Vaccinia Virus-Specific CD4+ T Cell Responses Target a Set of Antigens Largely Distinct from Those Targeted by CD8+ T Cell Responses
Author(s) -
Magdalini Moutaftsi,
HuynhHoa Bui,
Bjoern Peters,
John Sidney,
Shahram SalekArdakani,
Carla Oseroff,
Valérie Pasquetto,
Shane Crotty,
Michael Croft,
Elliot J. Lefkowitz,
Howard M. Grey,
Alessandro Sette
Publication year - 2007
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.178.11.6814
Subject(s) - epitope , immunodominance , biology , vaccinia , virology , t cell , cd8 , antigen , cytotoxic t cell , virus , virulence , immunology , immune system , genetics , gene , in vitro , recombinant dna
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 approximately 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.
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