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

机译:使用迭代的小型临床试验来优化治疗性HIV疫苗免疫原以启动治疗性HIV疫苗开发的建议

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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.
机译:HIV治疗议程重新激发了人们对开发治疗性HIV疫苗的兴趣。在1960年代成功开发出有效的癌症化学疗法的迭代临床试验策略可能适用于基于CD8 T淋巴细胞的治疗性HIV疫苗的开发。然而,尽管癌症化学疗法的开发可以从反复的临床试验开始以改善活性药物的使用,但治疗性HIV疫苗设计的第一步应该是发现具有活性潜力的免疫原构建体,并对其进行优化以应对HIV-1序列的挑战T细胞抗原呈递的多样性和人类多态性。本文讨论了执行此操作的策略。提议的策略依赖于资助组织的主要承诺,即资助一系列第一代和第二代结构的组织化,协调性制造和临床测试,以测试产品设计中的基本概念。这是为资助私人制造商与已经设计好的单个产品的产品支持者之间更传统的竞争提供的一种替代方法。

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