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CD8 T细胞对传染性病原体的反应。

CD8 T cell responses to infectious pathogens.

作者信息

Wong Phillip, Pamer Eric G

机构信息

Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.

出版信息

Annu Rev Immunol. 2003;21:29-70. doi: 10.1146/annurev.immunol.21.120601.141114. Epub 2001 Dec 19.

Abstract

CD8 T cells respond to viral infections but also participate in defense against bacterial and protozoal infections. In the last few years, as new methods to accurately quantify and characterize pathogen-specific CD8 T cells have become available, our understanding of in vivo T cell responses has increased dramatically. Pathogen-specific T cells, once thought to be quite rare following infection, are now known to be present at very high frequencies, particularly in peripheral, nonlymphoid tissues. With the ability to visualize in vivo CD8 T cell responses has come the recognition that T cell expansion is programmed and, to a great extent, independent of antigen concentrations. Comparison of CD8 T cell responses to different pathogens also highlights the intricate relationship between microbially induced innate inflammatory responses and the kinetics, magnitude, and character of long-term T cell responses. This review describes recent progress in some of the major murine models of CD8 T cell-mediated immunity to viral, bacterial, and protozoal infection.

摘要

CD8 T细胞对病毒感染作出反应,同时也参与抵御细菌和原生动物感染。在过去几年中,随着准确量化和表征病原体特异性CD8 T细胞的新方法问世,我们对体内T细胞反应的理解有了显著提高。病原体特异性T细胞,曾被认为在感染后相当罕见,现在已知以非常高的频率存在,特别是在外周非淋巴组织中。随着能够在体内可视化CD8 T细胞反应,人们认识到T细胞扩增是被编程的,并且在很大程度上独立于抗原浓度。对不同病原体的CD8 T细胞反应进行比较,也凸显了微生物诱导的先天性炎症反应与长期T细胞反应的动力学、强度和特征之间的复杂关系。本综述描述了在CD8 T细胞介导的针对病毒、细菌和原生动物感染的免疫的一些主要小鼠模型中的最新进展。

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