Unité de Virologie, Institut de Recherche Biomédicale des Armées, Brétigny-sur-Orge, France
Unité de Virologie, Institut de Recherche Biomédicale des Armées, Brétigny-sur-Orge, France.
Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.01683-19.
Forty years after the last endemic smallpox case, variola virus (VARV) is still considered a major threat to humans due to its possible use as a bioterrorism agent. For many years, the risk of disease reemergence was thought to solely be through deliberate misuse of VARV strains kept in clandestine laboratories. However, recent experiments using synthetic biology have proven the feasibility of recreating a poxvirus , implying that VARV could, in theory, be resurrected. Because of this new perspective, the WHO Advisory Committee on VARV Research released new recommendations concerning research on poxviruses that strongly encourages pursuing the development of new antiviral drugs against orthopoxviruses. In 2018, the U.S. FDA advised in favor of two molecules for smallpox treatment, tecovirimat and brincidofovir. This review highlights the difficulties to develop new drugs targeting an eradicated disease, especially as it requires working under the FDA "animal efficacy rule" with the few, and imperfect, animal models available.
在最后一例地方性天花病例发生 40 年后,由于天花病毒(VARV)有可能被用作生物恐怖主义制剂,因此仍被视为对人类的重大威胁。多年来,人们一直认为疾病再次出现的风险仅源于故意滥用保存在秘密实验室中的 VARV 株。然而,最近使用合成生物学进行的实验证明了重现痘病毒的可行性,这意味着理论上 VARV 可以被复活。由于这种新的观点,世界卫生组织天花病毒咨询委员会发布了有关痘病毒研究的新建议,强烈鼓励开发针对正痘病毒的新型抗病毒药物。2018 年,美国食品和药物管理局(FDA)建议使用两种天花治疗药物,tecovirimat 和 brincidofovir。这篇综述强调了针对已根除疾病开发新药的困难,特别是因为这需要在 FDA 的“动物疗效规则”下进行,而可用的动物模型数量很少且不完美。