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Dynamic Roles for IL-2-STAT5 Signaling in Effector and Regulatory CD4+d T Cell Populations

Journal

JOURNAL OF IMMUNOLOGY
Volume 205, Issue 7, Pages 1721-1730

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.2000612

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Funding

  1. National Institutes of Health [AI134972]

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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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