Organ-specific regulation of the CD8 T cell response to Listeria monocytogenes infection

被引:329
作者
Pope, C
Kim, SK
Marzo, A
Williams, K
Jiang, J
Shen, H
Lefrançois, L
机构
[1] Univ Connecticut, Ctr Hlth, Dept Med, Div Rheumat Dis, Farmington, CT 06030 USA
[2] Univ Penn, Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
D O I
10.4049/jimmunol.166.5.3402
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The intestinal mucosal CD8 T cell response to infection with Listeria monocytogenes tvas measured using MHC class I tetramers and was compared with the response in peripheral blood, secondary lymphoid tissue, and liver. To assess the vaccination potential of Listeria and to analyze responses in C57BL/6 mouse strains, a recombinant Listeria expressing OVA (rLM-ova) was generated. The response peaked at 9 days postinfection with a much larger fraction of the intestinal mucosa and liver CD8 T fell pool OVA specific, as compared with the spleen. However, these differences were not linked to bacterial titers in each site. The higher responses in lamina propria and liver resulted in a larger CD8 memory population in these tissues. Furthermore, the level of memory induced mas dependent on infectious dose and inversely correlated with the magnitude of the recall response after oral challenge, Recall responses in the tissues were most robust in the lamina propria and liver, and reactivated Ag-specific T cells produced IFN-gamma, Infection of CD40- or MHC class II-deficient mice induced poor CD8 T cell responses in the intestinal mucosa, but only partially reduced responses in the spleen and liver. Overall, the results point to novel pathways of tissue specific regulation of primary and memory antimicrobial CD8 T cell responses.
引用
收藏
页码:3402 / 3409
页数:8
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