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首页> 外文期刊>British Journal of Cancer >Identification of an HLA-A|[ast]|0201-restricted T-cell epitope derived from the prostate cancer-associated protein prostein
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Identification of an HLA-A|[ast]|0201-restricted T-cell epitope derived from the prostate cancer-associated protein prostein

机译:鉴定源自前列腺癌相关蛋白prostein的HLA-A | ast | 0201限制性T细胞表位

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The development of T-cell-based immunotherapies of cancer largely depends on the availability of tumour-associated antigens capable of eliciting tumour-directed cytotoxic T-cell responses. In prostate cancer, the number of antigens defined as suitable targets of cytotoxic T lymphocytes (CTLs) is still limited. Recently, prostein was identified as a transmembrane protein that is highly restricted to prostate tissues. In our study, prostein transcripts were found to be abundant in both malignant and nonmalignant prostate tissue samples. To identify immunogenic CD8+ T-cell epitopes, human leucocyte antigen-A*0201-binding peptides were selected from the amino-acid sequence of prostein and were used for the in vitro stimulation of CD8+ T lymphocytes. Specific CTLs were raised against the prostein-derived peptide CLAAGITYV that were capable of lysing prostate cancer cells, indicating that this peptide is naturally generated by tumour cells. Our data suggest that prostein is a suitable candidate to be included in a T-cell-based immunotherapy of prostate cancer.
机译:基于T细胞的癌症免疫疗法的发展很大程度上取决于能够引发肿瘤定向的细胞毒性T细胞反应的肿瘤相关抗原的可用性。在前列腺癌中,被定义为细胞毒性T淋巴细胞(CTL)的合适靶标的抗原数量仍然有限。最近,前列腺素被鉴定为高度限制前列腺组织的跨膜蛋白。在我们的研究中,发现前列腺素在恶性和非恶性前列腺组织样本中都丰富。为了鉴定具有免疫原性的CD8 + T细胞表位,从脯氨酸的氨基酸序列中选择人白细胞抗原-A * 0201结合肽,并将其用于体外刺激CD8 + T淋巴细胞。针对能够裂解前列腺癌细胞的前列腺素衍生肽CLAAGITYV产生了特异性CTL,表明该肽是肿瘤细胞天然产生的。我们的数据表明,前列腺素是前列腺癌基于T细胞的免疫疗法中合适的候选药物。

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