Viral peptide immunogens: current challenges and opportunities

被引:18
作者
Azizi, Ali [2 ,3 ]
Diaz-Mitoma, Francisco [1 ,2 ,3 ]
机构
[1] Childrens Hosp Eastern Ontario, Res Inst, Vaccine Res Ctr, Ottawa, ON K1H 8L1, Canada
[2] Variat Biotechnol Inc, Gatineau, PQ J8T 8R1, Canada
[3] Univ Ottawa, Dept Pathol & Lab Med, Ottawa, ON K1H 8M2, Canada
关键词
vaccine; immune response; viral infection; peptide epitopes;
D O I
10.1002/psc.896
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
Synthetic peptide vaccines have potential to control viral infections. Successful experimental models using this approach include the protection of mice against the lethal Sendai vir-us infection by MHC class I binding CTL peptide epitope. The main benefit of vaccination with peptide epitopes is the ability to minimize the amount and complexity of a well-defined antigen. An appropriate peptide immunogen would also decrease the chance of stimulating a response against self-antigens, thereby providing a safer vaccine by avoiding autoimmunity. In general, the peptide vaccine strategy needs to dissect the specificity of antigen processing, the presence of B-and T-cell epitopes and the MHC restriction of the T-cell responses. This article briefly reviews the implications in the design of peptide vaccines and discusses the various approaches that are applied to improve their immunogenicity. Copyright (c) 2007 European Peptide Society and John Wiley & Sons, Ltd.
引用
收藏
页码:776 / 786
页数:11
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