Leiden University Medical Centre, Leiden, Netherlands.
Leiden University Medical Centre, Leiden, Netherlands.
Lancet Infect Dis. 2018 Oct;18(10):e312-e322. doi: 10.1016/S1473-3099(18)30177-4. Epub 2018 Jun 18.
Controlled human infection (CHI) trials, in which healthy volunteers are experimentally infected, can accelerate the development of novel drugs and vaccines for infectious diseases of global importance. The use of CHI models is expanding from around 60 studies in the 1970s to more than 120 publications in this decade, primarily for influenza, rhinovirus, and malaria. CHI trials have provided landmark data for several registered drugs and vaccines, and have generated unprecedented scientific insights. Because of their invasive nature, CHI studies demand critical ethical review according to established frameworks. CHI-associated serious adverse events are rarely reported. Novel CHI models need standardised safety data from comparable CHI models to facilitate evidence-based risk assessments, as well as funds to produce challenge inoculum according to regulatory requirements. Advances such as the principle of controlled colonisation, the expansion of models to endemic areas, and the use of genetically attenuated strains will further broaden the scope of CHI trials.
人体受控感染(CHI)试验,即对健康志愿者进行实验性感染,可以加速开发具有全球重要意义的传染病的新药和疫苗。CHI 模型的使用范围已从 20 世纪 70 年代的约 60 项研究扩展到本十年的 120 多项出版物,主要用于流感、鼻病毒和疟疾。CHI 试验为几种已注册的药物和疫苗提供了具有里程碑意义的数据,并产生了前所未有的科学见解。由于其具有侵入性,CHI 研究需要根据既定框架进行严格的伦理审查。CHI 相关的严重不良事件很少报告。新型 CHI 模型需要来自可比 CHI 模型的标准化安全数据,以促进基于证据的风险评估,并提供资金根据监管要求生产挑战接种物。受控定植原则、模型扩展到流行地区以及遗传减毒菌株的使用等进展将进一步扩大 CHI 试验的范围。