CD4+ T cells can protect APC from CTL-mediated elimination

被引:35
|
作者
Mueller, Scott N.
Jones, Claerwen M.
Stock, Angus T.
Suter, Mark
Heath, William R.
Carbone, Francis R. [1 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[2] Univ Zurich, Inst Virol, Zurich, Switzerland
[3] Walter & Eliza Hall Inst Med Res, Immunol Div, Parkville, Vic, Australia
来源
JOURNAL OF IMMUNOLOGY | 2006年 / 176卷 / 12期
关键词
D O I
10.4049/jimmunol.176.12.7379
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Professional APC play a central role in generating antiviral CD8(+) CTL immunity. However, the fate of such APC following interaction with these same CTL remains poorly understood. We have shown previously that prolonged Ag presentation persists in the presence of a strong CTL response following HSV infection. In this study, we examined the mechanism of survival of APC in vivo when presenting an,immunodominant determinant from HSV. We show that transferred peptide-labeled dendritic cells were eliminated from draining lymph nodes in the presence of HSV-specific CTL. Maturation of dendritic cells with LPS or anti-CD40 before injection protected against CTL lysis in vivo. Furthermore, endogenous APC could be eliminated from draining lymph nodes early after HSV infection by adoptive transfer of HSV-specific CTL, yet the cotransfer of significant virus-specific CD4(+) T cell help promoted prolonged Ag presentation. This suggests that Th cells may assist in prolonging class I-restricted Ag presentation, potentially enhancing CTL recruitment and allowing more efficient T cell priming.
引用
收藏
页码:7379 / 7384
页数:6
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