已公布的胃癌抗原清单

肿瘤新抗原mRNA疫苗在加速审批的背景下,肿瘤突变抗原的研究价值越来越大,为此,我们通过文献挖掘,为读者整理了各种肿瘤的已验证肿瘤突变抗原清单,我们将陆续发布

以下是目前公布的胃癌肿瘤抗原肽清单,该清单均支持定制生产 (定制咨询请扫描本页右侧联系人二维码)。可定制生产:

  1. 检测或分选抗原特异性T细胞的流式试剂、磁珠分选试剂
  2. 构建抗原肽和MHC复合物,用于合成人工呈递物,从而刺激T细胞增殖

胃癌抗原蛋白的抗原肽数量分布

Antigen NameDescriptionAllele Namepaper
Protein E7YMLDLQPETTHLA-A*02:01Occasional memory cytotoxic T-cell responses of patients with human papillomavirus type 16-positive cervical lesions against a human leukocyte antigen-A *0201-restricted E7-encoded epitope. Cancer Res 1996
Squamous cell carcinoma antigen recognized by T-cells 3VYDYNCHVDLHLA-A*24:02Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Squamous cell carcinoma antigen recognized by T-cells 3AYIDFEMKIHLA-A*24:02Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Tyrosine-protein kinase LckDYLRSVLEDFHLA-A*24:02Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Peptidyl-prolyl cis-trans isomerase BVLEGMEVVHLA-A2Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
lymphocyte-specific protein tyrosine kinaseKLVERLGAAHLA-A2Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Serine/threonine-protein kinase WNK2DLLSHAFFAHLA-A2Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Plasmanylethanolamine desaturaseRLQEWCSVIHLA-A2Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Dermatan-sulfate epimeraseDYSARWNEIHLA-A*24:02Immunological evaluation of vaccination with pre-designated peptides frequently selected as vaccine candidates in an individualized peptide vaccination regimen. Int J Oncol 2004
Prostatic acid phosphataseLYCESVHNFHLA-A*24:02Prostatic acid phosphatase as a target molecule in specific immunotherapy for patients with nonprostate adenocarcinoma. J Immunother 2005
Claudin-18YTFGAALFVHLA-A*02:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18GLLVSIFALHLA-A*02:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18TLTSGIMFIHLA-A*02:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18GLPAMLQAVHLA-A*02:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18TLTSGIMFIVHLA-A*02:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18STGFGSNTKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18LLVSIFALKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18VAYKPGGFKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18SVAYKPGGFKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18HASGHSVAYKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022
Claudin-18GLLVSIFALKHLA-A*11:01Antigen-Specific T Cell Immunotherapy Targeting Claudin18.2 in Gastric Cancer. Cancers (Basel) 2022

重点说明:Claudin-18作为靶点的在研药物有70多种进入临床试验,该靶点是胃癌领域的热点研发领域。其中,CLDN18.2是研究最为透彻的CLDN18蛋白成员。

CLDN18.2通常存在于胃黏膜细胞的紧密连接处,维持胃粘膜的屏障功能,防止胃酸的H+通过细胞旁路途径渗透。CLDN18.2在正常组织中表达有限,而在多种恶性肿瘤发展中异常表达,如胃癌/胃食管交界处癌症(GC/GEJ)、乳腺癌、结肠癌、肝癌、头颈癌、支气管癌和非小细胞肺癌。CLDN18.2参与肿瘤细胞的增殖、分化和迁移。癌组织的紧密连接被破坏,导致CLDN18.2结合表位暴露出来。

这使靶向的大分子药,比如抗体药物,甚至CAR-T细胞治疗药物更易与肿瘤部位的CLDN18.2结合,而不与正常组织中的CLDN18.2结合,减小毒副作用。

胃瘤抗原清单使用方法:

肿瘤微环境研究:

检测肿瘤浸润淋巴细胞中,肿瘤抗原特异性淋巴细胞的数量实现。具体方式是:根据清单内容,将抗原肽和HLA合成为抗原肽MHC复合物荧光四聚体,通过流式细胞检测方法,检测肿瘤浸润淋巴细胞的含量。

肿瘤免疫细胞的全身分布:

通过检测外周血中肿瘤抗原特异性淋巴细胞的数量实现。具体方法同上。

过继性肿瘤免疫细胞治疗:

使用清单中抗原肽,刺激淋巴细胞,而后使用抗原肽MHC复合物荧光四聚体或磁珠四聚体,通过流式分选或磁珠分选细胞,经体外细胞增殖后,回输体内,评估肿瘤抑制效果。

肿瘤抗原特异性TCR测序:

通过肿瘤浸润淋巴细胞、或外周血淋巴细胞,通过分选后进行单细胞TCR测序,获得抗原特异性T细胞的TCR序列,进一步进行TCR-T疗法研究。

肿瘤疫苗片段筛选:

综合上述过程,获得具有激活T细胞杀伤肿瘤细胞的经验证抗原肽MHC复合物,用于肿瘤疫苗构建。

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