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Cell Rep ; 13(6): 1125-1136, 2015 Nov 10.
Article in English | MEDLINE | ID: mdl-26526997

ABSTRACT

Tissue-resident memory T cells (TRM) reside in barrier tissues and provide local immediate protective immunity. Here, we show that the salivary gland (SG) most-effectively induces CD8(+) and CD4(+) TRM cells against murine cytomegalovirus (MCMV), which persists in and spreads from this organ. TRM generation depended on local antigen for CD4(+), but not CD8(+), TRM cells, highlighting major differences in T cell subset-specific demands for TRM development. CMV-specific CD8(+) T cells fail to control virus replication upon primary infection in the SG due to CMV-induced MHC I downregulation in glandular epithelial cells. Using intraglandular infection, we challenge this notion and demonstrate that memory CD8(+) T cells confer immediate protection against locally introduced MCMV despite active viral immune evasion, owing to early viral tropism to cells that largely withstand MHC I downregulation. Thus, we unravel a yet-unappreciated role for memory CD8(+) T cells in protecting mucosal tissues against CMV infection.


Subject(s)
CD8-Positive T-Lymphocytes/immunology , Herpesviridae Infections/immunology , Salivary Glands/immunology , Animals , CD4-Positive T-Lymphocytes/immunology , Cells, Cultured , Genes, MHC Class I , Immune Evasion , Mice , Mice, Inbred C57BL , Muromegalovirus/physiology , Salivary Glands/cytology , Virus Replication
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