Cutting Edge: Murine Cytomegalovirus Induces a Polyfunctional CD4 T Cell Response
Author(s) -
Ramon Arens,
Peng Wang,
John Sidney,
Andrea Loewendorf,
Alessandro Sette,
Stephen P. Schoenberger,
Bjoern Peters,
Chris A. Benedict
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.10.6472
Subject(s) - cytotoxic t cell , biology , epitope , t cell , immune system , cd8 , cytomegalovirus , immunology , cytokine , spleen , virology , acquired immune system , virus , antigen , herpesviridae , viral disease , in vitro , genetics
CD4 T lymphocytes regulate the adaptive immune response to most viruses, both by providing help to CD8 T cells and B cells as well as through direct antiviral activity. Currently, no mouse cytomegalovirus (MCMV)-specific CD4 T cell responses are known. In this study, we identify and characterize 15 I-A(b)-restricted CD4 T cell responses specific for MCMV epitopes. CD4 T cells accumulate to high levels in the spleen and lungs during acute infection and produce multiple cytokines (IFN-gamma, TNF, IL-2, IL-10, and IL-17). Interestingly, IL-17 and IFN-gamma production within epitope-specific cells was found to be mutually exclusive. CD4 T cells recognizing a peptide derived from m09 were only detectable at later times of infection and displayed a unique cytokine production profile. In total, this study reveals that the MCMV-specific CD4 T cell response is complex and functionally diverse, highlighting its important role in controlling this persistent pathogen.
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