 1 × 10 cells were stained per well of a 96-well plate. 5 Spread cells at a density of 1 x 10 5The cells were resuspended at a density of 50 μL of medium per cell and transferred to a 96-well plate. 50 μL of test antibodies (including three humanized TNFR2 antibodies, one anti-mouse TNFR2 replacement antibody Surrogate antibody clone#75-54.7 (BioXcell, BE0247) and an isotype control antibody anti-Hel-mIgG1) were added to each well to a final antibody concentration of 10 μg / mL and incubated in an incubator for 30 minutes. Then, 50 μL of medium containing mouse IL-2 (brand Gibco, catalog number 51061-MNAE, final concentration 300IU) and mouse TNFα (brand Gibco, catalog number 20180502, final concentration 50ng / mL) and 50 μL of medium without or with Dynabeads mouse T-activator CD3 / CD28 (Gibco, catalog number: 11452D, beads to Treg cell ratio 1:20) were added to each well, making the final volume of each well 200 μL. At the same time, control wells were set up for Treg cells + mouse IL-2 only, Treg cells + mouse TNFα only, and Treg cells + mouse IL-2 and human TNFα. Two parallel wells were set up for each condition, and the plates were mixed and cultured in a 37℃ incubator for 3 days for FACS detection (Thermo Attune NxT). The inhibitory effect of the antibody on TNFα-induced Treg proliferation was determined by the percentage of Treg proliferation. Figure 13A shows that Treg cells from TNFR2 HuGEMM mice express human TNFR2 but not mouse TNFR2, and Treg cells from WT Balb / c mice express only mouse TNFR2. Figures 13B and 13C show that the addition of mIL-2 and mTNFα or hTNFα significantly increased the proliferation of TNFR2 HuGEMM Tregs, regardless of whether Dynabeads mouse T-activator CD3 / CD28 agonist was present in the system, suggesting that TNFR2-mediated signals are preserved after genetic modification of TNFR2 HuGEMM mice.On the other hand, in WT balb / c cells, proliferation was increased only by the addition of mIL-2 and mTNFα, whereas hTNFα had no effect on proliferation, suggesting that hTNFα does not bind to mTNFR2. For TNFR2 HuGEMM Tregs, when anti-TNFR2 humanized antibodies were added in the presence of mIL-2 and mTNFα, 001-Hu3-mIgG1 and 219-Hu1-mIgG1 were able to significantly inhibit the proliferation of TNFR2 HuGEMM Tregs compared to the negative control anti-Hel-mIgG1, with a statistical difference (***p<0.001), while the anti-mouse TNFR2 substituted antibody TR75-54.7 had no inhibitory effect. For WT Balb / c Tregs, when anti-TNFR2 antibodies were added in the presence of mIL-2 and mTNFα, compared to the negative control Hamster IgG, the anti-mouse TNFR2 substituted antibody TR75-54.7 was able to significantly inhibit the proliferation of WT Balb / c Tregs, with a statistical difference (***p<0.001), while 001-Hu3-mIgG1 and 219-Hu1-mIgG1 had no inhibitory effect.

