Anti-human TIGIT monoclonal antibody TIGIT-M011 or functional fragment thereof and application thereof

Abstract

The invention belongs to the technical field of biomedicine and antibody engineering. The invention relates to the field of immunoconjugates, in particular to an anti-human TIGIT monoclonal antibody TIGIT-M011 or a functional fragment thereof and application of the anti-human TIGIT monoclonal antibody TIGIT-M011 or the functional fragment thereof as an immunoconjugate, a chimeric antigen receptor and / or a composition, and particularly discloses a monoclonal antibody capable of binding to human TIGIT protein or an antigen binding fragment thereof. The TIGIT specific monoclonal antibody obtained by screening has high sensitivity, high specificity and high affinity.

Description

Technical Field

[0001] The present invention belongs to the field of biomedicine and antibody engineering technology; more specifically, it relates to anti-human TIGIT antibodies or functional fragments thereof, and the use of anti-human TIGIT antibodies or functional fragments thereof as immunoconjugates, chimeric antigen receptors and / or compositions. Background Art

[0002] Immunotherapy provides a new approach to tumor treatment. Antibody drugs represented by immune checkpoint inhibitors such as programmed cell death receptor 1 (PD-1), programmed cell death ligand 1 (PD-L1), cytotoxic T lymphocyte-associated antigen 4 (CTLA4) and lymphocyte activation gene-3 (LAG-3) have benefited patients with various tumors. However, most patients show initial no response to the drug or partial response, and tumor progression still occurs in patients, which may be related to the presence of other immunosuppressive molecules and incomplete activation of the immune system. Screening and combining new immunotherapy targets and optimizing treatment strategies are a major development trend in current tumor treatment.

[0003] TIGIT (T cell immunoglobulin and ITIM domains) is also known as V-set and transmembrane domain-containing protein 3 (VSTM3), V-set and immunoglobulin domain-containing protein 9 (V-set and immunoglobulin domain-containing protein 9, V SIG9) and WUCAM (Washington University cell adhesion molecule), is one of the new immunosuppressive receptors that have attracted much attention in recent years. TIGIT is composed of an extracellular IgV domain, a type I transmembrane protein region, an immunoreceptor tyrosine-based inhibitory motif (ITIM), and a cytoplasmic tail of an immunoglobulin tail tyrosine-like motif (ITT). It is expressed on the surface of activated T cells, natural killer cells (NK), regulatory T cells (Treg) and CD4 helper T cells (Th). TIGIT has three ligands, namely CD155 (PVR), CD112 (PVRL2, Nectin-2) and CD113 (Nectin-3). Among them, TIGIT has the highest affinity with CD155, which has been identified in dendritic cells (DC), macrophages and many human cancer cells, and has been shown to downregulate T cell activation and cytokine secretion after binding to TIGIT. Inhibition of TIGIT / PVR interaction can mediate effective anti-tumor activity of immune cells. DNAM-1 (CD226) is an activating receptor found on NK cells, monocytes and T cells. TIGIT and DNAM-1 compete for shared ligands CD155 and CD112 expressed by tumor cells and antigen-presenting cells. Binding of TIGIT to CD155 or CD112 leads to immunosuppression, while binding of DNAM-1 to the same ligand mediates immune activation. Therefore, TIGIT is also a potential target for tumor immunotherapy. TIGIT antibody anti-tumor research is currently in the clinical trial stage, and the fastest is in Phase III clinical trials.

[0004] Most of the existing TIGIT monoclonal antibodies are prepared by mouse hybridoma technology. Advances in antibody engineering technology have promoted the preparation of antibodies and improved their detection performance. Phage antibody library technology can be used to screen antibodies specific to any antigen. This study used an immune mouse phage antibody library to screen high-performance monoclonal antibodies against human TIGIT protein, which was able to obtain high-affinity antibodies compared to mouse hybridoma antibody screening technology. Summary of the invention

[0005] In a first aspect, the present invention provides a monoclonal antibody or an antigen-binding fragment thereof that can bind to a human TIGIT protein, wherein the anti-human TIGIT monoclonal antibody comprises a heavy chain variable region (VH) and a light chain variable region (VL) complementary determining region sequence, wherein the heavy chain variable region and the light chain variable region complementary determining region respectively contain CDR1, CDR2 and CDR3;

[0006] The amino acid sequence of the heavy chain variable region CDR region is as follows:

[0007] The amino acid sequence of VHCDR1 is SEQ ID NO.1;

[0008] The VHCDR2 amino acid sequence is selected from one or more of SEQ ID NO.2, SEQ ID NO.3, SEQ ID NO.4 and SEQ ID NO.5;

[0009] The amino acid sequence of VHCDR3 is SEQ ID NO.6 and / or SEQ ID NO.7;

[0010] The amino acid sequence of the light chain variable region CDR region is as follows:

[0011] The VLCDR1 amino acid sequence is selected from one or more of SEQ ID NO.8, SEQ ID NO.9, SEQ ID NO.10 and SEQ ID NO.11;

[0012] The amino acid sequence of VLCDR2 is SEQ ID NO.12 and / or SEQ ID NO.13;

[0013] The VLCDR3 amino acid sequence is selected from one or more of SEQ ID NO.14, SEQ ID NO.15, SEQ ID NO.16 and SEQ ID NO.17.

