Sensi M, Parmiani G
Division of Experimental Oncology D, Istituto Nazionale Tumori, Milan, Italy.
Immunol Today. 1995 Dec;16(12):588-95. doi: 10.1016/0167-5699(95)80082-4.
Tumor-infiltrating lymphocytes (TILs), through displaying a T-cell receptor (TCR) repertoire as heterogeneous as that of normal peripheral blood T cells, show overexpression of TCR variable-gene segments that include clonally expanded TCR sequences. Here, Marialuisa Sensi and Giorgio Parmiani analyze the available information on TCR usage by T cells present in the infiltrate of histologically different tumors and suggest that the analysis of TCR sequences represents a powerful new tool to assess the in vivo immune response to growing tumors. Ultimately, this strategy may lead to the identification and manipulation of T-cell populations endowed with antitumor reactivity.
肿瘤浸润淋巴细胞(TILs)通过展示与正常外周血T细胞一样具有异质性的T细胞受体(TCR)库,表现出TCR可变基因片段的过表达,其中包括克隆性扩增的TCR序列。在此,玛丽娅路易莎·森西和乔治·帕尔米尼分析了关于组织学上不同肿瘤浸润中存在的T细胞使用TCR的现有信息,并表明TCR序列分析是评估体内对生长肿瘤的免疫反应的一种强大的新工具。最终,这一策略可能会导致识别和操控具有抗肿瘤反应性的T细胞群体。