[go: up one dir, main page]

WO2018098715A1 - Polypeptide et son application - Google Patents

Polypeptide et son application Download PDF

Info

Publication number
WO2018098715A1
WO2018098715A1 PCT/CN2016/108102 CN2016108102W WO2018098715A1 WO 2018098715 A1 WO2018098715 A1 WO 2018098715A1 CN 2016108102 W CN2016108102 W CN 2016108102W WO 2018098715 A1 WO2018098715 A1 WO 2018098715A1
Authority
WO
WIPO (PCT)
Prior art keywords
polypeptide
cancer
tumor
seq
cell
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/CN2016/108102
Other languages
English (en)
Chinese (zh)
Inventor
唐云霞
李波
侯勇
罗顺涛
黄英
刘耿
李冬丽
林秀妹
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BGI Shenzhen Co Ltd
Original Assignee
BGI Shenzhen Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BGI Shenzhen Co Ltd filed Critical BGI Shenzhen Co Ltd
Priority to PCT/CN2016/108102 priority Critical patent/WO2018098715A1/fr
Priority to CN201680090579.2A priority patent/CN110167956B/zh
Publication of WO2018098715A1 publication Critical patent/WO2018098715A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/08—Peptides having 5 to 11 amino acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/10—Cellular immunotherapy characterised by the cell type used
    • A61K40/11—T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/10—Cellular immunotherapy characterised by the cell type used
    • A61K40/19—Dendritic cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/20—Cellular immunotherapy characterised by the effect or the function of the cells
    • A61K40/24—Antigen-presenting cells [APC]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
    • A61K40/41—Vertebrate antigens
    • A61K40/42—Cancer antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/32—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against translation products of oncogenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2239/00—Indexing codes associated with cellular immunotherapy of group A61K40/00
    • A61K2239/31—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterized by the route of administration

