Progress on new vaccine strategies against chronic viral infections

被引:98
作者
Berzofsky, JA
Ahlers, JD
Janik, J
Morris, J
Oh, S
Terabe, M
Belyakov, IM
机构
[1] NCI, Mol Immunogenet & Vaccine Res Sect, Vaccine Branch, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
[2] NIAID, Div Aids, NIH, Bethesda, MD 20892 USA
[3] NCI, Clin Trials Team, Metab Branch, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1172/JCI200422674
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Among the most cost-effective strategies for preventing viral infections, vaccines have proven effective primarily against viruses causing acute, self-limited infections. For these it has been sufficient for the vaccine to mimic the natural virus. However, viruses causing chronic infection do not elicit an immune response sufficient to clear the infection and, as a result, vaccines for these viruses must elicit more effective responses - quantitative and qualitative - than does the natural virus. Here we examine the immunologic and virologic basis for vaccines against three such viruses, HIV, hepatitis C virus, and human papillomavirus, and review progress in clinical trials to date. We also explore novel strategies for increasing the immunogenicity and efficacy of vaccines.
引用
收藏
页码:450 / 462
页数:13
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