Recognition of shared melanoma antigens by human tumor-infiltrating lymphocytes.

S L Topalian, S S Hom, Y Kawakami, M Mancini, D J Schwartzentruber, R Zakut, S A Rosenberg
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引用次数: 23

Abstract

We have established that melanomas express shared tumor antigens (Ags) that can be recognized by T cells if presented in the context of self-MHC molecules. Tumor-infiltrating lymphocytes (TILs) from six melanoma patients were tested for lysis of large panels of HLA-matched or unmatched targets representing a variety of tissue types. Lysis was specific for allogeneic melanomas sharing at least one HLA-A, -B, or -C Ag with TILs, and demonstrated commonly expressed tumor Ags. Similar findings were obtained when cytokine secretion by TILs was used to indicate specific Ag recognition. Transfection of the HLA-A2.1 gene into HLA-A2- melanoma lines conferred susceptibility to lysis by HLA-A2 restricted melanoma TILs, demonstrating expression of common tumor Ags among patients of diverse HLA types. These findings have important implications for developing broadly applicable cancer immunotherapies such as vaccines.

人类肿瘤浸润淋巴细胞对黑色素瘤共有抗原的识别。
我们已经确定,黑色素瘤表达共同的肿瘤抗原(Ags),如果在自身mhc分子的背景下呈现,可以被T细胞识别。我们对来自6名黑色素瘤患者的肿瘤浸润淋巴细胞(til)进行了检测,以溶解大量hla匹配或不匹配的靶细胞,这些靶细胞代表了各种组织类型。裂解对同种异体黑素瘤具有特异性,它与TILs至少共享一种HLA-A、-B或-C Ag,并显示出常见的肿瘤Ags。当使用TILs分泌的细胞因子来指示特异性Ag识别时,也得到了类似的结果。将HLA- a2.1基因转染到HLA- a2 -黑色素瘤细胞系中,使其易被HLA- a2限制性黑色素瘤TILs溶解,表明不同HLA类型患者中常见肿瘤Ags的表达。这些发现对开发广泛适用的癌症免疫疗法(如疫苗)具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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