4.6 Article

Tc17 CD8 T Cells: Functional Plasticity and Subset Diversity

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JOURNAL OF IMMUNOLOGY
卷 183, 期 11, 页码 7161-7168

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0900368

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资金

  1. National Institutes of Health [R01 CA127153, K08 CA096948]
  2. Patrick C. Walsh Fund
  3. National Science Council and Ministry of Education
  4. Chang Gung Memorial Hospital, Taiwan [350821, 350822]
  5. NATIONAL CANCER INSTITUTE [R01CA127153, K08CA096948] Funding Source: NIH RePORTER

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IL-17-secreting CD8 T cells (Tc17) have been described in several settings, but little is known regarding their functional characteristics. While Tc1 cells produced IFN-gamma and efficiently killed targets, Tc17 cells lacked lytic function in vitro. Interestingly, the small numbers of IFN-gamma-positive or IL-17/IFN-gamma-double-positive cells generated under Tc17 conditions also lacked lytic activity and expressed a similar pattern of cell surface proteins to IL-17-producing cells. As is the case for Th17 (CD4) cells, STAT3 is important for Tc17 polarization, both in vitro and in vivo. Adoptive transfer of highly purified, Ag-specific IL-17-secreting Tc17 cells into Ag-bearing hosts resulted in near complete conversion to an IFN-gamma-secreting phenotype and substantial pulmonary pathology, demonstrating functional plasticity. Tc17 also accumulated to a greater extent than did Tc1 cells, suggesting that adoptive transfer of CD8 T cells cultured in Tc17 conditions may have therapeutic potential for diseases in which IFN-gamma-producing cells are desired. The Journal of Immunology, 2009, 183: 7161-7168.

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