FOXP3型
效应器
细胞生物学
免疫学
Cd4 t细胞
白细胞介素21
调节性T细胞
体外
Treg细胞
T细胞
生物
平衡
白细胞介素2受体
免疫系统
遗传学
作者
Francesco Siracusa,Franziska Muscate,Laura García Pérez
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 65-75
被引量:2
标识
DOI:10.1007/978-1-0716-1311-5_5
摘要
CD4+ T helper (TH) cells are key mediators of immunity, and according to their effector functions, they can be divided into different subsets, namely, TH1, TH2, TH17, and TH22. In order to maintain systemic homeostasis and peripheral tolerance, CD4+ TH cells are counterbalanced by CD4+ T cells with regulatory properties, namely, Foxp3+ regulatory T cells (Foxp3+TREG) and TR1 cells. Here, we describe how to in vitro differentiate murine naïve CD4+ T cells toward helper (TH1, TH2, TH17, and TH22) and regulatory (Foxp3+TREG and TR1) cells.
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