Identification of immunodominant epitopes derived from the respiratory syncytial virus fusion protein that are recognized by human CD4 T cells

被引:27
作者
van Bleek, GM
Poelen, MC
van der Most, R
Brugghe, HF
Timmermans, HAM
Boog, CJ
Hoogerhout, P
Otten, HG
van Els, CACM
机构
[1] Univ Utrecht, Med Ctr, Dept Hematol, NL-3508 AB Utrecht, Netherlands
[2] Univ Utrecht, Fac Vet Med, Dept Immunol, NL-3508 AB Utrecht, Netherlands
[3] Natl Inst Publ Hlth & Environm, Lab Vaccine Res, NL-3720 BA Bilthoven, Netherlands
关键词
D O I
10.1128/JVI.77.2.980-988.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Memory CD4 T-cell responses against respiratory syncytial virus (RSV) were evaluated in peripheral blood mononuclear cells of healthy blood donors with gamma interferon enzyme-linked immunospot (Elispot) assays. RSV-specific responses were detected in every donor at levels varying between 0.05 and 0.3% of CD4 T cells. For all donors tested, a considerable component of the CD4 T-cell response was directed against the fusion (F) protein of RSV. We characterized a set of 31 immunodominant antigenic peptides targeted by CD4 T cells in the context of the most prevalent HLA class II molecules within the Caucasian population. Most antigenic peptides were HLA-DR restricted, whereas two dominant DQ peptides were also identified. The antigenic peptides identified were located across the entire sequence of the F protein. Several peptides were presented by more than one major histocompatibility complex class II molecule. Furthermore, most donors recognized several F peptides. Detailed knowledge about immunodominant antigenic peptides will facilitate the ability to monitor CD4 T-cell responses in patients and the measurement of correlates of protection in vaccinated subjects.
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收藏
页码:980 / 988
页数:9
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