Definitions

  • the present invention relates to the field of biomedicine, in particular, the present invention relates to polypeptides and uses thereof, and more particularly to polypeptides and their use in the preparation of kits, medicaments, vaccines, and polypeptides for preventing or treating a subject
  • the use of a disease associated with a mutation in the CCNA2 gene relates to a nucleic acid, a nucleic acid construct, an expression vector, a host cell, a pharmaceutical composition, an antigen presenting cell, an immune effector cell, a vaccine, an antibody, and to a therapeutic method, a diagnostic method, and a diagnostic system.
  • Targeted therapies mainly include monoclonal antibodies (sometimes classified as passive immunotherapy) and small molecule targeted drugs, while immunotherapy mainly includes cytokine therapy, immune checkpoint inhibitors, adoptive cell reinfusion and tumor vaccines.
  • immunotherapy mainly includes cytokine therapy, immune checkpoint inhibitors, adoptive cell reinfusion and tumor vaccines.
  • the immune system enhances the tumor microenvironment's anti-tumor immunity, thereby controlling and killing tumor cells. Therefore, it has the advantages of high efficiency, high specificity, and good tolerance, and has broad prospects in cancer treatment.
  • Tumor immunotherapy vaccines mainly include tumor cell vaccines, dendritic cell (DC cell) vaccines, protein & peptide vaccines, nucleic acid vaccines and genetic engineering vaccines.
  • the main mechanism by which these vaccines can kill tumors is by causing patients to target tumor-specific antigen immune responses, including antigen-antibody reactions and cytotoxic T lymphocyte (CTL)-specific killing, among which CTL-specific killing is in tumor immune response. It has played a big role.
  • a tumor-specific polypeptide is a tumor-specific antigen that primarily causes CTL-specific killing, and includes tumor-mutated polypeptides as well as tumor-specific highly expressed polypeptides.
  • the polypeptide with tumor mutation is a specific target of tumor immunotherapy because it is only present in the tumor tissue of patients, and has the characteristics of good safety and small side effects.
  • Immunotherapy targeting tumor mutant polypeptides is represented by peptide-specific DC-CTL and tumor infiltrating lymphocytes (TIL) adoptive reinfusion, and has good therapeutic effects.
  • Tumor-specific polypeptides are recognized by CTL or TIL cells and require the antigen presentation function of the human leukocyte antigen HLA.
  • Human leukocyte antigens are mainly divided into two subtypes I and II.
  • Type I HLA is mainly divided into three subtypes A, B and C, each of which is subtype. According to their different sequences, the three subtypes A, B and C can be divided into multiple subtypes.
  • HLA-A0201 is one of the HLA-A subtypes, accounting for 13% of the Chinese population. High proportion. The binding of different polypeptides to the HLA-A0201 subtype is different. In tumor patients with specific HLA subtypes, the HLA subtype determines that only a portion of the mutant polypeptide can bind to its HLA and is presented to CTL or TIL cells by its HLA.
  • the inventors found that mutations in the CCNA2 gene resulted in the mutation of the amino acid at position 219 encoded by valerine (Val, V) to phenylalanine (Phe, F).
  • the mutated CCNA2 gene can be specifically expressed at a high level in tumor tissues, and the mutant polypeptide encodes a mutant polypeptide having tumor tissue specificity.
  • the inventors have experimentally verified that the mutant polypeptide sequence has high affinity with HLA-A0201.
  • the present invention proposes an isolated polypeptide.
  • the polypeptide is selected from the group consisting of: (1) a polypeptide having the amino acid sequence set forth in SEQ ID NO: 1; or (2) having at least 70%, at least 75%, at least 80 compared to (1) a polypeptide having %, at least 85%, at least 90%, at least 95%, at least 99% identity; or (3) a polypeptide having one or more amino acid substitutions, deletions, and/or additions compared to (1).
  • the substitution, deletion and/or addition of the at least one or more amino acids is a substitution of amino acid position 2 and/or amino acid 9 of the amino acid sequence set forth in SEQ ID NO: 1.
  • the substitution, deletion and/or addition of the at least one or more amino acids is such that the amino acid sequence of amino acid sequence shown in SEQ ID NO: 1 is substituted with M, and/or the amino acid at position 9 is substituted with L.
  • the polypeptide has the amino acid sequence set forth in SEQ ID NO:2, SEQ ID NO:3 or SEQ ID NO:4. Wherein (2) the polypeptide or (3) the polypeptide has the same function as the polypeptide of (1).
  • the polypeptide has a high affinity for HLA-A0201 and has the ability to activate specific T cell immunity.
  • the invention provides the use of an agent for detecting a polypeptide as described in the preparation of a kit for diagnosing a tumor, optionally wherein the tumor simultaneously expresses HLA-A0201 and the polypeptide
  • the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, preferably The tumor is breast cancer.
  • the above polypeptide is specifically expressed in tumor tissues, and the inventors have further verified by experiments that a kit prepared by using the reagent for detecting the above polypeptide can be effectively used for diagnosing a tumor;
  • the inventors have surprisingly found that the above polypeptide has high affinity with HLA-A0201, and can be presented to CTL or TIL cells by the presenting cells expressing HLA-A0201 to activate specific T cell immunity, when the tumor simultaneously expresses HLA-A0201
  • the safety and effectiveness of the kit is significantly improved; at the same time, the inventors found that breast cancer, lung cancer, nasopharyngeal cancer, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin Cancer, prostate cancer, cervical cancer, leukemia or brain tumor tissue specific
  • the above polypeptide is highly expressed, and when the tumor is the above tumor, especially breast cancer, the validity and sensitivity of the kit diagnosis can
  • the invention provides the use of the above polypeptide for the preparation of a medicament for the prophylaxis or treatment of a tumor, optionally, wherein the tumor simultaneously expresses HLA-A0201 and the polypeptide, optionally
  • the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, preferably,
  • the tumor is breast cancer.
  • the inventors have found that the above polypeptide is specifically highly expressed in tumor tissues, and the inventors have further verified by experiments that the drug prepared by the above polypeptide can be effectively used for preventing or treating a tumor;
  • the safety and efficacy of treatment or prevention are significantly improved;
  • the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanin
  • the effectiveness and sensitivity of treatment or prevention can be further improved in tumors, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumors, especially breast cancer.
  • the invention provides an isolated nucleic acid.
  • the nucleic acid is a nucleic acid encoding the above polypeptide or a complement thereof.
  • the nucleic acid is capable of specifically encoding the above polypeptide.
  • the polypeptide has a high affinity with HLA-A0201 and has the ability to activate specific T cell immunity.
  • the nucleic acid proposed in the examples of the present invention is in a suitable condition.
  • the polypeptide expressed below can be used for the prevention or treatment of tumors, especially when the tumor simultaneously expresses HLA-A0201 and the above polypeptide, and the treatment or prevention is safer and more effective.
  • the invention proposes a nucleic acid construct.
  • the nucleic acid construct comprises a coding sequence which is a nucleic acid as described above, and an optional control sequence operably linked to the coding sequence.
  • the control sequence is one or more control sequences that direct expression of the polypeptide in a host.
  • the nucleic acid construct of the present invention can efficiently express the above polypeptide in a suitable host cell after being ligated to an expression vector under suitable conditions, and can be effectively used for tumors, especially simultaneously expressing HLA-A0201 and the above. Specific treatment or prevention of a tumor of a polypeptide.
  • the invention proposes an expression vector.
  • the vector comprises the nucleic acid construct described above.
  • the expression vector of the embodiments of the present invention can efficiently express the above polypeptide in an expression host under suitable conditions, and the expression vector can be effectively used for specificity of tumors, particularly tumors simultaneously expressing HLA-A0201 and the above polypeptides. Treatment or prevention.
  • the invention proposes a host cell.
  • the cell carries the nucleic acid construct or expression vector described above, optionally obtained by transfection or transformation of the nucleic acid construct or expression vector.
  • the host cell can efficiently express the above polypeptide under suitable conditions, and the host cell can be effectively used for specific treatment or prevention of tumors, particularly tumors simultaneously expressing HLA-A0201 and the above polypeptides. .
  • the invention proposes a pharmaceutical composition.
  • the pharmaceutical composition comprises: a polypeptide as described above; and a pharmaceutically acceptable adjuvant.
  • the inventors have found through extensive experiments that a pharmaceutical composition comprising the aforementioned polypeptide and a pharmaceutically acceptable adjuvant can significantly stimulate the proliferation and secretion of CTL or TIL, and can significantly kill tumor cells presenting the above polypeptide antigen, with significant treatment or Prevention of tumors, especially the efficacy of tumors that specifically express the above polypeptide antigens.
  • the invention provides the use of a polypeptide as described above for the preparation of a vaccine for the prevention or treatment of a tumor, optionally, wherein the tumor simultaneously expresses HLA-A0201 and the polypeptide
  • the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, preferably The tumor is breast cancer.
