| Literature DB >> 32958706 |
Devin M Jones1,2, Kaitlin A Read1,2, Kenneth J Oestreich3.
Abstract
CD4+ Th cells are responsible for orchestrating diverse, pathogen-specific immune responses through their differentiation into a number of subsets, including TH1, TH2, TH9, T follicular helper, T follicular regulatory, and regulatory T cells. The differentiation of each subset is guided by distinct regulatory requirements, including those derived from extracellular cytokine signals. IL-2 has emerged as a critical immunomodulatory cytokine that both positively and negatively affects the differentiation of individual Th cell subsets. IL-2 signals are propagated, in part, via activation of STAT5, which functions as a key regulator of CD4+ T cell gene programs. In this review, we discuss current understanding of the mechanisms that allow IL-2-STAT5 signaling to exert divergent effects across CD4+ T cell subsets and highlight specific roles for this pathway in the regulation of individual Th cell differentiation programs.Entities:
Year: 2020 PMID: 32958706 PMCID: PMC7513451 DOI: 10.4049/jimmunol.2000612
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422