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 PMID:15630141  

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

Rong Zeng | Rosanne Spolski | Steven E Finkelstein | SangKon Oh | Panu E Kovanen | Christian S Hinrichs | Cynthia A Pise-Masison | Michael F Radonovich | John N Brady | Nicholas P Restifo | Jay A Berzofsky | Warren J Leonard
The Journal of experimental medicine | 2005

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 (CD44high) and naive (CD44low) 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.

Pubmed ID: 15630141

Research resources used in this publication

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Associated grants

  • Agency: Intramural NIH HHS, United States
    Id: Z01 BC010763-01
  • Agency: Intramural NIH HHS, United States
    Id: Z99 CA999999

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