  • the inventors have found that the above polypeptide is specifically expressed in tumor tissues, and the inventors have further verified by experiments that the vaccine prepared by the above polypeptide can be effectively used.
  • the invention provides an antigen presenting cell.
  • the antigen presenting cell can present a polypeptide as described above.
  • the antigen presenting cell which presents the polypeptide described above is effective to cause an immune response of the patient to the tumor-specific antigen-the above polypeptide, thereby activating the CTL-specific killing function, and the antigen presenting cell proposed by the embodiment of the present invention It has remarkable efficacy in treating tumors expressing HLA-A0201 and the above polypeptides, and the therapeutic effect thereof is remarkable and the safety is high.
  • the invention provides an immune effector cell.
  • the immune effector cell can recognize the aforementioned polypeptide or recognize an antigen presenting cell that presents the aforementioned polypeptide on the surface of the cell.
  • the immune effector cells specifically kill tumor cells that co-express HLA-A0201 and the above polypeptide.
  • the invention proposes a vaccine.
  • the vaccine comprises a nucleic acid as described above, or a nucleic acid construct as described above, or an expression vector as described above, or a host cell as described above, or an antigen presenting cell as described above , or the immune effector cells described above.
  • the nucleic acid or nucleic acid construct or expression vector of the present invention expresses the aforementioned polypeptide under suitable conditions, and the nucleic acid or nucleic acid construct or expression vector of the present invention can be used for the treatment or prevention of expression.
  • the tumor of the polypeptide, the antigen presenting cells proposed in the embodiments of the present invention have significant efficacy in treating tumors expressing HLA-A0201 and the polypeptide, and the immune effector cells proposed in the embodiments of the present invention have significant specific killer presentation Antigen - the role of the target cell of the polypeptide.
  • the vaccine proposed in the examples of the present invention has a remarkable effect of treating or preventing a tumor expressing HLA-A0201 and the polypeptide, which is safer and has fewer side effects.
  • the invention provides an antibody.
  • the antibody specifically recognizes a polypeptide as described above.
  • the antibody proposed in the embodiments of the present invention can specifically bind to the polypeptide, and can specifically recognize tumor cells which specifically express the polypeptide, and the antibody proposed in the embodiment of the invention plays a huge role in tumor diagnosis, treatment or prevention. effect.
  • the invention provides a method of treatment.
  • the method of treatment comprises: administering to the patient a therapeutically effective amount of a polypeptide as described above, a nucleic acid as described above, a nucleic acid construct as described above, an expression vector as described above, as described above Host cell, a pharmaceutical composition as described above, an antigen presenting cell as described above, an immune effector cell as described above, a vaccine as described above or an antibody as described above.
  • the therapeutic method proposed in the examples of the present invention comprises administering any effective amount of the aforementioned polypeptide or the like to effectively treat or prevent a tumor expressing HLA-A0201 and the polypeptide.
  • the invention provides the use of a polypeptide as described above for the prevention or treatment of a disease associated with a mutation in the CCNA2 gene in a subject.
  • the polypeptide of the embodiment of the present invention is useful for preventing or treating a disease associated with a mutation in the CCNA2 gene in a subject.
  • the invention proposes a diagnostic method.
  • the diagnostic method comprises: detecting whether a biological sample derived from a patient carries a polypeptide as described above; determining whether the patient has a tumor based on whether the biological sample carries the polypeptide, optionally The tumor simultaneously expresses HLA-A0201 and the polypeptide, and optionally, the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer , prostate cancer, cervical cancer, leukemia or brain tumor, preferably, the tumor is breast cancer.
  • the inventors have found that the polypeptide is specifically highly expressed in tumor tissues, whereas the polypeptide is absent from normal tissues.
  • the diagnostic method proposed in the embodiments of the present invention can effectively diagnose a tumor which specifically expresses the polypeptide highly patient.
  • the inventors found that breast cancer, lung cancer, nasopharyngeal cancer, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor specific high expression
  • the polypeptide, and further, the method according to the embodiment of the present invention further improves the diagnostic accuracy of the above tumor.
  • HLA-A0201 has a high proportion in the Chinese population, and HLA-A0201 has a strong affinity with the polypeptide, and the polypeptide stimulates a series of immune responses by binding to the cell surface HLA-A0201. . Therefore, the diagnostic method proposed in the examples of the present invention diagnoses a tumor patient who simultaneously expresses HLA-A0201 and the polypeptide with a higher probability.
  • the invention provides a diagnostic system.
  • the diagnostic system includes: a polypeptide detecting device, configured to detect whether a biological sample derived from a patient carries the polypeptide described above; a diagnostic result determining device, the diagnostic result determining device and The polypeptide detecting device is operative to determine whether the patient has a tumor based on whether the biological sample carries the polypeptide, optionally, the tumor simultaneously expresses HLA-A0201 and the polypeptide, optionally,
  • the tumor is breast cancer, lung cancer, nasopharyngeal cancer, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, preferably, the tumor For breast cancer.
  • the inventors have found that the polypeptide is specifically highly expressed in tumor tissues, whereas the polypeptide is absent from normal tissues.
  • the diagnostic system proposed by the embodiments of the present invention can be used to effectively determine a tumor patient that specifically expresses the polypeptide.
  • the inventors found that breast cancer, lung cancer, nasopharyngeal cancer, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor specific high expression
  • the polypeptide, the diagnostic system proposed by the embodiment of the present invention further improves the diagnostic accuracy of the above tumor.
  • HLA-A0201 has a high proportion in the Chinese population, and HLA-A0201 has a strong affinity with the polypeptide, and the polypeptide stimulates a series of immune responses by binding to the cell surface HLA-A0201. .
  • the diagnostic system proposed by the embodiments of the present invention diagnoses a tumor patient who simultaneously expresses HLA-A0201 and the polypeptide with a higher probability.
  • FIG. 1 is a schematic structural view of a diagnostic system according to an embodiment of the present invention.
  • FIG. 2 is a graph showing the results of flow cytometry detection of affinity of T2 cells loaded with polypeptide and HLA-A0201 according to an embodiment of the present invention
  • FIG. 3 is a graph showing the results of an ELISPOTs method for verifying a polypeptide-activated CD8 + T cell immune response according to an embodiment of the present invention
  • FIG. 4 is a graph showing the results of specific killing of activated polypeptide-loaded target cells by activated CD8 + T cells, wherein T cell refers to T cells and T2 refers to T2 cells;
  • Figure 5 is a graph showing the results of immunotherapy of a polypeptide according to an embodiment of the present invention.
  • A shows an adjuvant, adjuvant + wild type ILVDWLVEV (SEQ ID NO: 5) polypeptide group, ILVDWLFEV (SEQ ID NO: 1) polypeptide or a variable form polypeptide thereof (SEQ ID NO: 2 to 4)
  • the sequence shows the effect of each group + adjuvant on inhibiting tumor growth after treatment
  • FIG. B shows the sequence of the adjuvant, adjuvant + wild type ILVDWLVEV (SEQ ID NO: 5) polypeptide, ILVDWLFEV (SEQ ID NO: 1) polypeptide or variant form thereof (SEQ ID NO: 2 to 4) Shows the results of the survival rate of mice after each group + adjuvant treatment;
  • Figure 6 shows a graph of the results of immunotherapy of a polypeptide according to an embodiment of the present invention
  • A shows a DC-loaded wild type (ILVDWLVEV (SEQ ID NO: 5)) polypeptide, a DC-loaded ILVDWLFEV (SEQ ID NO: 1) mutant polypeptide or a variant thereof (SEQ ID NO: 2 to 4) a sequence of peptides that inhibit tumor growth after treatment,
  • Figure 7 shows the results of the immunotherapy of peptides
  • A shows a nucleic acid sequence carrying a wild type ILVDWLVEV (SEQ ID NO: 5) or a mutant polypeptide ILVDWLFEV (SEQ ID NO: 1), or a nucleic acid sequence encoding a mutant polypeptide variable form polypeptide SEQ ID NO: 2 to 4.
  • the lentiviral vector is used for immunotherapy after transfecting DC, inhibiting tumor growth effect map,
  • B shows the slow carrying of the nucleic acid sequence encoding the wild type ILVDWLVEV (SEQ ID NO: 5) or the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1), or the nucleic acid sequence encoding the mutant polypeptide variable form polypeptides SEQ ID NO: 2 to 4.
  • Figure 8 shows the results of the immunotherapy of peptides
  • A shows DC-loaded wild-type (ILVDWLVEV (SEQ ID NO: 5)) polypeptide + CTL, DC-loaded mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) or a variant thereof (SEQ ID NO: 2 - 4)
  • ILVDWLVEV SEQ ID NO: 5
  • A shows performing DC-loaded wild-type (ILVDWLVEV (SEQ ID NO: 5)) polypeptide + CTL, DC-loaded mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) or a variant thereof (SEQ ID NO: 2 - 4)
  • the sequence shows the results of the survival rate of mice after +CTL treatment.