[0055] Example 15: Efficacy evaluation of anti-TNFR2 antibodies in a TNFR2 HuGEMM mouse tumor model In cooperation with Baiaosaitu Gene Biotechnology Co., Ltd., we used the EGE system developed by the company based on CRISPR / Cas9 to replace part of Exon2 and Exon3 of the mTNFR2 gene in mouse CT26 cell line with PuroR cassette for gene knockout, disrupting the expression of mouse endogenous mTNFR2, and then inserted the mouse intracellular domain and transmembrane domain into the CDS of human extracellular domain chimeric protein to generate a CT26 cell line (CT26-hTNFR2 KI) that expresses only the hTNFR2 gene. Using TNFR2 HuGEMM, we established a CT26-hTNFR2 KI cell line colon cancer animal model with hTNFR2 gene knocked in, and performed efficacy experiments of anti-TNFR2 antibodies. One CT26-hTNFR2 KI cell was taken from the cell bank and cultured in complete 1640 medium (1640 (Gibco, 61870-036) + 10% FBS (Gibco, 10099-141C) + 1% P / S (Gibco, 15140-122) + 1% NEAA (Gibco, 11140-050) + 1% Sodium Pyruvate (Gibco, 11360-070) + 16 μg / mL Recover the cells with puromycin (Gibco, A11138-03), place the recovered cells in a cell culture flask (write the cell type, generation, date, name of the culturer, etc. on the wall of the flask), and culture in a CO2 incubator (incubator temperature 37 °C, CO2 concentration 5%). After the cells cover 80% to 90% of the bottom of the culture flask, they are passaged, and the passaged cells continue to be cultured in a CO2 incubator. This process is repeated until the cell number meets the requirements for the in vivo drug efficacy experiment, after which a cell suspension is prepared and counted with a fully automated cell counter (BECKMAN, Vi-Cell XR). According to the counting results, the cells are resuspended in PBS (HyClone, SH30256.01) solution, and the cell suspension (density 2 × 10 6 The cell suspension was inoculated subcutaneously on the right side of the mice at 100 μL per mouse, and the tumor volume was approximately 100 mm 3 When tumor volume reached 1000 mg / kg, mice with medium tumor volume were selected and placed into groups. Using a random grouping method based on random numbers in EXCEL, the animals were assigned to eight experimental groups according to tumor volume, as shown in Table 9. Administration began on the same day (denoted as Day 0), with a dose of 10 mL / kg and PBS as the solvent, administered once every three days by intraperitoneal injection for a total of four times. Tumor volume and body weight were measured three times a week at fixed times. Tumor volume calculation formula: tumor volume (mm 3) = length (mm) × width (mm) × width (mm) / 2, calculation formula for tumor inhibition rate: TGI (%) = [1-T / C] × 100%, both experimental data were analyzed using the statistical method of Two-way ANOVA. On the 11th day after administration, compared with the control group, each dose group of the experimental anti-TNFR2 antibody group had a statistical difference compared with the PBS control group, and the efficacy was obvious, and there was also a dose-dependent relationship between different dose groups of the same antibody, and at the same time, the efficacy of the positive drug anti-mPD-1 (BioXcell, BE0146) at 10mpk was equivalent to the efficacy of the experimental anti-TNFR2 antibodies 219-Hu1-mIgG2a and 001-Hu3-mIgG2a at a dose of 3mpk (mg / kg), and these results showed that the experimental anti-TNFR2 humanized antibody had a significant tumor growth inhibitory effect in vivo, and had a dose-dependent relationship (Figure 14A and Figure 14B, Table 10). At the same time, the experimental animals in each group were active and fed well during the administration period, and both their body weight and body weight change rate increased to a certain extent, indicating that the anti-TNFR2 humanized antibody tested had low safety risks in vivo (Figures 15A-D).

[0056] [Table 9]

[0057] [Table 10]