[0014] Among them, when the VHCDR1 amino acid sequence selects SEQ ID NO.1, the VHCDR2 amino acid sequence selects SEQ ID NO.2, and the VHCDR3 amino acid sequence selects SEQ ID NO.6; the VLCDR1 amino acid sequence selects SEQ ID NO.8, the VLCDR2 amino acid sequence selects SEQ ID NO.12, and the VLCDR3 amino acid sequence selects SEQ ID NO.14, the monoclonal antibody that can bind to the human TIGIT protein is TIGIT-M001, and the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M001 that can bind to the human TIGIT protein are shown in SEQ ID NO.18 and SEQ ID NO.19, respectively; the VH and VL nucleotide sequences of TIGIT-M001 are shown in SEQ ID NO.32 and SEQ ID NO.33, respectively.

[0015] When the amino acid sequence of VHCDR1 is selected as SEQ ID NO.1, the amino acid sequence of VHCDR2 is selected as SEQ ID NO.3, and the amino acid sequence of VHCDR3 is selected as SEQ ID NO.7; the amino acid sequence of VLCDR1 is selected as SEQ ID NO.9, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.13, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.15, the monoclonal antibody that can bind to human TIGIT protein is TIGIT-M003; the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M003 that can bind to human TIGIT protein are shown in SEQ ID NO.20 and SEQ ID NO.21, respectively; the VH and VL nucleotide sequences of TIGIT-M003 are shown in SEQ ID NO.34 and SEQ ID NO.35, respectively.

[0016] When the amino acid sequence of VHCDR1 is selected as SEQ ID NO.1, the amino acid sequence of VHCDR2 is selected as SEQ ID NO.2, and the amino acid sequence of VHCDR3 is selected as SEQ ID NO.6; the amino acid sequence of VLCDR1 is selected as SEQ ID NO.10, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.12, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.16; the monoclonal antibody that can bind to human TIGIT protein is TIGIT-M006; the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M006 that can bind to human TIGIT protein are shown in SEQ ID NO.22 and SEQ ID NO.23, respectively; the VH and VL nucleotide sequences of TIGIT-M006 are shown in SEQ ID NO.36 and SEQ ID NO.37, respectively.

[0017] When the amino acid sequence of VHCDR1 is selected as SEQ ID NO.1, the amino acid sequence of VHCDR2 is selected as SEQ ID NO.4, and the amino acid sequence of VHCDR3 is selected as SEQ ID NO.6; the amino acid sequence of VLCDR1 is selected as SEQ ID NO.11, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.13, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.15, the monoclonal antibody that can bind to human TIGIT protein is TIGIT-M007; the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M007 that can bind to human TIGIT protein are shown in SEQ ID NO.24 and SEQ ID NO.25, respectively; the VH and VL nucleotide sequences of TIGIT-M007 are shown in SEQ ID NO.38 and SEQ ID NO.39, respectively.

[0018] When the amino acid sequence of VHCDR1 is selected as SEQ ID NO.1, the amino acid sequence of VHCDR2 is selected as SEQ ID NO.5, and the amino acid sequence of VHCDR3 is selected as SEQ ID NO.6; the amino acid sequence of VLCDR1 is selected as SEQ ID NO.10, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.13, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.17, the monoclonal antibody that can bind to human TIGIT protein is TIGIT-M011; the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M011 that can bind to human TIGIT protein are shown in SEQ ID NO.26 and SEQ ID NO.27, respectively; the VH and VL nucleotide sequences of TIGIT-M011 are shown in SEQ ID NO.40 and SEQ ID NO.41, respectively.

[0019] When the amino acid sequence of VHCDR1 is selected as SEQ ID NO.1, the amino acid sequence of VHCDR2 is selected as SEQ ID NO.2, and the amino acid sequence of VHCDR3 is selected as SEQ ID NO.6; the amino acid sequence of VLCDR1 is selected as SEQ ID NO.10, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.13, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.17, the monoclonal antibody that can bind to human TIGIT protein is TIGIT-M013; the VH and VL amino acid sequences of the monoclonal antibody TIGIT-M013 that can bind to human TIGIT protein are shown in SEQ ID NO.28 and SEQ ID NO.29, respectively; the VH and VL nucleotide sequences of TIGIT-M013 are shown in SEQ ID NO.42 and SEQ ID NO.43, respectively.

[0020] Furthermore, the sequences of the complementary determining regions of the heavy chain variable region (VH) and light chain variable region (VL) of the monoclonal antibody that can bind to the human TIGIT protein also include mutant sequences thereof, and the mutant sequences have at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, and at least 99% sequence identity.

[0021] Furthermore, the monoclonal antibody or antigen-binding fragment thereof that can bind to human TIGIT protein comprises an antibody constant region Fc, and the constant region comprises a heavy chain constant region and a light chain constant region.

[0022] Furthermore, the light chain constant region of the monoclonal antibody or antigen-binding fragment thereof that can bind to human TIGIT protein includes a κ-type or λ-type light chain constant region.

[0023] Furthermore, the heavy chain constant region of the monoclonal antibody or antigen-binding fragment that can bind to human TIGIT protein is selected from the heavy chain constant region of any one of IgD, IgE, IgM, IgA and IgG.

[0024] Furthermore, the heavy chain constant region IgG includes IgG1, IgG2a, IgG2b, IgG3 and IgG4.

[0025] Furthermore, the antigen-binding fragment includes an antigen-binding functional fragment.

[0026] Furthermore, the functional fragment is selected from one or more of Fab, Fab', F(ab')2, Fv or scFv.

[0027] Furthermore, the heavy chain constant region is preferably IgG1, and the amino acid sequence is shown in SEQ ID NO.30.