  • first and second are used for descriptive purposes only, and are not to be construed as indicating or implying a relative importance or implicitly indicating the number of technical features indicated. Thus, features defining “first” and “second” may include one or more of the features either explicitly or implicitly. Further, in the description of the present invention, the meaning of "a plurality" is two or more unless otherwise specified.
  • the invention proposes an isolated polypeptide.
  • the polypeptide is selected from the group consisting of: (1) a polypeptide having the amino acid sequence set forth in SEQ ID NO: 1; or (2) having at least 70%, at least 75%, at least 80% compared to (1) a polypeptide having at least 85%, at least 90%, at least 95%, at least 99% identity; or (3) a polypeptide having one or more amino acid substitutions, deletions, and/or additions compared to (1).
  • the polypeptide proposed in the examples of the present invention is derived from a tumor mutant polypeptide, is absent in a human in which the mutation does not occur, and is only present in the tumor tissue of the patient who has the mutation, and the normal tissue does not contain the mutation. Since it is only found in the patient's tumor tissue, and there is no normal tissue, its specificity is higher, and the specificity of the immune response caused is also higher.
  • the CTL produced by the polypeptide stimulated by the polypeptide of the embodiment of the present invention only has a killing effect on tumor cells and tissues, and does not affect the normal group. Weaving to achieve precise targeted therapy for tumors.
  • the use of the polypeptide proposed in the examples of the present invention for tumor immunotherapy not only has a good therapeutic effect, but also has the characteristics of good safety and small side effects.
  • the substitution, deletion and/or addition of the at least one or more amino acids described above is a substitution of amino acid position 2 and/or amino acid 9 of the amino acid sequence set forth in SEQ ID NO: 1.
  • substitution of amino acid sequence 2 and/or amino acid 9 of the amino acid sequence of SEQ ID NO: 1 does not alter the specificity between the amino acid sequence and T cells, and does not alter the immunogenicity of the polypeptide.
  • the substitution, deletion and/or addition of the at least one or more amino acids is such that the amino acid sequence of the amino acid sequence shown in SEQ ID NO: 1 is substituted with M, and/or The 9-position amino acid is substituted for L.
  • the above polypeptide has the amino acid sequence shown as SEQ ID NO: 2, SEQ ID NO: 3 or SEQ ID NO: 4.
  • ILVDWLFEV (SEQ ID NO: 1), IMVDWLFEL (SEQ ID NO: 2), ILVDWLFEL (SEQ ID NO: 3), and IMVDWLFEV (SEQ ID NO: 4) are both high in HLA-A0201. Affinity, both have the ability to activate specific T cell immunity.
  • variable forms of the polypeptide IMVDWLFEL (SEQ ID NO: 2), ILVDWLFEL (SEQ ID NO: 3), IMVDWLFEV (SEQ ID NO: 4) alter the second position of the polypeptide ILVDWLFEV (SEQ ID NO: 1). And/or the 9th position, wherein the amino acid substitution at position 2 is M, and/or the amino acid substitution at position 9 is L.
  • This substitution enhances the binding of the polypeptide to HLA-A0201 without changing it with T cells.
  • the specificity between them does not alter the immunogenicity of the polypeptide.
  • both the SEQ ID NO: 2 to 4 polypeptide and the SEQ ID NO: 1 polypeptide have the ability to activate specific T cell immunity.
  • the present invention provides, in one aspect, the use of an agent for detecting the above polypeptide in the preparation of a kit, the use of the above polypeptide in the preparation of a medicament, and the use of the above polypeptide in the preparation of a vaccine for use in a kit, a medicament or a vaccine. Diagnose, prevent or treat tumors.
  • the tumor simultaneously expresses HLA-A0201 and the polypeptide.
  • the tumor is breast cancer, lung cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, melanoma, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, preferably The tumor is breast cancer.
  • the above polypeptide is specifically expressed in tumor tissues, and the inventors have further verified by experiments that the kit for preparing the above polypeptide or the above polypeptide preparation medicine or vaccine can be effectively used. In the diagnosis of tumors, it is safer and has fewer side effects. At the same time, the inventors have surprisingly found that the above polypeptides have high affinity with HLA-A0201 and can be presented to CTL or TIL cells by presenting cells expressing HLA-A0201.
  • the safety and effectiveness of the kit, drug or vaccine diagnosis or treatment is significantly improved; at the same time, the inventors found that lung cancer, melanoma, Breast cancer, nasopharyngeal carcinoma, liver cancer, gastric cancer, esophageal cancer, colorectal cancer, pancreatic cancer, skin cancer, prostate cancer, cervical cancer, leukemia or brain tumor, especially breast cancer tissue-specific high expression of the above polypeptide, and then as a tumor In the case of the above tumor, the effectiveness of the kit, drug or vaccine diagnosis and treatment can be further improved.
  • the invention provides the use of a polypeptide as described above for preventing or treating a disease associated with a mutation in the CCNA2 gene in a subject.
  • mutations in the CCNA2 gene resulted in the mutation of the amino acid at position 219 encoded by valerine (Val, V) to phenylalanine (Phe, F). .
  • the polypeptide of the embodiment of the present invention has the same antigenic property as the polypeptide encoded by the CCNA2 mutant gene, and the specific immune response caused by the polypeptide has significant effect on the specific recognition and killing effect of the CCNA2 gene mutant cells, and further
  • the polypeptide of the embodiment of the invention may be used for the prevention or treatment of a disease associated with mutation of the CCNA2 gene.
  • the inventors have found through experiments that the polypeptide is effective for preventing or treating a disease associated with a mutation in the CCNA2 gene.
  • the invention provides an isolated nucleic acid.
  • the nucleic acid is a nucleic acid encoding the above polypeptide or a complement thereof.
  • the nucleic acid is capable of specifically encoding the above polypeptide, and as described above, the polypeptide has high affinity with HLA-A0201, The ability to activate specific T cell immunity, and further, the polypeptide expressed by the nucleic acid of the present invention can be used for preventing or treating tumors, especially when the tumor simultaneously expresses HLA-A0201 and the above polypeptide, and the treatment thereof Or prevention is more secure and effective.
  • the invention provides a nucleic acid construct.
  • the nucleic acid construct comprises a coding sequence which is a nucleic acid as described above, and an optional control sequence operably linked to the coding sequence.
  • the control sequence is one or more control sequences that direct expression of the polypeptide in a host.
  • the control sequences include, but are not limited to, U6, H1, CMV, EF-1, LTR or RSV promoters.
  • the nucleic acid construct of the present invention can efficiently express the above polypeptide in a suitable host cell after being ligated to an expression vector under suitable conditions, and can be effectively used for tumors, especially simultaneously expressing HLA-A0201 and the above. Specific treatment or prevention of a tumor of a polypeptide.
  • the invention provides an expression vector.
  • the vector comprises the nucleic acid construct described above.
  • the type of the expression vector is not particularly limited as long as the nucleic acid construct described above can be efficiently expressed in a recipient cell, and the expression vector includes, but is not limited to, a retrovirus vector, a lentiviral vector, and/or a gland. Virus-associated viral vector.
  • the expression vector proposed in the embodiments of the present invention can efficiently express the above polypeptide in an expression host under suitable conditions, and the expression vector can be effectively used for tumors, particularly tumors simultaneously expressing HLA-A0201 and the above polypeptides. Sexual treatment or prevention.
  • the invention provides a host cell.
  • the cell carries the nucleic acid construct or expression vector described above, optionally obtained by transfection or transformation of the nucleic acid construct or expression vector. Transformation or transfection can be carried out by means of electroporation, viral transfection or transformation of competent cells. The manner in which transfection or transformation is employed is determined by the nature of the host cell and the nature of the nucleic acid construct or expression vector to be transduced, as long as the high expression of the aforementioned polypeptide can be achieved in the host cell and the host cell A good cell state does not have a large effect.
  • the host cell can efficiently express the above polypeptide under suitable conditions, and the host cell can be effectively used for specific treatment or prevention of tumors, particularly tumors simultaneously expressing HLA-A0201 and the above polypeptides. .
  • suitable conditions refer to conditions suitable for expression of the polypeptide described herein. It will be readily understood by those skilled in the art that conditions suitable for expression of the polypeptide include, but are not limited to, suitable transformation or transfection formats, suitable transformation or transformation conditions, healthy host cell status, appropriate host cell density, and suitable cell culture environment. Suitable cell culture time. The “suitable conditions” are not particularly limited, and those skilled in the art can optimize the conditions for expression of the polypeptide according to the specific environment of the laboratory.
  • the invention provides a pharmaceutical composition.
  • the pharmaceutical composition comprises: a polypeptide as described above; and a pharmaceutically acceptable adjuvant.
  • the inventors have found through extensive experiments that a pharmaceutical composition comprising the aforementioned polypeptide and a pharmaceutically acceptable adjuvant can significantly stimulate the proliferation and secretion of CTL or TIL, and can significantly kill tumor cells presenting the above polypeptide antigen, with significant treatment or Prevention of tumors, especially the efficacy of tumors that specifically express the above polypeptide antigens.