[0058] Example 16: Efficacy evaluation of anti-TNFR2 antibodies in a human PBMC-immunoreconstituted humanized mouse colon tumor model Select 7- to 9-week-old NOG female mice (purchased from Beijing Weitong Lihua Laboratory Animal Technology Co., Ltd.) and subcutaneously inject 3.5 × 10 6 HT-29 cells were inoculated (day 0 of the experiment) and 7 × 10 6Human peripheral blood mononuclear cells (PBMCs, donor #193 and donor #272, extracted from whole blood of donors screened by Zhongmei Crown Bio-Tech (Taicang) Co., Ltd. according to SOP-CP-042) were injected to establish a PBMC humanized colon cancer model. The tumor volume was 95 mm 3 When the tumor volume reached 100 mg / kg, mice with medium tumor volume were selected and placed into groups, and randomly divided into groups according to tumor volume using Study DirectorTM (version number 3.1.399.19, supplier Studylog System, Inc., San Francisco, CA, USA). The animals were assigned to five experimental groups (G1: PBS control group, G2: control antibody anti-Hel hIgG1 group, G3: anti-TNFR2 antibody 001-Hu3-hIgG1 group, G4: anti-TNFR2 antibody 219-Hu1-hIgG1 group, G5: Keytruda group), and 5 to 7 mice were assigned to each group from two donors and used for the in vivo pharmacodynamics study. Administration began on the same day of grouping (day 13). The dose was 10 mg / kg for each group, administered intraperitoneally twice a week. Tumor volume and body weight were measured twice a week at fixed times. The formula for calculating tumor volume (TV) was V=1 / 2×a×b 2 In donor #193, tumor growth in the 219-Hu1 group was significantly inhibited compared to the control antibody group on day 29 after tumor inoculation, with statistical difference (p<0.0001), and the other groups had no statistical difference compared to the control antibody group. In donor #193, the anti-TNFR2 antibody 219-Hu1 was shown to have significant efficacy (Figure 16A). In donor #272, tumor growth in the 001-Hu3, 219-Hu1, and Keytruda groups was all significantly inhibited compared to the control antibody group on day 29 after tumor inoculation, with statistical difference (p<0.0001). In donor #272, Keytruda and the anti-TNFR2 antibodies 001-Hu3 and 219-Hu1 were all shown to have efficacy (Figure 16B). During the experiment, both the control and treated mice lost weight and died. Veterinarian autopsy results suggested that the mice died due to host immune rejection (GvHD) caused by the injection of PBMC. At the dose of 10 mg / kg of the test drugs 001-Hu3, 219-Hu1, and the positive drug Keytruda, the animals showed no obvious drug toxicity and were able to tolerate the treatment (Figure 16C-D). 48 h after the last dose, mice from the G2 control antibody group, the G3 anti-TNFR2 antibody 001-Hu3 group, and the G4 anti-TNFR2 antibody 219-Hu1 group were selected to isolate tumor-infiltrating immune cells (TILs) (Miltenyi, Cat. No. 130-095-929), FACS immunophenotyping was performed, and 123 count eBeads (eBioscience, Cat. No. 01-1234-42) were added for absolute cell counting, and all cell populations were gated based on the FMO control (Figure 17A). The experimental results showed that, compared with the control antibody group, the proportion of CD4+ T cells in the donor #193 anti-TNFR2 antibody treatment group was reduced, but there was no significant difference in the number, and there was no significant difference in the proportion and number of CD4+ T cells in the donor #272 anti-TNFR2 antibody treatment group (Figures 17B-C, E-F). Compared with the control antibody group, the proportion of CD8+ T cells in the donor #193 anti-TNFR2 antibody treatment group was increased, but there was no significant difference in the number and there was no significant difference in the proportion of CD8+ T cells, but there was no significant difference in the proportion of CD8+ T cells in the 001-Hu3 antibody treatment group. The number of CD8+ T cells increased significantly (Figure 17B-C, E-F), and the results of two donors showed that the proportion and number of Treg (CD4+CD25+Foxp3+ cells) cells in the anti-TNFR2 antibody treatment group were significantly lower than those in the control antibody group, with a significant difference (Figure 17B-C, E-F). At the same time, the ratio of the total number of CD8+ T cells to the number of Treg cells in the anti-TNFR2 antibody treatment group (CD8+T / Treg) was also significantly higher than that in the control antibody group, with a statistical difference (Figure 17D, G). From the above data, it can be seen that administration of anti-TNFR2 antibody can significantly increase the CD8+T / Treg ratio of TILs and suppress tumor growth.