[0028] Furthermore, the light chain constant region is preferably of κ type, and its amino acid sequence is shown in SEQ ID NO.31.

[0029] In one embodiment, when the heavy chain constant regions of the monoclonal antibodies or antigen-binding fragments that can bind to human TIGIT protein are the same, the nucleotide sequence of the heavy chain constant region is as shown in SEQ ID NO.44.

[0030] In another embodiment, when the light chain constant regions of the monoclonal antibodies or antigen-binding fragments that can bind to human TIGIT protein are the same, the nucleotide sequence of the light chain constant region is as shown in SEQ ID NO.45.

[0031] In a second aspect, the present invention provides a nucleic acid molecule encoding the monoclonal antibody or antigen-binding fragment that can bind to the human TIGIT protein as described in the first aspect of the present invention.

[0032] In a third aspect, the present invention provides a vector comprising a nucleic acid molecule for editing the monoclonal antibody or antigen-binding fragment capable of binding to human TIGIT protein as described in the first aspect of the present invention.

[0033] In a fourth aspect, the present invention provides a host cell, wherein the host cell contains a nucleic acid molecule encoding the monoclonal antibody or antigen-binding fragment that can bind to the human TIGIT protein as described in the first aspect of the present invention.

[0034] In a fifth aspect, the present invention provides an immunoconjugate comprising the monoclonal antibody or antigen-binding fragment thereof according to the first aspect of the present invention.

[0035] In a sixth aspect, the present invention provides a chimeric antigen receptor, wherein the chimeric antigen receptor comprises the monoclonal antibody or antigen-binding fragment thereof according to the first aspect of the present invention.

[0036] In a seventh aspect, the present invention provides a composition comprising the monoclonal antibody or antigen-binding fragment thereof, nucleic acid molecule, vector or host cell or immunoconjugate of the present invention.

[0037] In an eighth aspect, provided is the use of the monoclonal antibody or antigen-binding fragment thereof, nucleic acid molecule, vector or host cell, immunoconjugate, chimeric antigen receptor or nucleic acid molecule, construct or vector encoding thereof, transformed immune cell and / or the composition described in the fifth aspect of the present invention in the preparation of a drug for positively regulating immune cell activity and / or enhancing immune response.

[0038] Furthermore, the application may include application in the preparation of drugs for preventing and / or treating tumors, infections or infectious diseases.

[0039] In the ninth aspect, the present invention provides a kit for detecting TIGIT protein, the kit comprising instructions and a detection reagent, the detection reagent being the monoclonal antibody or its antigen-binding fragment, nucleic acid molecule, vector or host cell, immunoconjugate, chimeric antigen receptor or its encoding nucleic acid molecule, construct or vector, transformed immune cell and / or the reagent of the composition described in the fifth aspect of the present invention.

[0040] Beneficial Effects

[0041] The TIGIT-specific monoclonal antibody finally screened by the present invention has high sensitivity, high specificity and high affinity, and can bind to CD8 + The TIGIT protein on the surface of T cells can be bound and specifically recognize the TIGIT protein on the surface of the cell membrane; the TIGIT antibody in the present invention has significantly higher affinity than the commercially available TIGIT monoclonal antibody (A15153G). BRIEF DESCRIPTION OF THE DRAWINGS

[0042] Figure 1 The purity of TIGIT antibody was determined by SDS-PAGE. (A: Detection results under non-reducing conditions; B: Detection results under reducing conditions; M: Marker; 1: TIGIT-M001; 2: TIGIT-M003; 3: TIGIT-M006; 4: TIGIT-M007; 5: TIGIT-M011; 6: TIGIT-M013).

[0043] Figure 2 ELISA identification of TIGIT protein specificity for TIGIT antibody detection.

[0044] Figure 3 Western blotting identification of TIGIT protein specificity for TIGIT antibody detection. (M: Marker; 1: TIGIT recombinant protein under non-reducing conditions; 2: TIGIT recombinant protein under reducing conditions.)

[0045] Figure 4 Flow cytometric identification of TIGIT protein expressed on the surface of 293FT cells for TIGIT antibody recognition.

[0046] Figure 5 ELISA characterization of the sensitivity of TIGIT antibody to recognize TIGIT protein.

[0047] Figure 6Identification of the affinity of TIGIT antibody binding to TIGIT protein (the lines from top to bottom indicate TIGIT antibody concentrations of 250 nM, 125 nM, 62.5 nM and 31.3 nM, respectively).

[0048] Figure 7 Flow cytometric identification of TIGIT protein on the surface of T cells recognized by TIGIT antibodies. DETAILED DESCRIPTION

[0049] The specific embodiments of the present invention are further described below. It should be noted that the description of these embodiments is used to help understand the present invention, but does not constitute a limitation of the present invention. In addition, the technical features involved in each embodiment of the present invention described below can be combined with each other as long as they do not conflict with each other.

[0050] The experimental methods in the following examples are conventional methods unless otherwise specified, and the experimental materials used in the following examples are commercially available unless otherwise specified.

[0051] The terms "VH" and "VL" as used herein refer to the variable regions of the heavy and light chains of antibodies. The variable region consists of discrete, well-defined subregions called "complementarity determining regions" (CDRs, also called HVRs (hypervariable regions)) and "framework regions" (FRs). CDRs refer to amino acids within the variable region of an antibody that confer antigen specificity and / or binding affinity, separated by FRs. There are three CDRs (VLCDR1, VLCDR2, and VLCDR3) in each antibody light chain variable region, and three CDRs (VHCDR1, VHCR2, and VHCDR3) in each antibody heavy chain variable region; the "complementarity determining regions" (CDRs) of the VH and VL regions alternate with more conserved regions of the "framework regions" (FRs); each VH and VL consists of three CDRs and four FRs, arranged in the following order from the amino terminus to the carboxyl terminus: FR1, CDR1, FR2, CDR2, FR3, CDR3, and FR4.

