A Proposal to Use Iterative, Small Clinical Trials to Optimize Therapeutic HIV Vaccine Immunogens to Launch Therapeutic HIV Vaccine Development

被引:0
作者
Shapiro, Stuart Z. [1 ]
机构
[1] NIAID, Vaccine Res Program, Div Aids, Bethesda, MD 20892 USA
关键词
T-CELL RESPONSE; INFECTION; DIVERSITY; ESCAPE;
D O I
10.1089/aid.2014.0172
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The HIV cure agenda has rekindled interest in the development of a therapeutic HIV vaccine. An iterative clinical trial strategy that proved successful for the development of effective cancer chemotherapies in the 1960s may be applicable to the development of a CD8 T lymphocyte-based therapeutic HIV vaccine. However, while cancer chemotherapy development could begin with iterative clinical trials to improve the use of active drugs, the first step in therapeutic HIV vaccine design should be discovery of immunogen constructs with potential for activity and their optimization to meet the challenges of HIV-1 sequence diversity and human polymorphism in T cell antigen presentation. A strategy for doing this is discussed in this article. The proposed strategy relies on a major commitment by funding organizations to fund organized and coordinated manufacture and clinical testing of a series of first- and second-generation constructs to test basic concepts in product design. This is presented as an alternative to funding a more traditional competition among private manufacturers and product champions of individual, already designed products.
引用
收藏
页码:49 / 55
页数:7
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