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不同分化阶段的 CD4 T 细胞谱系塑造了对急性感染的 CD8 T 细胞反应。

Developmentally distinct CD4 T lineages shape the CD8 T cell response to acute infection.

机构信息

Division of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, CA 92037.

Division of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, CA 92037.

出版信息

Proc Natl Acad Sci U S A. 2022 Mar 8;119(10):e2113329119. doi: 10.1073/pnas.2113329119. Epub 2022 Mar 3.

Abstract

SignificanceThe CD4 T response following acute infection is heterogeneous and deploys two distinct modes of suppression coinciding with initial pathogen exposure and resolution of infection. This bimodal suppression of CD8 T cells during priming and contraction is mediated by separate T lineages. These findings make a significant contribution to our understanding of the functional plasticity inherent within T, which allows these cells to serve as a sensitive and dynamic cellular rheostat for the immune system to prevent autoimmune pathology in the face of inflammation attendant to acute infection, enable expansion of the pathogen-specific response needed to control the infection, and reestablish immune homeostasis after the threat has been contained.

摘要

意义

急性感染后 CD4 T 反应具有异质性,并采用两种不同的抑制模式,与初始病原体暴露和感染消退同时发生。这种在启动和收缩过程中对 CD8 T 细胞的双峰抑制是由不同的 T 细胞谱系介导的。这些发现为我们理解 T 细胞内在的功能可塑性做出了重要贡献,这使得这些细胞能够作为免疫系统的敏感和动态细胞变阻器,在急性感染伴随的炎症面前防止自身免疫病理学,使病原体特异性反应得以扩张以控制感染,并在威胁得到控制后重新建立免疫稳态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a59/8915796/355c46b1b9f8/pnas.2113329119fig01.jpg

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