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基于极化细胞因子抑制的 Th2 分化模型。

A model of Th2 differentiation based on polarizing cytokine repression.

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Trends Immunol. 2023 Jun;44(6):399-407. doi: 10.1016/j.it.2023.04.004. Epub 2023 Apr 24.

Abstract

Conventional dendritic cells (cDCs) can integrate multiple stimuli from the environment and provide three separate outputs in terms of antigen presentation, costimulation, and cytokine production; this guides the activation, expansion, and differentiation of distinct functional T helper subsets. Accordingly, the current dogma posits that T helper cell specification requires these three signals in sequence. Data show that T helper 2 (Th2) cell differentiation requires antigen presentation and costimulation from cDCs but does not require polarizing cytokines. In this opinion article, we propose that the 'third signal' driving Th2 cell responses is, in fact, the absence of polarizing cytokines; indeed, the secretion of the latter is actively suppressed in cDCs, concomitant with acquired pro-Th2 functions.

摘要

传统树突状细胞 (cDC) 可以整合来自环境的多种刺激,并在抗原呈递、共刺激和细胞因子产生方面提供三种独立的输出;这指导了不同功能 T 辅助亚群的激活、扩增和分化。因此,目前的共识认为 T 辅助细胞的特化需要这三个信号按顺序出现。有数据表明,T 辅助 2(Th2)细胞的分化需要 cDC 提供抗原呈递和共刺激,但不需要极化细胞因子。在这篇观点文章中,我们提出驱动 Th2 细胞反应的“第三信号”实际上是缺乏极化细胞因子;事实上,后者的分泌在 cDC 中被积极抑制,同时获得了促 Th2 功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a73c/10219849/64a0cf05cf30/nihms-1890042-f0001.jpg

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