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

Interleukin (IL)-21 is the most recently recognized of the cytokines that share the common cytokine receptor γ chain (γ(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 bo...

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Detalles Bibliográficos
Autores principales: Zeng, Rong, Spolski, Rosanne, Finkelstein, Steven E., Oh, SangKon, Kovanen, Panu E., Hinrichs, Christian S., Pise-Masison, Cynthia A., Radonovich, Michael F., Brady, John N., Restifo, Nicholas P., Berzofsky, Jay A., Leonard, Warren J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212766/
https://www.ncbi.nlm.nih.gov/pubmed/15630141
http://dx.doi.org/10.1084/jem.20041057
Descripción
Sumario:Interleukin (IL)-21 is the most recently recognized of the cytokines that share the common cytokine receptor γ chain (γ(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-γ 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.