[0052] As used herein, the term "expression" refers to the process of producing a polypeptide based on a nucleic acid molecule such as a coding sequence of a gene. The process may include transcription, post-transcriptional control, post-transcriptional modification, translation, post-translational control, post-translational modification, or any combination thereof.

[0053] Example 1 Preparation of mouse anti-human TIGIT monoclonal antibody

[0054] 1.1 Animal immunization

[0055] BALB / c mice aged 6-8 weeks were selected. After one week of feeding without abnormality, they were numbered and blood was collected from the retro-orbital venous plexus, about 0.1 ml. After standing at room temperature for 1 hour, the mice were kept at 4°C overnight. After centrifugation at 1500g, the upper serum was taken and stored at -20°C for inspection. For basic immunization, 100 μg of TIGIT-His recombinant protein (Sino Biological Shenzhou) was emulsified and mixed with an equal volume of Freund's complete adjuvant, and immunized by multiple subcutaneous injections in the abdomen and back. Boost immunization was performed at intervals of 3 weeks. An equal amount of TIGIT recombinant protein was emulsified and mixed with Freund's incomplete adjuvant, and immunized by multiple subcutaneous injections. After three boost immunizations, blood was collected from the retro-orbital vein 7 days later to detect serum titer. The mice rested for one month, and mice with higher titers were selected for intraperitoneal injection of 100 μg of TIGIT recombinant protein for shock immunization. The mice were killed on the third day after immunization, and the spleen was collected and quickly transferred to liquid nitrogen for freezing.

[0056] 1.2 Potency Testing Process

[0057] TIGIT recombinant protein was diluted to 5 μg / ml with coating buffer and added to a 96-well ELISA plate, 100 μl / well, oscillated and mixed, sealed with plastic wrap, and incubated at 4°C overnight; washed three times with a plate washer, patted the ELISA plate dry, added 200 μl / well blocking solution to block nonspecific binding sites, 37°C, 2h; washed three times with a plate washer, added 100 μl / well of graded diluted serum, reacted at 37°C for 2h; washed five times with a plate washer, added 1:5000 diluted horseradish peroxidase-labeled goat anti-mouse IgG (H+L), 100 μl / well, reacted at 37°C for 1h; washed five times with a plate washer, added 100 μl / well of color development solution, and incubated at 37°C for 30min; added 50 μl / well of stop solution; measured OD with an ELISA reader 450 The mouse serum dilution was 1:16000, the antibody test was positive, and OD 450 Mice with higher values ​​were given a shock immunization.

[0058] 1.3 scFv phage antibody library construction and antibody screening

[0059] Total RNA was extracted from the spleen of immunized mice and reverse transcribed into cDNA. The heavy chain and light chain variable region (V) sequences of the antibody were amplified by RT-PCR. The heavy chain and light chain variable region sequences (VH and VL) encoding the antibody were spliced ​​into the nucleic acid sequence encoding scFv by overlapping extension PCR. The light and heavy chain variable regions were connected by linker and then connected to the phage vector by restriction endonuclease digestion. The scFv phage antibody library was obtained by electroporation into X-Blue competent cells. The library capacity was not less than 10 8 .

[0060] The phage library was screened by coating TIGIT recombinant protein with ELISA method, and the "panning-amplification-enrichment" cycle was adopted. Generally, positive clones were obtained after more than 2 rounds. The positive clones detected by ELISA were PCR amplified, enzyme digested and typed, and then sent for sequencing. The appropriate variable region sequence was selected according to the sequencing results.

[0061] 1.4 Antibody expression vector construction

[0062] Using phage solution or plasmid as template, PCR method is used to obtain and amplify light and heavy chain variable region fragments, and the variable region gene fragments are inserted into expression vectors with light and heavy chain signal peptides and light and heavy chain constant regions, respectively, to obtain complete IgG heavy chain (pCMV3-H) and light chain (pCMV3-L) expression vectors. After amplification of plasmids, HEK293 cells are transfected for culture expression, antibody purification, etc.

[0063] Example 2 TIGIT antibody sequence analysis

[0064] Six TIGIT monoclonal antibodies were obtained by screening the scFv phage antibody library, named TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013. The light chain and heavy chain variable region sequences were obtained by sequencing the positive clones. The amino acid sequence analysis of the antibody variable region was analyzed by IGBLAST software (https: / / www.ncbi.nlm.nih.gov / igblast / ), and it was found that the scFv antibody belonged to the VH category and Vκ type; ABodyBuilder software (http: / / opig.stats.ox.ac.uk / webapps / newsabdab / sabpred / abodybuilder / ) further analyzed the three CDR region positions of each antibody VH (heavy chain variable region) and VL (light chain variable region) in Kabat mode.

[0065] The amino acid sequences of the antibody heavy chain variable region CDR (VHCDR) and light chain variable region CDR (VLCDR) are as follows:

[0066] The amino acid sequences of TIGIT-M001-VHCDR1, TIGIT-M001-VHCDR2, and TIGIT-M001-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.2, and SEQ ID NO.6, respectively;

[0067] The amino acid sequences of TIGIT-M001-VLCDR1, TIGIT-M001-VLCDR2 and TIGIT-M001-VLCDR3 are shown in SEQ ID NO.8, SEQ ID NO.12 and SEQ ID NO.14, respectively.

