PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
Grimalkin Partners, Silver Spring, Maryland, USA.
Clin Microbiol Rev. 2022 Sep 21;35(3):e0000821. doi: 10.1128/cmr.00008-21. Epub 2022 Jul 6.
The timelines for developing vaccines against infectious diseases are lengthy, and often vaccines that reach the stage of large phase 3 field trials fail to provide the desired level of protective efficacy. The application of controlled human challenge models of infection and disease at the appropriate stages of development could accelerate development of candidate vaccines and, in fact, has done so successfully in some limited cases. Human challenge models could potentially be used to gather critical information on pathogenesis, inform strain selection for vaccines, explore cross-protective immunity, identify immune correlates of protection and mechanisms of protection induced by infection or evoked by candidate vaccines, guide decisions on appropriate trial endpoints, and evaluate vaccine efficacy. We prepared this report to motivate fellow scientists to exploit the potential capacity of controlled human challenge experiments to advance vaccine development. In this review, we considered available challenge models for 17 infectious diseases in the context of the public health importance of each disease, the diversity and pathogenesis of the causative organisms, the vaccine candidates under development, and each model's capacity to evaluate them and identify correlates of protective immunity. Our broad assessment indicated that human challenge models have not yet reached their full potential to support the development of vaccines against infectious diseases. On the basis of our review, however, we believe that describing an ideal challenge model is possible, as is further developing existing and future challenge models.
开发针对传染病的疫苗需要很长时间,而且经常有在大规模 3 期临床试验阶段的疫苗未能提供预期的保护效力。在开发的适当阶段应用感染和疾病的受控人体挑战模型可以加速候选疫苗的开发,实际上在某些有限的情况下已经成功地做到了这一点。人体挑战模型可能有潜力用于收集关于发病机制的关键信息,为疫苗的菌株选择提供信息,探索交叉保护免疫,确定保护的免疫相关性和感染或候选疫苗引起的保护机制,指导关于适当试验终点的决策,并评估疫苗的功效。我们编写这份报告是为了激励科学家们利用受控人体挑战实验的潜力来推进疫苗开发。在这篇综述中,我们根据每种疾病的公共卫生重要性、病原体的多样性和发病机制、正在开发的疫苗候选物以及每种模型评估它们和确定保护免疫相关性的能力,考虑了针对 17 种传染病的现有挑战模型。我们的广泛评估表明,人体挑战模型尚未充分发挥潜力来支持传染病疫苗的开发。然而,根据我们的综述,我们认为描述一个理想的挑战模型是可能的,并且可以进一步开发现有的和未来的挑战模型。