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Thymic Selection Determines [gamma][delta] T Cell Effector Fate: Antigen-Naive Cells Make Interleukin-17 and Antigen-Experienced Cells Make Interferon [gamma]

by: Kirk D Jensen, Xiaoqin Su, Sunny Shin, Luke Li, Sawsan Youssef, Sho Yamasaki, Lawrence Steinman, Takashi Saito, Richard M Locksley, Mark M Davis, Nicole Baumgarth, Yueh-Hsiu Chien
Immunity, Vol. 29, No. 1. (18 July 2008), pp. 90-100.


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Summary [gamma][delta] T cells uniquely contribute to host immune defense, but how this is accomplished remains unclear. Here, we analyzed the nonclassical major histocompatibility complex class I T10 and T22-specific [gamma][delta] T cells in mice and found that encountering antigen in the thymus was neither required nor inhibitory for their development. But when triggered through the T cell receptor, ligand-naive lymphoid-[gamma][delta] T cells produced IL-17, whereas ligand-experienced cells made IFN-[gamma]. Immediately after immunization, a large fraction of IL-17+ [gamma][delta] T cells were found in the draining lymph nodes days before the appearance of antigen-specific IL-17+ [alpha][beta] T cells. Thus, thymic selection determines the effector fate of [gamma][delta] T cells rather than constrains their antigen specificities. The swift IL-17 response mounted by antigen-naive [gamma][delta] T cells suggests a critical role for these cells at the onset of an acute inflammatory response to novel antigens.


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