[0068] The amino acid sequences of TIGIT-M003-VHCDR1, TIGIT-M003-VHCDR2, and TIGIT-M003-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.3, and SEQ ID NO.7, respectively;

[0069] The amino acid sequences of TIGIT-M003-VLCDR1, TIGIT-M003-VLCDR2 and TIGIT-M003-VLCDR3 are shown in SEQ ID NO.9, SEQ ID NO.13 and SEQ ID NO.15, respectively.

[0070] The amino acid sequences of TIGIT-M006-VHCDR1, TIGIT-M006-VHCDR2, and TIGIT-M006-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.2, and SEQ ID NO.6, respectively;

[0071] The amino acid sequences of TIGIT-M006-VLCDR1, TIGIT-M006-VLCDR2 and TIGIT-M006-VLCDR3 are shown in SEQ ID NO.10, SEQ ID NO.12 and SEQ ID NO.16, respectively.

[0072] The amino acid sequences of TIGIT-M007-VHCDR1, TIGIT-M007-VHCDR2, and TIGIT-M007-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.4, and SEQ ID NO.6, respectively;

[0073] The amino acid sequences of TIGIT-M007-VLCDR1, TIGIT-M007-VLCDR2 and TIGIT-M007-VLCDR3 are shown in SEQ ID NO.11, SEQ ID NO.13 and SEQ ID NO.15, respectively.

[0074] The amino acid sequences of TIGIT-M011-VHCDR1, TIGIT-M011-VHCDR2, and TIGIT-M011-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.5, and SEQ ID NO.6, respectively;

[0075] The amino acid sequences of TIGIT-M011-VLCDR1, TIGIT-M011-VLCDR2 and TIGIT-M011-VLCDR3 are shown in SEQ ID NO.10, SEQ ID NO.13 and SEQ ID NO.17, respectively.

[0076] The amino acid sequences of TIGIT-M013-VHCDR1, TIGIT-M013-VHCDR2, and TIGIT-M013-VHCDR3 are shown in SEQ ID NO.1, SEQ ID NO.2, and SEQ ID NO.6, respectively;

[0077] The amino acid sequences of TIGIT-M013-VLCDR1-3 are shown in SEQ ID NO.10, SEQ ID NO.13 and SEQ ID NO.17 respectively.

[0078] The amino acid sequences of the antibody heavy and light chain variable regions of TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013 are as follows:

[0079] The VH and VL amino acid sequences of TIGIT-M001 are shown in SEQ ID NO.18 and SEQ ID NO.19, respectively.

[0080] The VH and VL amino acid sequences of TIGIT-M003 are shown in SEQ ID NO.20 and SEQ ID NO.21, respectively.

[0081] The VH and VL amino acid sequences of TIGIT-M006 are shown in SEQ ID NO.22 and SEQ ID NO.23, respectively.

[0082] The VH and VL amino acid sequences of TIGIT-M007 are shown in SEQ ID NO.24 and SEQ ID NO.25, respectively.

[0083] The VH and VL amino acid sequences of TIGIT-M011 are shown in SEQ ID NO.26 and SEQ ID NO.27, respectively.

[0084] The VH and VL amino acid sequences of TIGIT-M013 are shown in SEQ ID NO.28 and SEQ ID NO.29, respectively.

[0085] The amino acid sequences of the heavy chain constant regions of the six antibodies are all the same, and their heavy chain constant region amino acid sequences are shown in SEQ ID NO.30.

[0086] The amino acid sequences of the light chain constant regions of the six antibodies are all the same, and their light chain constant region amino acid sequences are shown in SEQ ID NO.31.

[0087] In addition, the nucleotide sequence encoding the antibody is as follows:

[0088] Nucleotide sequence encoding the antibody heavy chain variable region (the underline is the signal peptide coding sequence):

[0089] The VH and VL nucleotide sequences of TIGIT-M001 are shown in SEQ ID NO.32 and SEQ ID NO.33, respectively.

[0090] The VH and VL nucleotide sequences of TIGIT-M003 are shown in SEQ ID NO.34 and SEQ ID NO.35, respectively.

[0091] The VH and VL nucleotide sequences of TIGIT-M006 are shown in SEQ ID NO.36 and SEQ ID NO.37, respectively.

[0092] The VH and VL nucleotide sequences of TIGIT-M007 are shown in SEQ ID NO.38 and SEQ ID NO.39, respectively.

[0093] The VH and VL nucleotide sequences of TIGIT-M011 are shown in SEQ ID NO.40 and SEQ ID NO.41, respectively.

[0094] The VH and VL nucleotide sequences of TIGIT-M013 are shown in SEQ ID NO.42 and SEQ ID NO.43, respectively.

[0095] The nucleotide sequences encoding the heavy chain constant regions of the six antibodies are identical, and the nucleotide sequence of the heavy chain constant region is shown in SEQ ID NO.44.

[0096] The nucleotide sequences encoding the light chain constant regions of the six antibodies are identical, and the nucleotide sequences of the heavy chain constant regions are shown in SEQ ID NO.45.

