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    • 2. 发明申请
    • PROSTATE-SPECIFIC TUMOR ANTIGEN AND USES THEREOF
    • 前列腺特异性肿瘤抗原及其用途
    • WO2014047085A3
    • 2015-07-23
    • PCT/US2013060254
    • 2013-09-18
    • WANG RONGFU
    • WANG RONGFU
    • A61K39/00A61P35/00
    • A61K38/1703A61K38/193A61K39/0011A61K2300/00
    • Twenty-one PSGR-derived peptides predicted by an immuno-informatics approach based on the HLA-A2 binding motif were examined for their ability to induce peptide-specific T cell responses in peripheral blood mononuclear cells (PBMCs) obtained from either HLA-A2+ healthy donors or HLA-A2+ prostate cancer patients. The recognition of HLA-A2 positive and PSGR expressing LNCaP cells was also tested. Three peptides, PSGR3, PSGR4 and PSGR14 frequently induced peptide-specific T cell responses in PBMCs from both healthy donors and prostate cancer patients, and are recognized by CD8+ T cells in an HLA-A2 dependent manner. These peptide-specific T cells recognize HLA-A2+ and PSGR+ tumor cells, and killed LNCaP prostate cancer cells in an HLA class I-restricted manner. These PSGR-derived peptides identified are useful as diagnostic markers as well as immune targets for anticancer vaccines.
    • 检测了通过基于HLA-A2结合基序的免疫信息学方法预测的21种PSGR衍生肽在从HLA-A2 +健康获得的外周血单核细胞(PBMC)中诱导肽特异性T细胞应答的能力 供体或HLA-A2 +前列腺癌患者。 还测试了表达HLA-A2阳性和PSGR的LNCaP细胞的识别。 三种肽,PSGR3,PSGR4和PSGR14经常诱导来自健康供体和前列腺癌患者的PBMC中的肽特异性T细胞应答,并且被CD8 + T细胞以HLA-A2依赖性方式识别。 这些肽特异性T细胞识别HLA-A2 +和PSGR +肿瘤细胞,并以HLA I类限制的方式杀死LNCaP前列腺癌细胞。 鉴定的这些PSGR衍生肽可用作抗癌疫苗的诊断标记物和免疫靶标。