Mechanisms of HIV Protein Degradation into Epitopes: Implications for Vaccine Design

被引:7
作者
Rucevic, Marijana
Boucau, Julie
Dinter, Jens
Kourjian, Georgio
Le Gall, Sylvie [1 ]
机构
[1] Massachusetts Gen Hosp, Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USA
来源
VIRUSES-BASEL | 2014年 / 6卷 / 08期
关键词
HIV; antigen processing; protein degradation; proteasome; aminopeptidase; peptidase; immunogen; vaccine vector; dendritic cells; T cells; viral evolution; MHC CLASS-I; T-CELL RESPONSES; IMMUNODEFICIENCY-VIRUS TYPE-1; HUMAN DENDRITIC CELLS; MODULATES PROTEASOME ACTIVITY; CROSS-PRESENTATION PATHWAY; HIGHLY PATHOGENIC SIV; 20 S PROTEASOMES; ANTIGEN PRESENTATION; ENDOPLASMIC-RETICULUM;
D O I
10.3390/v6083271
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The degradation of HIV-derived proteins into epitopes displayed by MHC-I or MHC-II are the first events leading to the priming of HIV-specific immune responses and to the recognition of infected cells. Despite a wealth of information about peptidases involved in protein degradation, our knowledge of epitope presentation during HIV infection remains limited. Here we review current data on HIV protein degradation linking epitope production and immunodominance, viral evolution and impaired epitope presentation. We propose that an in-depth understanding of HIV antigen processing and presentation in relevant primary cells could be exploited to identify signatures leading to efficient or inefficient epitope presentation in HIV proteomes, and to improve the design of immunogens eliciting immune responses efficiently recognizing all infected cells.
引用
收藏
页码:3271 / 3292
页数:22
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