期刊
EUROPEAN JOURNAL OF IMMUNOLOGY
卷 36, 期 11, 页码 3060-3070出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/eji.200636173
关键词
CD8 T cell; DC; Listeria monocytogenes; mice; tyrosine kinase 2
类别
Tyrosine kinase 2 (Tyk2) contributes to the signals triggered by IL-12 for IFN-gamma production by NK cells and T cells. We found in this study that Tyk2-deficient (-/-) mice showed increased susceptibility at the early stage after an i.p. infection with Listeria monocytogenes, accompanied by impaired IFN-gamma production. The numbers of both MHC class Ib (H2-M3)- or MHC class Ia (K-b)-restricted CD8(+) T cells producing IFN-gamma and exhibiting cytotoxicity were significantly decreased in Tyk2(-/-) mice after infection with L. monocytogenes. Using an adoptive transfer system of OT-I cells expressing OVA(257-264)/K-b-specific TCR into Tyk2(-/-) mice followed by challenge with recombinant L. monocytogenes expressing OVA, we found that the defective Tyk2 signaling in the host environment was at least partially responsible for the impaired CD8(+) T cytotoxic-1 (Tc1) cell responses in Tyk2(-/-) mice following the infection. Adoptive transfer with MHC class 1b- or MHC class Ia-binding peptide-pulsed BM-derived DC from Tyk2(-/-) mice induced lower levels of the Ag-specific CD8(+) Tcl cells producing IFN-y. These results suggest that Tyk2 signaling is also important for DC function in the induction of MHC class Ia- and class Ib-restricted CD8(+) Tc1 cells following L. monocytogenes infection.
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