Affiliation:
1. Division of Basic and Clinical Immunology, University of California, Irvine, California
Abstract
ABSTRACT
The immune responses of naive and different memory subsets of CD4
+
and CD8
+
T cells to human herpesvirus 6 (HHV-6) have not been previously investigated. We show that HHV-6A induces cell division, as measured by 5,6-carboxyfluorescein succinimidyl ester dye and flow cytometry, predominantly in two populations of effector memory CD4
+
and CD8
+
T cells (T
EM
and T
EMRA
); naïve (T
N
) and central memory (T
CM
) CD4
+
and CD8
+
T cells showed almost no cell division. In contrast, HHV-6A induced apoptosis primarily in T
N
and T
CM
CD4
+
and CD8
+
T cells, whereas T
EM
and T
EMRA
CD4
+
and CD8
+
T cells were resistant to HHV-6A-induced apoptosis. HHV-6A-induced apoptosis was associated with activation of caspase-8, caspase-9, and caspase-3, suggesting the involvement of death receptor and mitochondrial signaling pathways. In addition, HHV-6A induced secretion of interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), IL-8, and gamma interferon by peripheral blood mononuclear cells; TNF-α secretion was observed exclusively from CCR7
+
(T
N
plus T
CM
) CD4
+
T cells. These data show that HHV-6 differentially influences the functions of naïve T cells and different subsets of memory CD4
+
and CD8
+
T cells, which in part may be due to differential susceptibility to HHV-6A-induced apoptosis.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
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