Polyomavirus-infected dendritic cells induce antiviral CD8+ T lymphocytes

被引:31
作者
Drake, DR
Moser, JM
Hadley, A
Altman, JD
Maliszewski, C
Butz, E
Lukacher, AE
机构
[1] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[4] Immunex Res & Dev Corp, Seattle, WA 98101 USA
关键词
D O I
10.1128/JVI.74.9.4093-4101.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CD8(+) T cells are critical for the clearance of acute polyomavirus infection and the prevention of polyomavirus-induced tumors, but the antigen-presenting cell(s) involved in generating polyomavirus-specific CD8(+) T cells have not been defined. We investigated whether dendritic cells and macrophages are permissive for polyomavirus infection and examined their potential for inducing antiviral CD8(+) T cells. Although dendritic cells and macrophages both supported productive polyomavirus infection, dendritic cells were markedly more efficient at presenting the immunodominant viral epitope to CD8(+) T cells. Additionally, infected dendritic cells, but not infected macrophages, primed anti-polyomavirus CD8(+) T cells in vivo. Treatment with Flt3 ligand, a hematopoietic growth factor that dramatically expands the number of dendritic cells, markedly enhanced the magnitude of virus-specific CD8(+) T-cell responses during acute infection and the pool of memory anti-polyomavirus CD8(+) T cells, These findings suggest that virus-infected dendritic cells induce polyomavirus-specific CD8(+) T cells in vivo and raise the potential for their use as cellular adjuvants to promote CD8(+) T cell surveillance against polyomavirus-induced tumors.
引用
收藏
页码:4093 / 4101
页数:9
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