Paul-Ehrlich-Institut (PEI), Langen, Germany; Institute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Sciensano, Brussels, Belgium.
Biologicals. 2020 Jul;66:53-61. doi: 10.1016/j.biologicals.2020.04.005. Epub 2020 May 4.
Controlled human infection models can be helpful to study pathogenesis and immune responses as a basis for the development of vaccines. In controlled human infection models, human challenge agents are used to infect healthy volunteers, therefore, ethical considerations include that the exposure studies need to be safe and results should be meaningful, e.g. contribute to a better cure. Both in the US and in Europe, the level of Good Manufacturing Practice required is related to the phase of the study ('sliding scale Good Manufacturing Practice'), and, hence, is much more open to speedy drug development than anticipated. Recommendations included: the development of guidelines for human challenge agents; a focus on strain selection, in particular with regard to strain infectivity, stability and purity; the use of whole genome sequencing; a reference repository of challenge agents, the need for early exchange with regulators to ensure acceptability of strain selection and manufacturing for later drug development; sharing of models and challenge agents.
人体感染控制模型有助于研究发病机制和免疫反应,为疫苗开发提供基础。在人体感染控制模型中,使用感染性人类挑战剂来感染健康志愿者,因此,伦理考虑因素包括暴露研究需要安全,并且结果应该有意义,例如有助于更好地治疗。在美国和欧洲,所需的良好生产规范水平与研究阶段相关(“滑动比例良好生产规范”),因此,比预期更有利于快速药物开发。建议包括:制定人体挑战剂指南;关注菌株选择,特别是菌株感染性、稳定性和纯度;使用全基因组测序;建立挑战剂参考库,需要及早与监管机构交流,以确保后续药物开发中对菌株选择和制造的可接受性;共享模型和挑战剂。