[0097] As shown in Table 1 are the VHCDR1-3 and VLCDR1-3 sequences described herein;

[0098] Table 1 Sequences of VHCDR1-3 and VLCDR1-3

[0099]

[0100] Table 2 TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013 antibody sequence list

[0101]

[0102]

[0103]

[0104]

[0105]

[0106]

[0107]

[0108]

[0109]

[0110] Example 3 Antibody expression, purification and identification

[0111] The same antibody light chain and heavy chain expression vectors were transiently transfected into HEK293 cells at the same time. The culture supernatant was taken 6-7 days after transfection and affinity purified by protein A purification column to obtain purified antibodies. The antibody molecular weight was predicted based on the protein molecular weight calculator, and the antibody purity and molecular weight were identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

[0112] SDS-PAGE electrophoresis detection process: Take 5 μg of purified antibody respectively, and perform electrophoresis separation, staining, and photographing using 10% SDS-PAGE gel under non-reducing conditions (protein electrophoresis loading buffer does not add β-mercaptoethanol, and the sample is not boiled) and reducing conditions (protein electrophoresis loading buffer adds β-mercaptoethanol, and the sample is boiled for 5 minutes).

[0113] SDS-PAGE test results (see Figure 1 ): The molecular weight of the six antibody heavy chains is predicted to be about 49kDa, the molecular weight of the light chain is predicted to be about 24kDa, and the molecular weight of the whole IgG antibody is predicted to be about 146kDa. SDS-PAGE electrophoresis showed that the protein molecular weight was close to the predicted molecular weight, and the antibody purity was good, about 95%.

[0114] Example 4 Identification of Antibody Specificity and Sensitivity

[0115] 4.1 Antibody specificity identification

[0116] 4.1.1 ELISA to identify TIGIT antibody specificity

[0117] The specificity of TIGIT antibodies was identified using human TIGIT (Hu-TIGIT-His), cynomolgus monkey TIGIT (Cyn-TIGIT-hFc), mouse TIGIT (Ms-TIGIT-hFc), Hu-PD-1-His, Hu-PD-L1-His, Hu-CTLA4-His, Hu-CD137-His, and Hu-TIM-3-His recombinant proteins.

[0118] ELISA detection process: The coating solution was coated with Hu-TIGIT-His, Cyn-TIGIT-hFc, Ms-TIGIT-hFc, Hu-PD-1-His, Hu-PD-L1-His, Hu-CTLA4-His, Hu-CD137-His and Hu-TIM-3-His recombinant proteins, 1μg / ml, overnight at 4°C. The next day, after washing three times with Wash Buffer working solution using a plate washer, 5% skim milk powder was added to block nonspecific binding sites, 200μl / well, and reacted at 37°C for 2 hours. After washing three times with a plate washer, add TIGIT antibody (TIGIT antibody control A15153G and TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013) diluted with 5% skim milk powder to 1 μg / ml, 100 μl / well, and react at 37°C for 2 hours. After washing five times, add 1:5000 diluted horseradish peroxidase-labeled goat anti-mouse IgG (H+L) and react at 37°C for 1 hour. After washing five times, add TMB substrate solution, 100 μl / well, and react at 37°C for 30 minutes. Add stop solution, 50 μl / well. Measure OD using an enzyme reader 450 The test results were analyzed by Graphpad software.

[0119] in:

[0120] The coating solution (BD OptEIACoating Buffer, 51-2713KC) was 0.1 M sodium carbonate at pH 9.5;

[0121] Wash buffer (BD OptEIA Wash Buffer, 51-9003739) 20× concentrated wash buffer, diluted with deionized or distilled water to 1× working solution;

[0122] Color development solution A (BD OptEIA Substrate Reagent A, 51-2606KZ) is a buffer solution containing hydrogen peroxide;

[0123] Chromogen B (BD OptEIA Substrate Reagent B, 51-2607KZ) contains an organic solvent of 3,3',5,5'tetramethylbenzidine (TMB);

[0124] Stop solution (BD OptEIA Stop Solution, 51-2608KZ): 1M sulfuric acid; 5% milk: 5 grams of milk was added to 100 ml of 1×PBS solution.

[0125] Test results (see Figure 2 ): All six TIGIT antibodies can well recognize human TIGIT and cynomolgus monkey TIGIT recombinant proteins. TIGIT-M001, TIGIT-M003 and TIGIT-M013 antibodies weakly cross-bind with mouse TIGIT protein, and TIGIT-M006, TIGIT-M007 and TIGIT-M011 antibodies do not bind to mouse TIGIT protein. This suggests that TIGIT-M001 / TIGIT-M003 / TIGIT-M013 antibodies recognize and bind different TIGIT epitopes from TIGIT-M006, TIGIT007 and M011 antibodies.

[0126] The six antibodies did not bind to human PD-1, PD-L1, CTLA4, CD137 and TIM-3 recombinant proteins, indicating that TIGIT antibodies have good specificity in recognizing and binding to TIGIT proteins. The commercial control antibody A15153G only binds to human TIGIT protein, but not to cynomolgus monkey and mouse TIGIT proteins, indicating that the TIGIT epitopes recognized and bound by the six antibodies are different from those recognized and bound by A15153G.

[0127] 4.1.2 Identification of the specificity of TIGIT antibodies by Western blotting

[0128] The binding properties of TIGIT antibody to TIGIT recombinant protein under non-reducing and reducing conditions were identified by western blotting.