[0059] Example 17: Detection of the combined effect of 219-Hu1-hIgG1 monoclonal antibody and anti-mouse PD-L1 monoclonal antibody in a TNFR2 humanized BALBc mouse model The combined effect of 219-Hu1-hIgG1 antibody and anti-mouse PD-L1 (anti-mPD-L1, BioXcell, BE0101) was evaluated using an animal model in which human TNFR2 gene-modified CT26.1C03 colon cancer cells (hTNFR2 KI-CT26) were subcutaneously inoculated into human TNFR2-expressing genetically modified BALB / c mice (TNFR2 HuGEMM). 5 CT26.1C03 colon cancer cells were inoculated into the mice (day 0 of the experiment). 3 When tumor volume reached 100 mg / kg, mice with medium tumor volume were selected and placed into groups. Using a random grouping method based on random numbers in EXCEL according to tumor volume, the animals were assigned to five experimental groups (G1 was the control group, G2 was the anti-mPD-L1 10 mg / kg antibody group, G3 was the 219-Hu1-hIgG1 10 mg / kg antibody group, G4 was the 219-Hu1-hIgG1 30 mg / kg antibody group, and G5 was the 219-Hu1-hIgG1 10 mg / kg + anti-mPD-L1 10 mg / kg antibody combination group), with 10 animals assigned to each group and used for in vivo pharmacodynamics studies, which began dosing on the same day of grouping (day 10). Administration was by intraperitoneal injection twice a week. Tumor volume and body weight were measured three times a week at fixed times. On the 18th day after tumor inoculation (i.e., the 8th day of administration), the TGI of the G2 anti-mPD-L1 10 mg / kg group, the G3 219-Hu1-hIgG1 10 mg / kg group, and the G4 219-Hu1-hIgG1 30 mg / kg group was compared to the control group (G1). TV The TGI values ​​were 35.1%, 28.2%, and 63.8%, respectively, and the increase in tumor volume was significantly suppressed in these three treatment groups (G2 vs. G1, p value < 0.0001; G3 vs. G1, p value = 0.0002; G4 vs. G1, p value < 0.0001), and the TGI values ​​in the 219-Hu1-hIgG1 10 mg / kg group and the anti-mPD-L1 10 mg / kg group were significantly suppressed (G2 vs. G1, p value < 0.0001; G3 vs. G1, p value = 0.0002; G4 vs. G1, p value < 0.0001). TV The values ​​were similar, but the TGI of the 219-Hu1-hIgG1 30 mg / kg group wasTV The values ​​were significantly higher than those of the 219-Hu1-hIgG1 10mg / kg group and the anti-mPD-L1 10mg / kg group (G2 vs. G4, P value = 0.0002; G3 vs. G4, P value < 0.0001). The above results show that 219-Hu1-hIgG1 showed a dose-dependent effect in the dose range of 10 to 30mg / kg, and the tumor volume decreased with increasing dose. Details are shown in Table 11 and Figure 18. On day 18 after tumor inoculation, the increase in tumor volume was also significantly suppressed in the G5 219-Hu1-hIgG1 10mg / kg + anti-mPD-L1 10mg / kg combination group compared to the control group (G1) (TGI TV value = 66.5, vs. G1, P value < 0.0001), and the mean tumor volume of the G5 219-Hu1-hIgG1 10mg / kg + anti-mPD-L1 10mg / kg combination group was also significantly smaller than the G3 219-Hu1-hIgG1 10mg / kg and G2 anti-mPD-L1 10mg / kg single agent groups (TGI TV G5 vs. G3 vs. G2 = 66.5% vs. 28.2% vs. 35.1%; P value G5 vs. G2 < 0.0001, P value G5 vs. G3 < 0.0001), which indicated that the combination of 219-Hu1-hIgG1 antibody and anti-mPD-L1 antibody could better inhibit tumor growth compared with the two single-agent groups, with a statistical difference (****, p < 0.0001, single-agent group vs. combination group). Specifically, as shown in Table 11 and Figure 18.

[0060] [Table 11]

[0061] Notes: a Mean ± SD. b. Relative tumor growth rate T / C%=T RTV / C RTV ×100%(T RTV : Mean RTV of treatment group, C RTVRelative tumor volume (RTV) was calculated according to the results of tumor measurements, and the formula was RTV = V t / V0, where V0 is the tumor volume measured at the time of administration (i.e., PO-D0), and V t is the tumor volume measured at a given time. c.T.G.I. TV (%) = [1-(Ti-T0) / (Vi-V0)] × 100% (Ti: average tumor volume of the treatment group on day i of administration, T0: average tumor volume of the treatment group on day 0 of administration, Vi: average tumor volume of the solvent control group on day i of administration, V0: average tumor volume of the solvent control group on day 0 of administration). d. Data were analyzed by Two-way ANOVA, vs. G1 Veh, p<0.05 means significant difference, ***: p<0.001, ****: p<0.0001. e. Data were analyzed by Two-way ANOVA, vs. G5 combination group, p<0.05 means significant difference, ****: p<0.0001. f. Data were analyzed by Two-way ANOVA, vs. G4 219-Hu1-hIgG1 30mpk, p<0.05 means significant difference, ***: p<0.001, ****: p<0.0001.

[0062] During the administration period, the experimental animals in each group were in good condition in terms of activity and feeding, and a certain degree of increase in body weight was observed. During the observation period, no deterioration in the mental state, activity state, or body surface observation of the animals in each group was observed, and the animals did not show drug toxicity and had a good safety profile, indicating that the 219-Hu1-hIgG1 antibody and the combination of 219-Hu1-hIgG1 + anti-mPD-L1 antibody are highly safe. Details are shown in Figures 19-20 and Table 12.

