T淋巴细胞识别的肿瘤抗原。

B J Van den Eynde, T Boon
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引用次数: 312

摘要

在过去的五年中,自体细胞溶解T淋巴细胞(CTL)识别的人类肿瘤抗原的知识有了很大的增加。到目前为止,遗传和生化方法已经导致了三种抗原的分子鉴定。这些抗原大部分由肽组成,由HLA分子呈递给T细胞。第一类抗原包括由MAGE、BAGE和GAGE等基因编码的抗原,它们在各种不同组织学来源的肿瘤中表达,但在除睾丸外的正常组织中不表达。第二类是由酪氨酸酶、Melan-A/MART-1、gp100和gp75等仅在黑色素瘤和正常黑色素细胞中表达的基因编码的分化抗原。第三类抗原包括由普遍表达的基因中独特的点突变产生的抗原。在大多数情况下,抗原肽是由基因的突变区域编码的。这些抗原中的许多为特异性癌症免疫治疗的新方案提供了有希望的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor antigens recognized by T lymphocytes.

In the last five years, knowledge of human tumor antigens recognized by autologous cytolytic T lymphocytes (CTL) has increased considerably. So far, genetic and biochemical approaches have led to the molecular identification of three classes of antigens. Most of these antigens consist of peptides that are presented to T cells by HLA molecules. The first class comprises antigens encoded by genes such as MAGE, BAGE, and GAGE, which are expressed in various tumors of different histological origins, but not in normal tissues other than testis. The second class represents differentiation antigens encoded by genes that are only expressed in melanoma and normal melanocytes like tyrosinase, Melan-A/MART-1, gp100 and gp75. The third class includes antigens produced by unique point mutations in genes that are ubiquitously expressed. In most cases, the antigenic peptide is encoded by the mutated region of the gene. A number of these antigens provide promising targets for new protocols of specific cancer immunotherapy.

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