Human CD4+ CD25high cells suppress proliferative memory lymphocyte responses to herpes simplex virus type 2

被引:22
作者
Diaz, George A.
Koelle, David M.
机构
[1] Univ Washington, Dept Med, Seattle, WA 98195 USA
[2] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pathobiol, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[5] Benaroya Res Inst, Seattle, WA 98101 USA
关键词
REGULATORY T-CELLS; HUMAN-IMMUNODEFICIENCY-VIRUS; IN-VITRO PROLIFERATION; IMMUNE-RESPONSES; ANTIGENS; LESIONS; EXPRESSION; INFECTION; TEGUMENT; GENE;
D O I
10.1128/JVI.00656-06
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Lymphocytes with the regulatory CD4(+) CD25(+) phenotype frequently suppress memory T-cell responses. Murine herpes simplex virus type 1 (HSV-1) models have shown that CD4(+) CD25(+) cells can limit immunity-mediated corneal damage but slow viral clearance. We investigated the effect of CD4(+) CD25(+) cells from healthy HSV-2-infected humans on recall proliferative (CD4) responses to HSV-2. Depletion and reconstitution experiments were consistent with a suppressive effect of autologous blood-derived CD4(+) CD25(+) cells for whole HSV-2 antigen. Regulatory T cells may modulate human CD4 memory responses to HSV-2 and influence their antiviral and inflammatory functions.
引用
收藏
页码:8271 / 8273
页数:3
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