  • the invention provides an antigen presenting cell.
  • the antigen presenting cell can present a polypeptide as described above.
  • the antigen presenting cell which presents the polypeptide described above is effective to cause an immune response of the patient against the tumor-specific antigen-the above polypeptide, thereby activating the CTL-specific killing function, and the antigen presenting according to the embodiment of the present invention Fine
  • the cells have remarkable efficacy in treating tumors expressing HLA-A0201 and the above polypeptides, and the therapeutic effect thereof is remarkable and the safety is high.
  • the antigen presenting cell is obtained by at least one of the following: contacting a cell having antigen presenting ability with the polypeptide; or the nucleic acid described above, or the nucleic acid construct described above Or the expression vector described above is introduced into the antigen-presenting cell.
  • the inventors have found through experiments that the antigen presenting cells can effectively present the polypeptide described above by any one or more of the above-mentioned methods, and expose the polypeptide described above to the surface of the presenting cell to present the antigen presenting of the aforementioned polypeptide.
  • the cells can effectively induce the patient's immune response to the tumor-specific antigen-the above polypeptide, thereby activating the CTL-specific killing function.
  • the antigen presenting cell is a dendritic cell.
  • Dendritic cells have strong antigen endocytosis and processing ability to present antigen on the surface of cells.
  • the inventors chose dendritic cells as antigen presenting cells, and antigen presenting cells initiate, regulate and maintain an immune response against the polypeptide in the body.
  • the invention provides an immune effector cell.
  • the immune effector cell can recognize the polypeptide described above or recognize an antigen presenting cell that presents the aforementioned polypeptide on the cell surface.
  • the immune effector cells are obtained by contacting the antigen presenting cells described above with cells having immunogenic effect.
  • the antigen presenting cell activates an immunogenic cell, activates the antigen, the aforementioned polypeptide, and activates
  • the cells having an immunogenic effect produce a large amount of immune effector cells, and the immune effector cells have a function of specifically killing the target cells which present the antigen-the polypeptide.
  • the cells having immunogenic effect ability are T lymphocytes, and the inventors have found that CD8 + T cells are preferred, and CD8 + T cells are more capable of undergoing antigen presenting cell activation, and CD8 + T obtained is obtained.
  • the specific killer of the cells presents the antigen - the target cells of the polypeptide are more potent.
  • the invention provides a vaccine.
  • the vaccine comprises a nucleic acid, a nucleic acid construct, an expression vector, a host cell, an antigen presenting cell as described above, or an immune effector cell as described above.
  • the nucleic acid, the nucleic acid construct, the expression vector, and the host cell of the embodiments of the present invention can be used for specific killing of a tumor highly expressing the polypeptide, and the antigen presenting cells proposed by the embodiments of the present invention have remarkable treatment.
  • the efficacy of the tumor expressing HLA-A0201 and the polypeptide, in addition, the immune effector cells proposed in the examples of the present invention have a significant specific killing effect on the antigen-presenting target cells of the polypeptide.
  • the vaccine according to the embodiment of the present invention comprises the nucleic acid, the nucleic acid construct, the expression vector, the host cell, the antigen presenting cell or the immune effector cell as described above, which has significant treatment or prevention of a tumor expressing HLA-A0201 and the polypeptide. Its role is to be safer and have fewer side effects.
  • the invention provides an antibody.
  • the antibody specifically recognizes a polypeptide as described above.
  • the antibody proposed in the embodiments of the present invention can specifically bind to the polypeptide, and can specifically recognize tumor cells which specifically express the polypeptide, and the antibody proposed in the embodiment of the invention plays a huge role in tumor diagnosis, treatment or prevention. effect.
  • the antibody can be obtained by collecting serum of an animal immunized with the polypeptide described above; and purifying the antibody of interest from the serum.
  • the polypeptide proposed in the embodiment of the present invention has higher specificity and higher specificity of the immune response because it is only found in the tumor tissue of the patient, and there is no normal tissue, and other tumor polypeptide vaccines. Compared with the advantages of being safer, having fewer side effects, and rarely causing a serious immune reaction, and because of its simple structure and easy artificial synthesis, it can be used as a vaccine, a pharmaceutical composition, etc., to cause an immune response against a tumor.
  • a polypeptide having the sequence of SEQ ID NO: 1 or a variant thereof can be used as a target or vaccine for tumor biological therapy directed against simultaneous expression of HLA-A0201 and the mutant polypeptide, having an immune response.
  • cancer including lung cancer, melanoma, breast cancer expressing the polypeptide sequence , nasopharyngeal cancer, liver cancer, stomach cancer, esophageal cancer, colorectal cancer, pancreatic cancer, skin cancer, prostate cancer, cervical cancer, leukemia, brain tumors and other cancer types, especially breast cancer.
  • the present invention proposes a method of treatment.
  • the method of treatment comprises: administering to the patient a therapeutically effective amount of a polypeptide as described above, a nucleic acid as described above, a nucleic acid construct as described above, an expression vector as described above, as described above Host cell, a pharmaceutical composition as described above, an antigen presenting cell as described above, an immune effector cell as described above, a vaccine as described above or an antibody as described above.
  • the therapeutic method proposed in the examples of the present invention comprises administering any effective amount of the aforementioned polypeptide or the like to effectively treat or prevent a tumor expressing HLA-A0201 and the polypeptide.
  • administering refers to introducing a predetermined amount of a substance into a patient in some suitable manner.
  • the polypeptide, nucleic acid, nucleic acid construct, expression vector, host cell, pharmaceutical composition, antigen presenting cell, immune effector cell, vaccine or antibody in the embodiments of the present invention can be administered by any common route as long as it can reach the expected organization.
  • Various modes of administration are contemplated, including peritoneal, venous, muscular, subcutaneous, cortical, oral, topical, nasal, pulmonary, and rectal, but the invention is not limited to these exemplary modes of administration.
  • the active ingredient of the orally administered composition should be coated or formulated to prevent its degradation in the stomach.
  • the compositions of the invention may be administered in an injectable preparation.
  • the pharmaceutical compositions of the invention may be administered using a particular device that delivers the active ingredient to the target cells.
  • the frequency and dose of administration of the polypeptide, nucleic acid, nucleic acid construct, expression vector, host cell, pharmaceutical composition, antigen presenting cell, vaccine or antibody in the embodiments of the present invention can be determined by a plurality of related factors, including The type of disease being treated, the route of administration, the age of the patient, the sex, the severity of the body weight and the disease, and the type of drug as the active ingredient.
  • the daily dose may be divided into 1 dose, 2 doses or multiple doses in a suitable form for administration once, twice or more times throughout the time period, as long as a therapeutically effective amount is achieved. .
  • treatment refers to an amount sufficient to significantly ameliorate certain symptoms associated with a disease or condition, that is, an amount that provides a therapeutic effect for a given condition and dosage regimen.
  • treatment is used to mean obtaining the desired pharmacological and/or physiological effect.
  • treatment encompasses the administration of a polypeptide, nucleic acid, nucleic acid construct, expression vector, host cell, pharmaceutical composition, antigen presenting cell, immune effector cell, vaccine or antibody in an embodiment of the invention to a subject for treatment, including but not It is limited to those individuals in need of administration as described herein.
  • the present invention proposes a diagnostic method.
  • the diagnostic method comprises: detecting whether the biological sample from which the patient is derived carries the polypeptide as described above; determining whether the patient has a tumor based on whether the biological sample carries the polypeptide. Since the polypeptide proposed in the embodiment of the present invention is only found in cancer tissues, the free polypeptide present in the serum can be detected by mass spectrometry, and the polypeptide is used as a tumor marker in the diagnosis of cancer to determine whether the patient has a disease. cancer. The inventors have found that the polypeptide is specifically highly expressed in tumor tissues, and the diagnostic method proposed in the examples of the present invention can effectively diagnose tumor patients that specifically express the polypeptide.
  • lung cancer melanoma
  • breast cancer nasopharyngeal cancer
  • liver cancer stomach cancer
  • esophageal cancer colorectal cancer
  • pancreatic cancer skin cancer, prostate cancer, cervical cancer, leukemia or brain tumors, especially breast cancer.
  • the polypeptide is specifically expressed in a highly specific manner, and further, the method according to the embodiment of the present invention further improves the diagnostic accuracy of the above tumor.
