Major contribution of codominant CD8 and CD4 T cell epitopes to the human cytomegalovirus-specific T cell repertoire

被引:24
作者
Nastke, MD
Herrgen, L
Walter, S
Wernet, D
Rammensee, HG
Stevanovic, S
机构
[1] Inst Cell Biol, Dept Immunol, D-72076 Tubingen, Germany
[2] Univ Tubingen, Inst Anasthesiol & Transfus Med, Dept Transfus Med, Tubingen, Germany
关键词
HCMV; immunodominance; antiviral T cells; T cell epitopes; adoptive immunotherapy; peptide-based HCMV vaccine;
D O I
10.1007/s00018-004-4363-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human cytomegalovirus (HCMV) infection or reactivation is a cause of morbidity and mortality in immunocompromised individuals. In immunocompetent individuals, in contrast, HCMV is successfully controlled by specific CD8 and CD4 T cells. Knowledge of CD8 and CD4 T cell epitopes from HCMV and their immunodominant features is crucial for the generation of epitope-specific T cells for adoptive immunotherapy and for the development of a peptide-based HCMV vaccine. Therefore, we investigated the natural frequencies of a large number of CD8 and CD4 T cell epitopes, including 10 novel ones. We determined several epitopes as immunodominant. Surprisingly, no clear hierarchies were found for CD8 T cell epitopes, indicating codominance. These results will be valuable for adoptive transfer strategies and support initiatives towards development of a peptide-based HCMV vaccine.
引用
收藏
页码:77 / 86
页数:10
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