Vaccinia virus-specific CD4+ T cell responses target a set of antigens largely distinct from those targeted by CD8+ T cell responses

被引:77
|
作者
Moutaftsi, Magdalini
Bui, Huynh-Hoa
Peters, Bjoern
Sidney, John
Salek-Ardakani, Shahram
Oseroff, Carla
Pasquetto, Valerie
Crotty, Shane
Croft, Michael
Lefkowitz, Elliot J.
Grey, Howard
Sette, Alessandro
机构
[1] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, La Jolla, CA 92037 USA
[2] La Jolla Inst Allergy & Immunol, Div Mol Immunol, La Jolla, CA 92037 USA
[3] Univ Alabama Birmingham, Dept Microbiol, Mol & Genet Bioinformat Facil, Birmingham, AL 35294 USA
来源
JOURNAL OF IMMUNOLOGY | 2007年 / 178卷 / 11期
关键词
D O I
10.4049/jimmunol.178.11.6814
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies have defined vaccinia virus (VACV)-specific CD8(+) T cell epitopes in mice and humans. However, little is known about the epitope specificities of CD4(+) T cell responses. In this study, we identified 14 I-A(b)-restricted VACV-specific CD4+ T cell epitopes by screening a large set of 2146 different 15-mer peptides in C57BL/6 mice. These epitopes account for similar to 20% of the total anti-VACV CD4(+) T cell response and are derived from 13 different viral proteins. Surprisingly, none of the CD4(+) T cell epitopes identified was derived from VACV virulence factors. Although early Ags were recognized, late Ags predominated as CD4(+) T cell targets. These results are in contrast to what was previously found in CD8(+) T cells responses, where early Ags, including virulence factors, were prominently recognized. Taken together, these results highlight fundamental differences in immunodominance of CD4(+) and CD8(+) T cell responses to a complex pathogen.
引用
收藏
页码:6814 / 6820
页数:7
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