Identification of cryptic MHC I-restricted epitopes encoded by HIV-1 alternative reading frames

被引:71
作者
Cardinaud, S
Moris, A
Février, M
Rohrlich, PS
Weiss, L
Langlade-Demoyen, P
Lemonnier, FA
Schwartz, O
Habel, A
机构
[1] Inst Pasteur, Unite Cellulaire Antivirale, CNRS, Unite Associe Rech 1930, F-75724 Paris 15, France
[2] Hop Europeen Georges Pompidou, Serv Immunol Clin, F-75908 Paris 15, France
关键词
HLA-B7; CTL; transgenic mice; KO mice;
D O I
10.1084/jem.20031869
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human immunodeficiency virus (HIV) 1 major histocompatibility complex (MHC) I-restricted epitopes are widely believed to be derived from viral proteins encoded by primary open reading frames. However, the HIV-1 genome contains alternative reading frames (ARFs) potentially encoding small polypeptides. We have identified a panel of epitopes encoded by ARFs within the gag, pol, and env genes. The corresponding epitopic peptides were immunogenic in mice humanized for MHC-I molecules. In addition, cytotoxic T lymphocytes recognizing these epitopes were found in HIV-infected patients. These results reveal the existence of atypical mechanisms of HIV-1 epitope generation. They indicate that the repertoire of epitopes recognized by the cellular anti-HIV-1 immune response is broader than initially thought. This should be taken Into account when designing vaccine strategies aimed at activating these responses.
引用
收藏
页码:1053 / 1063
页数:11
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