  • HLA-A0201 has a high proportion in the Chinese population, and thus, the diagnosis proposed by the embodiment of the present invention
  • the method has a higher probability of diagnosing a tumor patient who simultaneously expresses HLA-A0201 and the polypeptide.
  • the diagnostic system includes: a polypeptide detecting device 100; a diagnostic result determining device 200.
  • the polypeptide detecting device 100 is configured to detect whether the biological sample derived from the patient carries the polypeptide described above, and the diagnostic result determining device 200 is connected to the polypeptide detecting device 100 for determining whether the biological sample carries the polypeptide. Whether the patient has a tumor.
  • the free peptide present in the serum of the patient may be detected by a mass spectrometer, and then the presence or absence of the free polypeptide in the serum of the patient is determined by a mass spectrometry data analysis device to determine whether the patient has a tumor.
  • a mass spectrometry data analysis device to determine whether the patient has a tumor.
  • lung cancer melanoma
  • breast cancer nasopharyngeal cancer
  • liver cancer gastric cancer
  • esophageal cancer colorectal cancer
  • pancreatic cancer skin cancer, prostate cancer, cervical cancer, leukemia or brain tumors, especially breast cancer.
  • the specificity of the polypeptide is highly expressed, and the diagnostic system proposed by the embodiment of the present invention further improves the diagnostic accuracy of the above tumor.
  • HLA-A0201 has a high proportion in the Chinese population, and HLA-A0201 has a strong affinity with the polypeptide, and the polypeptide stimulates a series of immune responses by binding to the cell surface HLA-A0201. .
  • the diagnostic system proposed by the embodiments of the present invention diagnoses a tumor patient who simultaneously expresses HLA-A0201 and the polypeptide with a higher probability.
  • the polypeptide according to the embodiment of the present invention and the use thereof, the nucleic acid encoding the polypeptide, the nucleic acid construct, the expression vector, the host cell, the pharmaceutical composition, the antigen presenting cell, the immune effector cell, the vaccine, the antibody, the treatment The method and system for diagnosing cancer are discovered and completed by the inventor of the present application after painstaking creative labor and optimization work.
  • the affinity prediction of the polypeptides was separately performed using the self-developed "tumor DNA and RNA sequencing-based mutant polypeptide binding ability prediction software" (software copyright number: 2016SR002835). Results are expressed as the predicted IC 50 value, IC 50 less than 500nM indicates that the affinity polypeptide, IC 50 of less than 50nM represents the polypeptide with high affinity.
  • the inventors predicted the affinity of the wild type (ILVDWLVEV (SEQ ID NO: 5)) polypeptide, the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) and its variable forms (SEQ ID NO: 2-4) polypeptides, and finally screened the mutant polypeptide.
  • ILVDWLFEV (SEQ ID NO: 1) 1.57 ILVDWLVEV (SEQ ID NO: 5) 7.68 IMVDWLFEL (SEQ ID NO: 2) 2.01 ILVDWLVEV (SEQ ID NO: 5) 7.68 ILVDWLFEL (SEQ ID NO: 3) 1.89 ILVDWLVEV (SEQ ID NO: 5) 7.68 IMVDWLFEV (SEQ ID NO: 4) 1.72 ILVDWLVEV (SEQ ID NO: 5) 7.68
  • the IC 50 of the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) and its variable form (SEQ ID NO: 2-4) polypeptides were all predicted to be less than 50 nM, indicating that the mutant polypeptide and its variable form polypeptide were predicted, All are high affinity polypeptides. Polypeptide and its mutant form of the polypeptide of the variable is less than the wild type IC 50 (ILVDWLVEV (SEQ ID NO: 5 )) polypeptide. Thus, it is predicted that the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) and its variable form (SEQ ID NO: 2-4) polypeptides have higher affinity than the wild type (ILVDWLVEV (SEQ ID NO: 5)) polypeptide.
  • polypeptides involved in the examples of the invention were synthesized according to standard solid phase synthesis methods and purified by reverse phase HPLC. The purity (>90%) and identity of the polypeptide were determined by HPLC and mass spectrometry, respectively.
  • T2 cells are HLA-A2-positive T and B lymphocyte hybridoma cells, which can express HLA-A0201 on the cell surface, but cannot be transported due to defects in the essential antigen polypeptide transporter (TAP) in the endogenous antigen presentation pathway. Endogenous antigen. T2 cells were purchased from ATCC (number: CRL-1992).
  • T2 cells were purchased from ATCC (number: CRL-1992).
  • T2 cells 2 ⁇ 10 5 T2 cells were taken and resuspended in a 24-well plate with 500 ⁇ l of IMDM serum-free medium containing human ⁇ 2 microglobulin (final concentration, 3 ⁇ g/ml), and synthetic wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide, ILVDWLFEV (SEQ ID NO: 1) polypeptide or three variable forms thereof (SEQ ID NO: 2 to 4) polypeptide (final concentration 100 ⁇ M), cultured in an incubator (37 ° C, 5% CO 2 ) overnight. Two replicate wells per group; T2 cells without polypeptide added were used as background controls, and CMV polypeptide (NLVPMVATV (SEQ ID NO: 6)) was added as a positive control.
  • the cells were collected by centrifugation of 200 g of cells for 5 minutes. After the cells were washed twice with PBS, the cells were directly incubated with anti-HLA-A*02:01 FITC monoclonal antibody and maintained at 4 ° C for 30 minutes.
  • flow cytometry BD FACSJazz TM software to detect and analyze their mean fluorescence intensity.
  • FI>1.5 indicates that the peptide has high affinity for HLA-A*0201 molecule
  • 1.0 ⁇ FI ⁇ 1.5 indicates that the peptide has moderate affinity for HLA-A*02:01 molecule
  • 0.5 ⁇ FI ⁇ 1.0 indicates that the peptide is HLA-A*0201 molecule has low affinity.
  • ILVDWLVEV (SEQ ID NO: 5) 100 ⁇ M 441 2.13 High affinity ILVDWLFEV (SEQ ID NO: 1) 100 ⁇ M 385 1.73 High affinity IMVDWLFEL (SEQ ID NO: 2) 100 ⁇ M 410 1.91 High affinity ILVDWLFEL (SEQ ID NO: 3) 100 ⁇ M 389 1.76 High affinity IMVDWLFEV (SEQ ID NO: 4) 100 ⁇ M 418 1.96 High affinity Background control 0 ⁇ M 141 0.00 No affinity CMV positive control 100 ⁇ M 658 1.87 High affinity
  • PBMC Peripheral blood mononuclear cells
  • Ficoll lymphocyte separation solution was used to separate peripheral blood mononuclear cells (PBMC).
  • PBMCs were used to attach mononuclear cells, and CD8 magnetic beads were used to screen PBMCs.
  • GM-CSF 1000 U/ml
  • IL-4 1000 U/ml
  • IFN-gamma 100 U/ml
  • LPS 10 ng/ml
  • mutant polypeptide ILVDWLFEV SEQ ID NO: 1
  • mutant polypeptide ILVDWLFEV SEQ ID NO: 2
  • mutant polypeptide ILVDWLFEV SEQ ID NO: 3
  • mutant polypeptide ILVDWLFEV SEQ ID NO: 4
  • mutant polypeptide ILVDWLFEV SEQ ID NO: 2-4
  • the mature DC cells loaded with the polypeptide were co-cultured with CD8 + T cells of the volunteers, and IL-21 was added. After 3 days, IL-2 and IL-7 were added, and then IL-addition was performed on the 5th and 7th days. 2 and IL-7, co-cultured cells were counted on day 10, and subsequent ELISPOTs and LDH assays. The result of the counting is shown in Table 3:
  • ILVDWLVEV SEQ ID NO: 5
  • ILVDWLVEV SEQ ID NO: 5
  • ILVDWLFEV SEQ ID NO: 1
  • IMVDWLFEL SEQ ID NO: 2
  • ILVDWLFEL SEQ ID NO: 3
  • 2.0 ⁇ 10 6 6.9 ⁇ 10 6 IMVDWLFEV SEQ ID NO: 4
  • Example 3 The cells co-cultured in Example 3 were separately cultured and detected with T2 cells loaded with the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) and wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide into human interferon-gamma ELISPOTs plates. The spots produced by the ELISPOT experiment were finally counted.
  • the requirement for immunogenicity of the mutant polypeptide is as follows: the number of spots (mutant polypeptide) / number of spots (wild type) polypeptide > 2, that is, the number of spots caused by the mutant polypeptide exceeds twice the number of spots of the wild type polypeptide, and the polypeptide has an immunogen. Sexual requirements.
  • CD8 + T cells can specifically recognize the complex of HLA-A0201 and polypeptide, the difference in polypeptide sequence, and the T cell population of the complex of recognition polypeptide and HLA-A0201 are also different. Since T2 cells express HLA-A0201, CD8 + T cells are able to specifically recognize T2 cells loaded with the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1), but not the wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide load. T2 cells. After specifically recognizing the complex of HLA-A0201 and the polypeptide, the polypeptide-specific CD8 + T cells can reactivate and secrete IFN-gamma interferon.
  • ILVDWLFEV mutant polypeptide ILVDWLFEV
  • SEQ ID NO: 5 wild-type ILVDWLVEV
  • the IFN-gamma interferon secreted by CD8 + T cells can be captured by antibodies on the ELISPOTs plate.
  • the antibody that finally recognizes IFN-gamma can catalyze the coloration of the substrate through the enzyme coupled to the antibody, eventually producing spots. .
  • the number of spots represents the number of cells that are activated to secrete IFN-gamma interferon.
  • Example 5 LDH release assay demonstrates CD8 + T cell killing activity
  • Example 3 The cells co-cultured in Example 3 were separately loaded with the over-mutated polypeptide ILVDWLFEV (SEQ ID NO: 1) or its three variable form polypeptides (SEQ ID NOS: 2-4), wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide.
  • T2 cells without polypeptide loading were co-cultured, and the largest release well, volume correction well, medium control well, spontaneous release well, and different target ratio (ie, effector cells (T cells) and target cells (T2 cells) were set in the experiment. The number of cells was compared with each other. Three replicate wells were set in each group.
  • the formula for calculating the killing activity is:
  • Killing efficiency (experimental well-effect cell spontaneous release - target cell spontaneous release + medium well) / (target cell maximum release - volume correction hole - target cell spontaneous release + medium well) ⁇ 100%
  • lactate dehydrogenase is one of the enzymes contained in the cytoplasm of living cells, and under normal conditions, it cannot penetrate the cell membrane.
  • LDH lactate dehydrogenase
