Center for Translational Antiviral Research, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, 30303, USA.
Virology Division, Department of Laboratory Medicine, University of Washington, Seattle, WA, 98185, USA.
Nat Commun. 2022 Jul 29;13(1):4416. doi: 10.1038/s41467-022-32045-1.
SARS-CoV-2 variants of concern (VOC) have triggered infection waves. Oral antivirals such as molnupiravir promise to improve disease management, but efficacy against VOC delta was questioned and potency against omicron is unknown. This study evaluates molnupiravir against VOC in human airway epithelium organoids, ferrets, and a lethal Roborovski dwarf hamster model of severe COVID-19-like lung injury. VOC were equally inhibited by molnupiravir in cells and organoids. Treatment reduced shedding in ferrets and prevented transmission. Pathogenicity in dwarf hamsters was VOC-dependent and highest for delta, gamma, and omicron. All molnupiravir-treated dwarf hamsters survived, showing reduction in lung virus load from one (delta) to four (gamma) orders of magnitude. Treatment effect size varied in individual dwarf hamsters infected with omicron and was significant in males, but not females. The dwarf hamster model recapitulates mixed efficacy of molnupiravir in human trials and alerts that benefit must be reassessed in vivo as VOC evolve.
关注的 SARS-CoV-2 变体 (VOC) 引发了感染浪潮。口服抗病毒药物,如莫努匹韦,有望改善疾病管理,但对 VOC 德尔塔的疗效存在疑问,对奥密克戎的效力尚不清楚。本研究评估了莫努匹韦对人类气道上皮类器官、雪貂和致命的罗伯罗夫斯基仓鼠严重 COVID-19 样肺损伤模型中的 VOC 的作用。在细胞和类器官中,VOC 被莫努匹韦同等抑制。治疗可减少雪貂中的脱落并阻止传播。在仓鼠中的致病性取决于 VOC,德尔塔、伽马和奥密克戎的致病性最高。所有接受莫努匹韦治疗的仓鼠都存活下来,从一个(德尔塔)到四个(伽马)数量级的肺病毒载量减少。感染奥密克戎的个别仓鼠的治疗效果大小不同,在雄性仓鼠中显著,但在雌性仓鼠中不显著。仓鼠模型再现了莫努匹韦在人体试验中的混合疗效,并提醒人们随着 VOC 的演变,必须在体内重新评估其获益。