[0129] Western blotting detection process: Take 1μg of TIGIT-His recombinant protein respectively, and use 10% SDS-PAGE gel for electrophoresis separation under non-reducing conditions (protein electrophoresis loading buffer does not add β-mercaptoethanol, and the sample is not boiled) and reducing conditions (protein electrophoresis loading buffer adds β-mercaptoethanol, and the sample is boiled for 5min), 150V, electrophoresis for about 1h. After the electrophoresis, transfer the mold, and transfer the protein separated by SDS-PAGE gel to nitrocellulose membrane, 300mA, 1h. After the transfer, use 5% skim milk powder to block at room temperature for 2h. 0.5μg / ml antibodies (TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013) were bound overnight at 4℃. Wash the membrane 3 times with PBST solution, 5min / time. The secondary antibody was added with horseradish peroxidase-labeled goat anti-mouse IgG (H+L) at a dilution of 1:5000 and reacted at room temperature for 1 hour. Unbound antibodies were removed by washing with PBST. Chemiluminescent substrate was added and the detection results were recorded by gel imaging.

[0130] Test results (see Figure 3 ): TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013 antibodies mainly recognized TIGIT recombinant protein under non-reducing conditions, suggesting that TIGIT antibodies mainly recognized conformational epitopes of TIGIT protein; weak bands appeared at the reducing condition TIGIT protein under strong exposure conditions.

[0131] 4.1.3 Detection of TIGIT protein on cell membrane surface by flow cytometry

[0132] The TIGIT protein expressed on the cell membrane surface of 293FT cells transfected with TIGIT-GFP recombinant plasmid was identified by flow cytometry.

[0133] Flow cytometry detection process: 48 hours after the TIGIT-GFP recombinant plasmid was transfected into 293FT cells, the cells were digested with trypsin to prepare a single cell suspension. The cells to be tested were washed once with PBS, and 1 μg / ml mouse anti-human TIGIT antibodies (TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013) were added respectively, and reacted at room temperature for 30 minutes. After washing once with PBS, 1:1000 diluted AF647 labeled goat anti-mouse IgG (H+L) antibody was added, and reacted at room temperature in the dark for 30 minutes. After washing twice with PBS, the cells were resuspended in 200 μl PBS solution. Using BD LSRFortessa TMThe detection was performed by flow cytometry, and the results were analyzed by BD FACS Diva software.

[0134] Flow cytometry was used to detect the TIGIT protein on the surface of 293FT cells transfected with TIGIT-GFP recombinant plasmid (see Figure 4 ): All TIGIT antibodies can bind to TIGIT protein expressed on the surface of 293FT cells transfected with TIGIT recombinant plasmid

[0135] 4.2 Identification of antibody sensitivity.

[0136] TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013 antibodies detect TIGIT and GFP double positive cells ( Figure 4 The proportions of TIGIT-positive cells in the upper right quadrant of the glioma were 17.9%, 18.2%, 16.8%, 19.1%, 17.5% and 17.0%, respectively. The proportions of TIGIT-positive cells detected by the six antibodies were basically the same.

[0137] 4.2.1 Indirect ELISA to detect TIGIT antibodies and TIGIT protein sensitivity

[0138] Detection process: Hu-TIGIT-His and Hu-TIGIT-hFc recombinant proteins were coated on 96-well ELISA plates with 10-fold gradient dilution (1000-0.001 ng / ml), 100 μl / well, overnight at 4°C. Primary antibodies were added with 1 μg / ml of TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011, TIGIT-M013 and control antibody (A15153G). The remaining steps were the same as the ELISA detection process.

[0139] ELISA sensitivity test results (see Figure 5 ): Through the indirect ELISA method, the sensitivity of the self-developed TIGIT antibody and the control antibody A15153G in detecting TIGIT-His recombinant protein was 100ng / ml, and the sensitivity of detecting TIGIT-hFc recombinant protein was 10ng / ml. The sensitivity of the six self-developed TIGIT antibodies was similar to that of the commercially available TIGIT antibody A15153G.

[0140] Example 5 TIGIT antibody affinity identification

[0141] The antibody affinity was tested by ForteBio Octet molecular interaction instrument. TIGIT-hFc recombinant protein was used as the detection antigen, FORTEBIO anti-human IgG Fc capture (AHC) biosensor was applied, and TIGIT antibody A15153G was used as the control antibody.

[0142] Affinity detection process: FORTEBIO anti-human IgG Fc capture (AHC) biosensor was pre-wetted in equilibration solution (PBS solution of 0.1% BSA + 0.02% Tween20) for 10 minutes, TIGIT-hFc recombinant protein was diluted to 5μg / mL with equilibration solution, and added to the second column of a light-proof 96-well plate, 200μl / well; TIGIT antibody was diluted from 250nM to 31.3nM, added to the fourth column of a light-proof 96-well plate, 200μl / well, and an antibody 0nM blank control was set, and 200μl of equilibration solution was added. The equilibration solution was added to the first and third columns, 200μl / well. ForteBio Octet molecular interaction instrument detection, the sensor was equilibrated in the first column for 60s to obtain the basic equilibrium curve, and then antigen immobilization was performed in the second column for 100s. Wash for 120 seconds in the third column, bind to the antibody for 80 seconds or 180 seconds in the fourth column to obtain a binding curve, return to the first column to dissociate for 300 seconds to obtain a dissociation curve. ForteBio Octet analysis software fits the curve and obtains the affinity value.

[0143] Affinity test results (see Figure 6 ): Antibody affinity was measured using the ForteBio Octet system, using a buffered saline solution without TIGIT protein as a blank control and a commercially available TIGIT antibody A15153G as a detection control.

