4.7 Article

Synergy of IL-21 and IL-15 in regulating CD8+ T cell expansion and function

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JOURNAL OF EXPERIMENTAL MEDICINE
卷 201, 期 1, 页码 139-148

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ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20041057

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  1. Intramural NIH HHS [Z99 CA999999, Z01 BC010763-01] Funding Source: Medline

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Interleukin (IL)-21 is the most recently recognized of the cytokines that share the common cytokine receptor gamma chain (gamma(c)), which is mutated in humans with X-linked severe combined immunodeficiency. We now report that IL-21 synergistically acts with IL-15 to potently promote the proliferation of both memory (CD44(high)) and naive (CD44(low)) phenotype CD8(+) T cells and augment interferon-gamma production in vitro. IL-21 also cooperated, albeit more weakly, with IL-7, but not with IL-2. Correspondingly, the expansion and cytotoxicity of CD8(+) T cells were impaired in IL-21R(-/-) mice. Moreover, in vivo administration of IL-21 in combination with IL-15 boosted antigen-specific CD8(+) T cell numbers and resulted in a cooperative effect on tumor regression, with apparent cures of large, established B16 melanomas. Thus, our studies reveal that IL-21 potently regulates CD8(+) T cell expansion and effector function, primarily in a synergistic context with IL-15.

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