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肿瘤浸润淋巴细胞中T细胞抗原受体库有限及抗TCR抗体对小鼠黑色素瘤实验性肺转移的抑制作用

Limited T cell antigen receptor repertoire in tumor-infiltrating lymphocyte and inhibition of experimental lung metastasis of murine melanoma by anti-TCR antibody.

作者信息

Wang R, Taniguchi M

机构信息

Division of Molecular Immunology, Chiba University, Japan.

出版信息

J Immunol. 1995 Feb 15;154(4):1797-803.

PMID:7836764
Abstract

We analyzed the variability of T cell Ag receptor in tumor-infiltrating lymphocytes in primary and metastatic melanomas. Using a very sensitive inverse/double step PCR, we found the preferential V alpha usage of TCR in tumor-infiltrating lymphocytes in which some TCR sequences were homogenous. However, the profile of TCR V alpha expression was different in primary and metastatic melanomas. V alpha 8+, V alpha 2+, V alpha 4+, and V alpha 3+ TCR were the most dominant repertoires in primary melanoma, whereas V alpha 3+ and V alpha 4+ TCR dominated metastatic melanoma. Depletion of V alpha 3 T cells by the injection of tumor-bearing mice with anti-V alpha 3 Ab resulted in protection against experimental lung metastasis, indicating that V alpha 3+ regulatory T cells exist in the tumor site and help metastatic tumor growth.

摘要

我们分析了原发性和转移性黑色素瘤中肿瘤浸润淋巴细胞的T细胞抗原受体的变异性。使用非常灵敏的反向/两步PCR,我们发现在肿瘤浸润淋巴细胞中TCR优先使用Vα,其中一些TCR序列是同质的。然而,原发性和转移性黑色素瘤中TCR Vα表达谱是不同的。Vα8+、Vα2+、Vα4+和Vα3+ TCR是原发性黑色素瘤中最主要的谱系,而Vα3+和Vα4+ TCR在转移性黑色素瘤中占主导。给荷瘤小鼠注射抗Vα3抗体以清除Vα3 T细胞,可预防实验性肺转移,这表明肿瘤部位存在Vα3+调节性T细胞并促进转移性肿瘤生长。

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