Suppr超能文献

T细胞识别B细胞非霍奇金淋巴瘤独特型蛋白的重链互补决定区3。

T cells recognize the VH complementarity-determining region 3 of the idiotypic protein of B cell non-Hodgkin's lymphoma.

作者信息

Wen Y J, Lim S H

机构信息

Department of Haematology, University of Wales College of Medicine, Cardiff, GB.

出版信息

Eur J Immunol. 1997 Apr;27(4):1043-7. doi: 10.1002/eji.1830270435.

Abstract

The idiotypic protein expressed by B lymphoma cells is a clone-specific tumor antigen which may be suitable for immune targeting by T cells. In this study, we cloned the immunoglobulin heavy chain variable gene (VH) of the idiotypic protein from a patient with B cell lymphoma and used a synthetic peptide of 22 amino acids corresponding to the VH complementarity-determining region (CDR)-3 of the idiotypic protein to investigate whether autologous T cells could recognize this unique peptide. We demonstrated that autologous T cells possessing both CD4+ and CD8+ phenotypes could be propagated. The T cells were able to proliferate, secrete cytokines, and lyse autologous cells presensitized with the specific peptide in a major histocompatibility complex-dependent manner. Moreover, these CDR3 peptide-primed T cells were also able to kill autologous lymphoma cells. Our results therefore offer new perspectives for specific therapeutic vaccination for the treatment of B cell lymphoma.

摘要

B淋巴瘤细胞表达的独特型蛋白是一种克隆特异性肿瘤抗原,可能适合T细胞进行免疫靶向。在本研究中,我们从一名B细胞淋巴瘤患者中克隆了独特型蛋白的免疫球蛋白重链可变基因(VH),并使用与独特型蛋白VH互补决定区(CDR)-3对应的22个氨基酸的合成肽,来研究自体T细胞是否能够识别这种独特的肽。我们证明了同时具有CD4+和CD8+表型的自体T细胞能够增殖。这些T细胞能够增殖、分泌细胞因子,并以主要组织相容性复合体依赖的方式裂解用特异性肽预致敏的自体细胞。此外,这些经CDR3肽致敏的T细胞也能够杀死自体淋巴瘤细胞。因此,我们的结果为B细胞淋巴瘤的特异性治疗性疫苗接种提供了新的视角。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验