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Interleukin-27 in T Cell Immunity

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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 16, 期 2, 页码 2851-2863

出版社

MDPI
DOI: 10.3390/ijms16022851

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资金

  1. Japan Society for the Promotion of Science, Ministry of Health, Labor and Welfare
  2. Ministry of Education, Culture, Sports, Science and Technology (MEXT) in part by Global COE Program Chemical Biology of the Diseases by MEXT, Japan
  3. Grants-in-Aid for Scientific Research [25860803, 25461493] Funding Source: KAKEN

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Interleukin (IL)-27, a member of IL-12/IL-23 heterodimeric family of cytokines, has pleiotropic properties that can enhance or limit immune responses. IL-27 acts on various cell types, including T cells, B cells, macrophages, dendritic cells, natural killer (NK) cells and non-hematopoietic cells. Intensive studies have been conducted especially on T cells, revealing that various subsets of T cells respond uniquely to IL-27. IL-27 induces expansion of Th1 cells by activating signal transducer and activator of transcription (STAT) 1-mediated T-bet signaling pathway. On the other hand, IL-27 suppresses immune responses through inhibition of the development of T helper (Th) 17 cells and induction of IL-10 production in a STAT1- and STAT3-dependent manner. IL-27 is a potentially promising cytokine for therapeutic approaches on various human diseases. Here, we provide an overview of the biology of IL-27 related to T cell subsets, its structure, and production mechanism.

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