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Th9细胞生成的T细胞受体及共刺激信号

T Cell Receptor and Co-Stimulatory Signals for Th9 Generation.

作者信息

Meylan Françoise, Gomez-Rodriguez Julio

机构信息

Immunoregulation Section, Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, 10 Center Drive, Building 10, Room 13C120, Bethesda, MD, 20892, USA.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 9000 Rockville Pike., Bldg. 49, Room 4C64, Bethesda, MD, 20892, USA.

出版信息

Methods Mol Biol. 2017;1585:59-71. doi: 10.1007/978-1-4939-6877-0_5.

Abstract

In vitro polarization of naïve CD4 T cells toward distinct T helper lineages is crucial for establishing the factors and features that determine the differentiation, stability, and effector function for each T helper subsets. In this regard, the recently defined Th9 subset has been reported with two essential cytokines requirement for their generation. Generating Th9 cells in vitro from naïve CD4 T cells requires the combination of TGF-β and IL-4. However, the amount of IL-9 producing under these minimal conditions is often small. The intent of this chapter is to provide examples to increase the generation of IL-9 producing T cells in vitro by modulating TCR strength and co-stimulation through the TNF family member TL1A. We hope that these methods to efficiently differentiate naïve CD4 T cells toward IL-9 producing cells will facilitate understanding the differentiation and function of Th9 cells and their pathogenesis in various inflammatory and autoimmune diseases.

摘要

将初始CD4 T细胞体外极化为不同的辅助性T细胞谱系,对于确定决定每个辅助性T细胞亚群分化、稳定性和效应器功能的因素及特征至关重要。在这方面,最近定义的Th9亚群已被报道生成时需要两种关键细胞因子。从初始CD4 T细胞体外生成Th9细胞需要转化生长因子-β(TGF-β)和白细胞介素-4(IL-4)的组合。然而,在这些最低条件下产生的白细胞介素-9(IL-9)量通常很少。本章的目的是提供实例,通过调节T细胞受体(TCR)强度和经由肿瘤坏死因子(TNF)家族成员TL1A的共刺激,来增加体外产生IL-9的T细胞的生成。我们希望这些将初始CD4 T细胞有效分化为产生IL-9细胞的方法,将有助于理解Th9细胞的分化和功能及其在各种炎症和自身免疫性疾病中的发病机制。

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