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Dynamic Roles for IL-2–STAT5 Signaling in Effector and Regulatory CD4+ T Cell Populations
Author(s) -
Devin M. Jones,
Kaitlin A. Read,
Kenneth J. Oestreich
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2000612
Subject(s) - effector , stat5 , microbiology and biotechnology , biology , signal transduction , regulatory t cell , t cell , computational biology , immunology , il 2 receptor , immune system
CD4 + Th cells are responsible for orchestrating diverse, pathogen-specific immune responses through their differentiation into a number of subsets, including T H 1, T H 2, T H 9, 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.

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