  • the released LDH converts oxidized coenzyme I (NAD+) into reduced coenzyme I (NADH) during the catalysis of lactic acid to produce pyruvate, which is then passed through the hydrogen donor-phenazine dimethyl sulfate (PMS).
  • T cells specifically recognize and kill target cells loaded with experimental peptides
  • the mutant polypeptide and its variable form polypeptide-activated T cells were able to kill the mutant polypeptide ILVDWLFEV (SEQ ID NO: at a target ratio of 1:1 or 10:1). 1) or its three variable form polypeptides (SEQ ID NOS: 2 to 4) T2 cells, but not T2 cells carrying the wild-type polypeptide ILVDWLVEV (SEQ ID NO: 5), which further validates the activation of the experimental group polypeptide (polypeptide of the amino acid sequence shown in SEQ ID NO: 1 and its variable form polypeptide) T cells are capable of specifically killing target cells carrying the mutant polypeptide ILVDWLFEV (SEQ ID NO: 1) or its three variable form polypeptides (SEQ ID NOS: 2-4).
  • Example 6 Establishment of a subcutaneous xenograft model of a MCF7-ILVDWLFEV (SEQ ID NO: 1) polypeptide or a variant polypeptide thereof
  • the DNA sequence of the synthetic ILVDWLFEV (SEQ ID NO: 1) polypeptide is set forth in SEQ ID NO: 7, TATTCTTCTCCTACTTCAACTAACCAG (SEQ ID NO: 7),
  • DNA sequence of the variable form IMVDWLFEL (SEQ ID NO: 2) polypeptide is set forth in SEQ ID NO: 8, TATATGTCTCCTACTTCAACTAACTTA (SEQ ID NO: 8),
  • variable form ILVDWLFEL SEQ ID NO: 3
  • TATTCTTCTCCTACTTCAACTAACTTA SEQ ID NO: 9
  • polypeptide DNA sequence of its variable form IMVDWLFEV (SEQ ID NO: 4) is set forth in SEQ ID NO: 10, TATATGTCTCCTACTTCAACTAACCAG (SEQ ID NO: 10),
  • the DNA sequence corresponding to the wild type ILVDWLVEV (SEQ ID NO: 5) polypeptide is shown in SEQ ID NO: 11, TATTCTTCTCCTACTTCAGTCAACCAG (SEQ ID NO: 11).
  • the lentiviral vector pHBLV-Puro expressing the polypeptide of the wild type polypeptides ILVDWLVEV (SEQ ID NO: 5), ILVDWLFEV (SEQ ID NO: 1) and their variable form polypeptides, respectively, was constructed. They are named pHBLV-Puro-ILVDWLVEV, pHBLV-Puro-ILVDWLFEV, pHBLV-Puro-IMVDWLFEL, pHBLV-Puro-ILVDWLFEL, pHBLV-Puro-IMVDWLFEV, respectively.
  • the 5 lentiviral plasmids were co-transfected into 293T cells together with pSPAX2 and pMD2G helper plasmids, and the wild type polypeptides ILVDWLVEV (SEQ ID NO: 5) and ILVDWLFEV (SEQ ID NO: 1) were expressed. Lentiviruses of variant polypeptides (SEQ ID NOS: 2 to 4).
  • the human breast cancer cell line MCF7 was purchased from ATCC (number: HTB-22) and its HLA subtype was HLA-A*0201 positive.
  • the cells were cultured in DMEM medium containing 10% fetal calf serum, 100 U/mL penicillin and streptomycin. Incubate in a 37 ° C, 5% CO 2 incubator.
  • the packaged ILVDWLFEV (SEQ ID NO: 1) lentivirus was transfected into the MCF7 cell line, and the surviving MCF7 cell line was continuously screened with the Puromycin antibiotic (puromycin) to finally establish the expression of the ILVDWLFEV (SEQ ID NO: 1) polypeptide.
  • MCF7 cell line It can be named as MCF7-ILVDWLFEV (SEQ ID NO: 1) cell line.
  • PBMC peripheral blood mononuclear cells
  • NOD SCID mice Thirty-six NOD SCID mice were excluded from the immune leak, and each of the NOD SCID mice was subjected to human immune reconstitution by intraperitoneal injection of PBMC 2 ⁇ 10 7 /0.5 ml. Further, mice selected after 4 weeks were prepared to inoculate a human breast cancer cell line model.
  • MCF7-ILVDWLFEV The established human breast cancer cell line MCF7-ILVDWLFEV (SEQ ID NO: 1) was cultured in DMEM medium containing 10% fetal calf serum, 100 U/mL penicillin and streptomycin. Incubate in a 37 ° C, 5% CO 2 incubator. MCF7-ILVDWLFEV (SEQ ID NO: 1) tumor cells were collected, centrifuged at 3000 rpm, and the tumor cells were washed 3 times with sterile physiological saline. Dilute appropriately, take 40 ⁇ l of cell suspension and add 10 ⁇ l of 0.4% phenol blue staining and microscopically count to make a tumor cell suspension with a concentration of 1 ⁇ 10 8 /ml, and select NOD/ after immune reconstruction.
  • the MCF7-ILVDWLFEV (SEQ ID NO: 1) subcutaneous tumor model NOD/SCID mice immunized for 4 weeks were subjected to polypeptide + complete Freund's adjuvant vaccine, or polypeptide + DC vaccine, or lentivirus-infected DC cell vaccine, As well as DC-CTL vaccine treatment, the tumor volume and mouse survival rate were recorded every 2 days.
  • the MCF7-ILVDWLFEV (SEQ ID NO: 1) subcutaneous tumor model NOD/SCID mice immunized for 4 weeks were randomly divided into 6 groups: adjuvant + wild type ILVDWLVEV (SEQ ID NO: 5) polypeptide group, adjuvant group, Adjuvant ten ILVDWLFEV (SEQ ID NO: 1) group or three variable form polypeptide groups of 6 each.
  • the first immunization dose of the wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide, the ILVDWLFEV (SEQ ID NO: 1) polypeptide, and the three variant form polypeptides thereof was 100 ⁇ g/head.
  • the polypeptide was resuspended in PBS, mixed with 150 ⁇ l of Freund's complete adjuvant, adjusted to 300 ⁇ l/cell with PBS, and injected subcutaneously at the back. After 2 weeks, the same dose was used for booster immunization (the first use of complete Freund's adjuvant, followed by incomplete Freund's adjuvant), and a total of 4 immunizations.
  • the general characteristics of the mice were observed daily, including mental state, activity, response, diet, body weight, and tumor growth. The longest diameter (long) and shortest diameter (width) of the tumor were measured with a vernier caliper every 2 days.
  • the calculation formula of tumor volume is: 1/2 ⁇ length ⁇ width 2 ;
  • the results are shown in Figure 5.
  • PBMC peripheral blood mononuclear cells
  • ILVDWLVEV wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide, ILVDWLFEV (SEQ ID NO: 1) polypeptide and three variable form polypeptides thereof (concentration: 10 ⁇ g/ml), inducing adherent monocytes into mature DC cells, harvesting Mature DC was washed 3 times with physiological saline. After loading with physiological saline DC polypeptide is adjusted to (4.0 ⁇ 0.5) ⁇ 10 7 / ml, for subsequent experiments.
  • mice were randomized into 5 groups: DC-loaded wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide group, DC-loaded ILVDWLFEV (SEQ ID NO: 1) polypeptide, and DC-loaded 3 variability forms (SEQ ID NO: 2-4) Polypeptide group, 6 in each group.
  • a DC-loaded wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide, a DC-loaded ILVDWLFEV (SEQ ID NO: 1) polypeptide, and a variable form of a polypeptide cell suspension of any of the same are prepared.
  • the inner side of the thigh of the mouse was intradermally injected, 0.1 ml per side, and once a week.
  • DC vaccine can significantly prolong the survival of mice and slow the growth of tumors in mice.
  • PBMC peripheral blood mononuclear cells
  • PBMC cells were harvested, incubated at 37 ° C for 2 h, washed away unattached cells, recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF), recombination Human white medium-4 (rhIL-4) cultured DC cells.
  • rhGM-CSF granulocyte-macrophage colony-stimulating factor
  • rhIL-4 recombination Human white medium-4
  • SEQ ID NO: 1 Lentiviral fluid of the polypeptide and its variable form polypeptide.
  • the virus culture solution was removed, and a culture medium containing 50 ng/ml rhIL-4, 100 ng/ml rh GM-CSF, 100 U/ml IFN- ⁇ and 100 ng/ml LPS was added and placed in a 37 ° C 5% CO 2 incubator. Cultivate.
  • lentivirus-infected DC cells were observed under a fluorescence microscope, and mature DC cells were collected for treatment of mouse tumor model. The cells were washed 3 times with physiological saline, and the DC was adjusted to (4.0 ⁇ 0.5) x 10 7 / ml for subsequent experiments.
  • mice were randomized into 5 groups: wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide-DC group, ILVDWLFEV (SEQ ID NO: 1) polypeptide-DC group, and three variability forms thereof (SEQ ID NO: 2)
  • the polypeptide-DC group shown in any of the ⁇ 4 sequences, was 6 in each group.
  • the inner side of the thigh of the mouse was intradermally injected, 0.1 ml per side, and once a week.
  • the dose was (4.0 ⁇ 0.5) ⁇ 10 6 cells / time, a total of 2 injections.
  • the vital signs of the mice were observed, and the vertical and horizontal dimensions of the tumors were measured with vernier calipers every 2 days.
  • the changes in body weight and survival of the mice were recorded. The result is shown in Figure 7.
  • the results show that the polypeptide gene of the ILVDWLFEV (SEQ ID NO: 1) polypeptide or its variable form (shown in any of SEQ ID NO: 2 to 4) is expressed relative to the wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide control group.
  • the packaged lentiviral-infected DC vaccine has significant tumor suppressive effects and can significantly prolong the survival of mice.
  • ILVDWLFEV ILVDWLFEV
  • the cells were harvested on the 7th day after the third stimulation, which is cytotoxic T lymphocytes (CTL).
  • CTL cytotoxic T lymphocytes
  • the cells were resuspended in physiological saline, resuspended in a volume of 0.2 ml, and returned via the tail vein.
  • the number of cells per mouse in each tumor model was about 1 ⁇ 10 8 cells.
  • the vital signs of the mice were observed and the vertical and horizontal dimensions of the tumors were measured with vernier calipers every 2 days. The result is shown in Figure 8.
  • the results show that the ILVDWLFEV (SEQ ID NO: 1) polypeptide or its variable form (shown in any of SEQ ID NOs: 2 to 4) polypeptide is activated relative to the wild-type ILVDWLVEV (SEQ ID NO: 5) polypeptide control group.
  • the DC-CTL vaccine has a significant tumor suppressive effect and can significantly prolong the survival of mice.
  • the polypeptide of the present invention can be effectively applied to the preparation of a kit, a drug or a vaccine, and the specificity of the immune reaction caused by the drug or vaccine is also higher, and it is safer and has fewer side effects than other tumor polypeptide vaccines. It has the advantages of less serious immune reaction, and because of its simple structure and easy artificial synthesis, it can be used as a vaccine, a pharmaceutical composition, etc., to cause an immune response against a tumor.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Microbiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Zoology (AREA)
  • Mycology (AREA)
  • Wood Science & Technology (AREA)
  • Biotechnology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Oncology (AREA)
  • Plant Pathology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