[0063] [Table 12]

[0064] On the 18th day after tumor inoculation, the animals in each group were euthanized, and the tumors were isolated and weighed. Compared with the control group (G1), the tumor weight in the G2 anti-mPD-L1 10 mg / kg group was significantly reduced (TGI TW = 37.3%, P value 0.0087), and the tumor weight in the G3 219-Hu1-hIgG1 10 mg / kg group was lower than that in the control group, but there was no statistical difference (TGI TW = 25.9%, P value 0.0830), and the tumor weight in the G4 219-Hu1-hIgG1 30 mg / kg group was also significantly lower than that in the control group (TGI TW = 47.9%, P value 0.0013), and the tumor weight in the G5 219-Hu1-hIgG1 10mg / kg + anti-mPD-L1 10mg / kg combination group was also significantly lower than that in the control group (TGI TW = 43.0%, P value 0.0042), and the tumor weights at the two doses of 219-Hu1-hIgG1 showed a dose-dependent effect, with the tumor weight decreasing with increasing dose, and the tumor weights in the combination group were smaller than those in each single-agent group (G2, G3), but there was no statistical difference (Figure 21, Table 13).

[0065] [Table 13]

Claims

1. 1. A humanized antibody or antigen-binding fragment that specifically binds to TNFR2, the antibody or antigen-binding fragment comprising a heavy chain variable region and a light chain variable region, (1) The heavy chain variable region has a VH sequence selected from SEQ ID NOs: 21, 22, 23, 24, and 25. Including, (2) The light chain variable region has the VL sequence shown in SEQ ID NO:

32. Characterized in that it comprises A humanized antibody or antigen-binding fragment that specifically binds to TNFR2.

2. The antibody comprises a human heavy chain constant region and / or a human light chain constant region. The antibody or antigen-binding fragment of claim 1.

3. The antibody or antigen-binding fragment thereof is conjugated to a therapeutic agent or a tracer. The antibody or antigen-binding fragment of claim 1.

4. The antibody or antigen-binding fragment of claim 1 , wherein the second antigen-binding module specifically binds to an antigen other than TNFR2 or binds to a different TNFR2 epitope than the first antigen-binding module; The other antigens include CD3, CD4, CD5, CD8, CD14, CD15, CD16, CD16A, CD19, CD20, CD21, CD22, CD23, CD25, CD33, CD37, CD38, CD40, CD40L, CD46, CD52, CD54, CD70, CD74, CD80, CD86, CD126, CD138, B7, PD-1, P D-L1, PD-2, CTLA4, PRVIG, TIGHT, HAS, CLDN18.2, MSLN, MUC, Ia, HLA-DR, tenascin, EGFR, VEGF, P1GF, ED-B fibronectin, oncogene products, IL-2, IL-6, IL-15, IL-21, TRAIL-R1, or TRAIL-R2; Multispecific antigen binding molecules.

5. The antibody or antigen-binding fragment of the present invention comprises an extracellular antigen-binding domain, a transmembrane domain, and an intracellular signaling domain, wherein the extracellular antigen-binding domain comprises a TNFR2 humanized antibody or antigen-binding fragment of the present invention according to any one of claims 1 to 3. Chimeric antigen receptors (CARs).

6. 6. An immune effector cell, characterized in that the immune effector cell comprises the chimeric antigen receptor of claim 5 or comprises a nucleic acid fragment encoding the chimeric antigen receptor of claim 5. Immune effector cells.

7. Characterized in that it encodes the antibody or antigen-binding fragment according to any one of claims 1 to 3. An isolated nucleic acid fragment.

8. 10. A method of preparing an immune effector cell in vitro according to claim 7, said method comprising introducing into said immune effector cell a nucleic acid fragment encoding the CAR according to claim 6, and optionally said method further comprising initiating expression of the CAR according to claim 5 by said immune effector cell. method.

9. A pharmaceutical composition, characterized in that the composition comprises an antibody or antigen-binding fragment according to any one of claims 1 to 3, a multispecific antigen-binding molecule according to claim 4, a chimeric antigen receptor according to claim 5, an immune effector cell according to claim 6, or a nucleic acid fragment according to claim 7. Pharmaceutical compositions.

10. A drug for treating and / or preventing a disease associated with immune abnormality, comprising the antibody or antigen-binding fragment according to any one of claims 1 to 3, the multispecific antigen-binding molecule according to claim 4, the chimeric antigen receptor according to claim 5, the immune effector cell according to claim 6, or the nucleic acid fragment according to claim 7, The disease is cancer or an autoimmune disease. Drugs.

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