[0144] After data analysis, the antibody affinity K D The values ​​are 9.28×10 -12 M(TIGIT-M001), 2.42×10 -11 M(TIGIT-M003),1.26×10 -11 M(TIGIT-M006),3.79×10 -11 M(TIGIT-M007),1.40×10 -11 M(TIGIT-M011),8.37×10 -11 M (TIGIT-M013) and 3.51×10 -9 M(A15153G).

[0145] Curve fitting goodness R 2They are 0.9720 (TIGIT-M001), 0.9783 (TIGIT-M003), 0.9815 (TIGIT-M006), 0.8756 (TIGIT-M007), 0.9368 (TIGIT-M011), 0.8643 (TIGIT-M013) and 0.9442 (A15153G). The affinity of the independently developed TIGIT antibody is significantly higher than that of the commercially available TIGIT antibody A15153G.

[0146] Example 6 Flow cytometry identification of TIGIT antibody recognizing TIGIT protein on T cell surface

[0147] Take 200μl of human peripheral blood, add 2ml of red blood cell lysis buffer, and lyse at room temperature for 10min. Centrifuge at 1500rpm for 5min and discard the supernatant. Wash the precipitate once with PBS, and resuspend the cell precipitate by vortexing. Add 1μg of TIGIT antibody (TIGIT-M001, TIGIT-M003, TIGIT-M006, TIGIT-M007, TIGIT-M011 and TIGIT-M013) respectively and react at room temperature for 30min; set up a blank control tube without antibody. After washing with PBS once, add 1:1000 diluted AF647 labeled goat anti-mouse IgG (H+L) antibody and react at room temperature in the dark for 30min. After washing with PBS twice, add CD45 Percp, CD3 BV605, CD4 FITC, CD8APC-H7 antibodies and react at room temperature for 30min. Wash with PBS twice and resuspend the cells in 200μl PBS solution. Use BD LSRFortessa TM The detection was performed by flow cytometry, and the results were analyzed by BD FACS Diva software.

[0148] Flow cytometry detection of TIGIT protein on the surface of T cells ( Figure 7 ): Analysis and selection of CD45 + CD3 + T cells were further analyzed. The results showed that all TIGIT antibodies could bind to CD8 + T cells and CD8 — T cells (mainly CD4 + TIGIT antibodies can be used to detect TIGIT proteins on the surface of endogenous immune cells.

Claims

1. An anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof, wherein the anti-human TIGIT monoclonal antibody TIGIT-M011 comprises heavy chain variable region (VH) and light chain variable region (VL) complementary determining region sequences, wherein the heavy chain variable region and light chain variable region complementary determining regions contain CDR1, CDR2 and CDR3, respectively; wherein, When the amino acid sequence of VHCDR1 is SEQ ID NO.1, the amino acid sequence of VHCDR2 is SEQ ID NO.5, and the amino acid sequence of VHCDR3 is SEQ ID NO.6; When the amino acid sequence of VLCDR1 is selected as SEQ ID NO.10, the amino acid sequence of VLCDR2 is selected as SEQ ID NO.13, and the amino acid sequence of VLCDR3 is selected as SEQ ID NO.17, the VH and VL amino acid sequences of the anti-human TIGIT monoclonal antibody TIGIT-M011 are shown in SEQ ID NO.26 and SEQ ID NO.27, respectively; the VH and VL nucleotide sequences of TIGIT-M011 are shown in SEQ ID NO.40 and SEQ ID NO.41, respectively.

2. The anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof according to claim 1, characterized in that: The antibody or antigen-binding fragment comprises an antibody constant region Fc, wherein the constant region comprises a heavy chain constant region and a light chain constant region; the heavy chain constant region is selected from any one of IgD, IgE, IgM, IgA, IgG1, IgG2a, IgG2b, IgG3 and IgG4; and the light chain constant region is a κ-type or λ-type light chain constant region.

3. The anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof according to claim 1, characterized in that: The antigen-binding fragment includes an antigen-binding functional fragment, and the functional fragment is selected from one or more of Fab, Fab', F(ab')2, Fv or scFv.

4. A nucleic acid molecule encoding the anti-human TIGIT monoclonal antibody TIGIT-M011 or its antigen-binding fragment as claimed in claim 1. 5 . A vector or a host cell, comprising a nucleic acid molecule encoding the anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof according to claim 1 .

6. An immunoconjugate comprising the anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof as claimed in claim 1.

7. A chimeric antigen receptor, comprising the anti-human TIGIT monoclonal antibody TIGIT-M011 or an antigen-binding fragment thereof according to claim 1.

8. A composition comprising the anti-human TIGIT monoclonal antibody TIGIT-M011 or its antigen-binding fragment, nucleic acid molecule, vector or host cell or immunoconjugate as claimed in claim 1.

9. Use of the anti-human TIGIT monoclonal antibody TIGIT-M011 or its antigen-binding fragment, nucleic acid molecule, vector or host cell, immunoconjugate, chimeric antigen receptor or its encoding nucleic acid molecule, construct or vector, transformed immune cell and / or composition as described in claims 1-8 in the preparation of a drug for positively regulating immune cell activity and / or enhancing immune response.

10. A kit for detecting TIGIT protein, the kit comprising instructions and detection reagents, the detection reagents comprising the anti-human TIGIT monoclonal antibody TIGIT-M011 or its antigen-binding fragment, nucleic acid molecule, vector or host cell, immunoconjugate, chimeric antigen receptor or its encoding nucleic acid molecule, construct or vector, transformed immune cell and / or composition reagent involved in the present invention.

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