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TCRγδ细胞:免疫系统中的一种特殊T细胞亚群。

TCR gamma delta cells: a specialized T-cell subset in the immune system.

作者信息

Bluestone J A, Khattri R, Sciammas R, Sperling A I

机构信息

University of Chicago, Ben May Institute, Illinois, USA.

出版信息

Annu Rev Cell Dev Biol. 1995;11:307-53. doi: 10.1146/annurev.cb.11.110195.001515.

Abstract

Specificity, memory, and self/nonself discrimination are the essential principles that underlie the acquired immune response. From birth through one's life, the immune system is continually responding to new environmental challenges (e.g. bacteria and viruses) and developing a specific, long-lasting immunity to those challenges. The first exposure to a pathogen results in the recruitment of multiple cell types, including macrophages, dendritic cells, and assorted leukocytes, that initiate an antigen nonspecific inflammatory response designed to attract T cells and B cells to the inflammatory sites including the draining lymph nodes. The foreign antigens are concentrated within the professional antigen-presenting cells (APCs) that process and present small antigenic peptides to CD4+ and CD8+ T cells in association with class II and class I major histocompatibility complex (MHC) molecules, respectively. The activated CD4+ T-cell receptor (TCR) alpha beta cells respond vigorously to the pathogen in an antigen-specific manner, liberating a barrage of cytokines that induce B cells to differentiate to antibody-secreting plasma cells and likewise cause CD8+ cells to differentiate into cytolytic effectors. The T cells and B cells expand in an evolving, highly specific manner to control the initial infection while developing long-term acquired immunity such that any further infection by that pathogen is virtually impossible. Thus TCR alpha beta T cells are the central lymphocyte in the immune system, providing specific pathogen recognition and long-term memory all within the context of distinguishing foreign from self antigens. Yet, during a primary immune response, there is a lag time of approximately 3 to 4 days before antigen-specific responses are evident, and TCR alpha beta responses do not peak until approximately day 7. Therefore, it is essential that other strategies are employed by the immune system in order to mount an aggressive early immune response.

摘要

特异性、记忆性以及自我/非自我识别是获得性免疫反应的基本原理。从出生到生命结束,免疫系统不断应对新的环境挑战(如细菌和病毒),并针对这些挑战形成特异性的、持久的免疫力。首次接触病原体时,会募集多种细胞类型,包括巨噬细胞、树突状细胞和各类白细胞,引发旨在吸引T细胞和B细胞至包括引流淋巴结在内的炎症部位的抗原非特异性炎症反应。外来抗原集中在专职抗原呈递细胞(APC)内,这些细胞分别与II类和I类主要组织相容性复合体(MHC)分子结合,处理并向CD4+和CD8+ T细胞呈递小的抗原肽。活化的CD4+ T细胞受体(TCR)αβ细胞以抗原特异性方式对病原体做出强烈反应,释放大量细胞因子,诱导B细胞分化为分泌抗体的浆细胞,同样使CD8+细胞分化为细胞溶解效应细胞。T细胞和B细胞以不断演变的、高度特异性的方式扩增,以控制初始感染,同时形成长期获得性免疫,使得该病原体再次感染几乎不可能发生。因此,TCRαβ T细胞是免疫系统中的核心淋巴细胞,在区分外来抗原和自身抗原的背景下,提供特异性病原体识别和长期记忆。然而,在初次免疫反应期间,在抗原特异性反应明显之前大约有3至4天的延迟期,TCRαβ反应直到大约第7天才达到峰值。因此,免疫系统必须采用其他策略来发起积极的早期免疫反应。

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