Epitope-Specific Regulatory CD4 T Cells Reduce Virus-Induced Illness while Preserving CD8 T-Cell Effector Function at the Site of Infection

被引:21
作者
Liu, Jie [1 ]
Ruckwardt, Tracy J. [1 ]
Chen, Man [1 ]
Nicewonger, John D. [1 ]
Johnson, Teresa R. [1 ]
Graham, Barney S. [1 ]
机构
[1] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
关键词
RESPIRATORY SYNCYTIAL VIRUS; TRANSCRIPTION FACTOR FOXP3; VIRAL-INFECTION; IMMUNODOMINANCE DISPARITIES; MICE; RESPONSES; DISEASE; SUBSETS; ANTIGEN; MODEL;
D O I
10.1128/JVI.00963-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The role of epitope-specific regulatory CD4 T cells in modulating CD8 T-cell-mediated immunopathology during acute viral infection has not been well defined. In the murine model of respiratory syncytial virus (RSV) infection, CD8 T cells play an important role in both viral clearance and immunopathology. We have previously characterized two RSV epitope-specific CD4 T-cell responses with distinct phenotypic properties. One of them, the IA(b)M(209)-specific subset, constitutively expresses FoxP3 and modulates CD8 T-cell function in vitro. We show here that the IA(b)M(209)-specific CD4 T-cell response regulates CD8 T-cell function in vivo and is associated with diminished RSV-induced illness without affecting viral clearance at the site of infection. Achieving the optimal balance of regulatory and effector T-cell function is an important consideration for designing future vaccines.
引用
收藏
页码:10501 / 10509
页数:9
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