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白细胞介素-17家族细胞因子与效应T细胞谱系不断扩大的多样性。

IL-17 family cytokines and the expanding diversity of effector T cell lineages.

作者信息

Weaver Casey T, Hatton Robin D, Mangan Paul R, Harrington Laurie E

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

Annu Rev Immunol. 2007;25:821-52. doi: 10.1146/annurev.immunol.25.022106.141557.

Abstract

Since its conception two decades ago, the Th1-Th2 paradigm has provided a framework for understanding T cell biology and the interplay of innate and adaptive immunity. Naive T cells differentiate into effector T cells with enhanced functional potential for orchestrating pathogen clearance largely under the guidance of cytokines produced by cells of the innate immune system that have been activated by recognition of those pathogens. This secondary education of post-thymic T cells provides a mechanism for appropriately matching adaptive immunity to frontline cues of the innate immune system. Owing in part to the rapid identification of novel cytokines of the IL-17 and IL-12 families using database searches, the factors that specify differentiation of a new effector T cell lineage-Th17-have now been identified, providing a new arm of adaptive immunity and presenting a unifying model that can explain many heretofore confusing aspects of immune regulation, immune pathogenesis, and host defense.

摘要

自二十年前提出以来,Th1-Th2范式为理解T细胞生物学以及固有免疫和适应性免疫的相互作用提供了一个框架。在很大程度上,初始T细胞在被激活以识别病原体的固有免疫系统细胞产生的细胞因子的指导下,分化为具有更强功能潜力的效应T细胞,以协调病原体清除。胸腺后T细胞的这种二次教育提供了一种机制,使适应性免疫能够与固有免疫系统的一线信号适当匹配。部分由于通过数据库搜索快速鉴定出IL-17和IL-12家族的新型细胞因子,现已确定了指定新的效应T细胞谱系——Th17细胞分化的因素,这提供了适应性免疫的新分支,并提出了一个统一模型,该模型可以解释免疫调节、免疫发病机制和宿主防御中许多迄今为止令人困惑的方面。

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