A Cell-Intrinsic Requirement for NF-κB-Inducing Kinase in CD4 and CD8 T Cell Memory

被引:38
作者
Rowe, Alexander M. [1 ]
Murray, Susan E. [1 ]
Raue, Hans-Peter [2 ]
Koguchi, Yoshinobu [1 ]
Slifka, Mark K. [1 ,2 ]
Parker, David C. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Beaverton, OR 97006 USA
关键词
SECONDARY LYMPHOID-TISSUE; MHC CLASS-II; DENDRITIC CELLS; VIRAL-INFECTION; NF-KAPPA-B2; PATHWAY; IMMUNE-RESPONSES; SELF-TOLERANCE; IN-VIVO; ACTIVATION; MICE;
D O I
10.4049/jimmunol.1301328
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NF-kappa B-inducing kinase [(NIK), MAP3K14] is an essential kinase linking a subset of TNFR family members to the noncanonical NF-kappa B pathway. To assess the cell-intrinsic role of NIK in murine T cell function, we generated mixed bone marrow chimeras using bone marrow from NIK knockout (KO) and wild-type (WT) donor mice and infected the chimeras with lymphocytic choriomeningitis virus (LCMV). The chimeras possess an apparently normal immune system, including a mixture of NIK KO and WT T cells, and the virus was cleared normally. Comparison of the NIK KO and WT CD4 and CD8 T cell responses at 8 d post infection revealed modest but significant differences in the acute response. In both CD4 and CD8 compartments, relatively fewer activated (CD44(hi)) NIK KO T cells were present, but within the CD44(hi) population, a comparable percentage of the activated cells produced IFN-gamma in response to ex vivo stimulation with antigenic LCMV peptides, although IL-7R expression was reduced in the NIK KO CD8 T cells. Assessment of the LCMV-specific memory at 65 d post infection revealed many more LCMV-specific WT memory T cells than NIK KO memory T cells in both the CD4 and the CD8 compartments, although the small number of surviving NIK KO memory T cells responded to secondary challenge with virus. These results demonstrate a cell-intrinsic requirement for NIK in the generation and/or maintenance of memory T cells in response to acute viral infection.
引用
收藏
页码:3663 / 3672
页数:10
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