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γδ T细胞的识别模式。

The recognition pattern of gammadelta T cells.

作者信息

Cao Wei, He Wei

机构信息

Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, 5 Dong Dan San Tiao, Beijing 100005, China.

出版信息

Front Biosci. 2005 Sep 1;10:2676-700. doi: 10.2741/1729.

Abstract

The main function of immune system is to recognize and respond to foreign antigens. During the course of evolution, the body has successfully developed four kinds of mechanisms to recognize antigens, including pattern recognition mediated by macrophages, missing-self and induced-self recognition for NK cells, antigen specific recognition for alphabeta T cells and B cells and "broad-spectrum specific" recognition for gammadelta T cells. The three formers have made great progress these years. However, details of antigen recognition by gammadelta T cells are still mysterious. Gammadelta T cells, a class of T cells only existing in primates, differ from alphabeta T cells in TCR diversity, the structure of TCR-CD3 complex, the tissue distribution, the antigens that they recognize and the way involved in recognition. Here, we shed light on the recognition mechanism of gammadelta T cells against several known antigens and discuss the possible response pattern along the research historical process. We put forward a recognition hypothesis for gammadelta TCR that is conformational recognition based on germline encoded recognition. The key germline encoded amino acids dominate the "putative binding box" and are responsible for recognition. Meanwhile, after gammadelta T cells are activated, several other molecules such as CD69, CD16, 2B4, NKG2D also participate in inducing cytotoxicity of activated gammadelta T cells. Obviously, the illustration of recognition mechanism for gammadelta T cells will help to comprehensively understand the whole immune system and design the higher effective multi-epitope vaccines for tumor and infection immunity.

摘要

免疫系统的主要功能是识别外来抗原并作出反应。在进化过程中,机体成功地发展出四种识别抗原的机制,包括巨噬细胞介导的模式识别、自然杀伤细胞(NK细胞)的“缺失自我”和“诱导自我”识别、αβT细胞和B细胞的抗原特异性识别以及γδT细胞的“广谱特异性”识别。前三种机制近年来取得了很大进展。然而,γδT细胞识别抗原的细节仍然神秘。γδT细胞是一类仅存在于灵长类动物中的T细胞,在T细胞受体(TCR)多样性、TCR-CD3复合物结构、组织分布、识别的抗原以及识别所涉及的方式等方面与αβT细胞不同。在此,我们阐明了γδT细胞对几种已知抗原的识别机制,并沿着研究历史进程讨论了可能的反应模式。我们提出了一种针对γδTCR的识别假说,即基于种系编码识别的构象识别。关键的种系编码氨基酸主导“假定结合框”并负责识别。同时,γδT细胞被激活后,其他几种分子如CD69、CD16、2B4、NKG2D也参与诱导活化的γδT细胞的细胞毒性。显然,阐明γδT细胞的识别机制将有助于全面理解整个免疫系统,并设计出针对肿瘤和感染免疫的更高效的多表位疫苗。

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