L'invention concerne un polypeptide, un acide nucléique codant pour le polypeptide, une construction d'acide nucléique comprenant l'acide nucléique, un vecteur d'expression, une cellule hôte, et une cellule de présentation d'antigène présentant le polypeptide sur la surface de la cellule, ainsi qu'une cellule effectrice immunitaire de celle-ci, une composition pharmaceutique, un vaccin et un anticorps comprenant le polypeptide, un procédé thérapeutique, un procédé de diagnostic et un dispositif de diagnostic, et l'utilisation du polypeptide dans la préparation d'un vaccin, un kit de diagnostic de tumeur ou une composition pharmaceutique, et l'utilisation du polypeptide et de l'acide nucléique servant de cibles de détection dans le diagnostic de tumeurs.
PCT/CN2016/108102 2016-11-30 2016-11-30 Polypeptide et son application Ceased WO2018098715A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
PCT/CN2016/108102 WO2018098715A1 (fr) 2016-11-30 2016-11-30 Polypeptide et son application
CN201680090579.2A CN110167956B (zh) 2016-11-30 2016-11-30 多肽及其应用

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2016/108102 WO2018098715A1 (fr) 2016-11-30 2016-11-30 Polypeptide et son application

Publications (1)

Publication Number Publication Date
WO2018098715A1 true WO2018098715A1 (fr) 2018-06-07

Family

ID=62240982

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2016/108102 Ceased WO2018098715A1 (fr) 2016-11-30 2016-11-30 Polypeptide et son application

Country Status (2)

Country Link
CN (1) CN110167956B (fr)
WO (1) WO2018098715A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113444149A (zh) * 2020-03-18 2021-09-28 北京鼎成肽源生物技术有限公司 一种乳腺癌靶标抗原、乳腺癌靶标抗原刺激培养的ctl细胞及其应用
CN114409744A (zh) * 2022-03-29 2022-04-29 深圳吉诺因生物科技有限公司 Hpv抗原表位及其鉴定方法、应用

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1261374A (zh) * 1997-06-23 2000-07-26 路德维格癌症研究所 结合hla分子的分离的九肽和十肽及其应用
WO2004031345A2 (fr) * 2002-05-20 2004-04-15 The General Hospital Corporation Épitopes de lymphocytes t cytotoxiques du virus vih-1
CN101424691A (zh) * 2008-12-15 2009-05-06 北京大学第三医院 浸润性乳腺癌复发风险评估试剂盒
CN101508721A (zh) * 2009-03-24 2009-08-19 中国人民解放军第三军医大学 肿瘤抗原Ran HLA-A*0201限制性模拟CTL表位及其应用
CN102905721A (zh) * 2010-03-19 2013-01-30 伊玛提克斯生物技术有限公司 基于avl9的癌症的诊断及治疗
US20170037107A1 (en) * 2015-07-01 2017-02-09 Immatics Biotechnologies Gmbh Novel peptides and combination of peptides for use in immunotherapy against ovarian cancer and other cancers

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7928190B2 (en) * 2007-07-05 2011-04-19 Darnell Robert B Methods and compositions for tumor vaccination and therapy
JP5267969B2 (ja) * 2007-12-04 2013-08-21 学校法人慶應義塾 癌ワクチン
CN104914242B (zh) * 2014-09-29 2017-08-11 深圳华大基因科技服务有限公司 用于癌症诊断和治疗的方法和组合物

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1261374A (zh) * 1997-06-23 2000-07-26 路德维格癌症研究所 结合hla分子的分离的九肽和十肽及其应用
WO2004031345A2 (fr) * 2002-05-20 2004-04-15 The General Hospital Corporation Épitopes de lymphocytes t cytotoxiques du virus vih-1
CN101424691A (zh) * 2008-12-15 2009-05-06 北京大学第三医院 浸润性乳腺癌复发风险评估试剂盒
CN101508721A (zh) * 2009-03-24 2009-08-19 中国人民解放军第三军医大学 肿瘤抗原Ran HLA-A*0201限制性模拟CTL表位及其应用
CN102905721A (zh) * 2010-03-19 2013-01-30 伊玛提克斯生物技术有限公司 基于avl9的癌症的诊断及治疗
US20170037107A1 (en) * 2015-07-01 2017-02-09 Immatics Biotechnologies Gmbh Novel peptides and combination of peptides for use in immunotherapy against ovarian cancer and other cancers

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
KUHNE, C. ET AL.: "A New Pair of B-Type Cyclins from Saccharomyces cerevisiae that Function Early in the Cell Cycle", THE EMBO JOURNAL, vol. 12, no. 9, 31 October 1993 (1993-10-31), pages 3437 - 3447, XP055509034 *
MITTENDORF, E. A. ET AL.: "Breast Cancer Cell Uptake of the Inflammatory Mediator Neutrophil Elastase Triggers an Anti-Cancer Adaptive Immune Response", CANCER RESEARCH, vol. 72, no. 13, 1 July 2013 (2013-07-01), pages 3153 - 3162, XP055509029 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113444149A (zh) * 2020-03-18 2021-09-28 北京鼎成肽源生物技术有限公司 一种乳腺癌靶标抗原、乳腺癌靶标抗原刺激培养的ctl细胞及其应用
CN114409744A (zh) * 2022-03-29 2022-04-29 深圳吉诺因生物科技有限公司 Hpv抗原表位及其鉴定方法、应用
WO2023184861A1 (fr) * 2022-03-29 2023-10-05 深圳吉诺因生物科技有限公司 Épitope de hpv, son procédé d'identification et son utilisation

Also Published As

Publication number Publication date
CN110167956A (zh) 2019-08-23
CN110167956B (zh) 2023-04-07

Similar Documents

Publication Publication Date Title
TWI838465B (zh) 腫瘤免疫治療多肽及其應用
CN109923121B (zh) 多肽及其应用
CN110214144B (zh) 多肽及其应用
US11213563B2 (en) Polypeptide and use thereof
US11548925B2 (en) CACNA1H-derived tumor antigen polypeptide and use thereof
US11142547B2 (en) Polypeptide and use thereof
CN110167956B (zh) 多肽及其应用
TWI748349B (zh) 腫瘤特異性多肽序列及其應用
US11820836B2 (en) Polypeptide and use thereof
US11612643B2 (en) Col14A1-derived tumor antigen polypeptide and use thereof
CN110072876B (zh) 多肽及其应用
US11396528B2 (en) Polypeptide and use thereof
WO2018032501A1 (fr) Nouveau polypeptide spécifique de tumeur et son application
HK40010123B (zh) 多肽及其应用
HK40010534B (en) Polypeptide and application thereof
HK40010120B (en) Polypeptide and application thereof
HK40010120A (en) Polypeptide and application thereof
HK40010104B (en) Polypeptide and application thereof
HK40002414B (en) Polypeptide and application thereof
HK40002414A (en) Polypeptide and application thereof
HK40010495B (en) Col14a1-derived tumour antigen polypeptide and use thereof
HK40010123A (en) Polypeptide and application thereof
HK40010104A (zh) 多肽及其应用
HK40010534A (en) Polypeptide and application thereof

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16922776

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16922776

Country of ref document: EP

Kind code of ref document: A1