T辅助细胞
免疫系统
生物
受体
免疫学
细胞分化
细胞生物学
细胞因子
T细胞
白细胞介素2受体
遗传学
基因
作者
Michelle Schorer,Vijay K. Kuchroo,Nicole Joller
标识
DOI:10.1007/978-981-32-9717-3_6
摘要
CD4+ T cells play a central role in orchestrating the immune response to a variety of pathogens but also regulate autoimmune responses, asthma, allergic responses, as well as tumor immunity. To cover this broad spectrum of responses, naïve CD4+ T cells differentiate into one of several lineages of T helper cells, including Th1, Th2, Th17, and TFH, as defined by their cytokine pattern and function. The fate decision of T helper cell differentiation integrates signals delivered through the T cell receptor, cytokine receptors, and the pattern of co-stimulatory signals received. In this review, we summarize the contribution of co-stimulatory and co-inhibitory receptors to the differentiation and maintenance of T helper cell responses.
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