Nakashima Masaaki, Nobori Haruaki, Kuroda Takayuki, Shimba Alice, Miyagawa Satoshi, Hayashi Akane, Matsumoto Kazumi, Yoshida Mei, Baba Kaoru, Kato Teruhisa, Fukao Keita
Shionogi & Co., Ltd., 3-1-1, Futaba-cho, Toyonaka-shi, Osaka, 561-0825, Japan.
Shionogi TechnoAdvance Research Co., Ltd., 3-1-1, Futaba-cho, Toyonaka-shi, Osaka, 561-0825 Japan.
Antiviral Res. 2024 Dec;232:106026. doi: 10.1016/j.antiviral.2024.106026. Epub 2024 Oct 29.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease 2019 (COVID-19) remain a major global health challenge, with aerosol transmission being the primary route of spread. The use of antivirals as medical countermeasures to control SARS-CoV-2 transmission and spread is promising but remains to be clarified. The current study established and used an in vivo hamster aerosol transmission model system to evaluate the efficacy of the protease inhibitor ensitrelvir to prevent the spread of SARS-CoV-2. Male Index Syrian hamsters were intranasally infected with SARS-CoV-2, paired with naïve Contact hamsters, and co-housed for 12 h under conditions to allow for only aerosol transmission. The Index hamsters were treated three times with ensitrelvir starting 8 h post infection, or the Contact hamsters were treated once with ensitrelvir 12 h prior to co-housing. Viral infection and transmission were monitored by evaluating nasal lavage fluid, lung tissues, and body and lung weights. Post-infection administration of ensitrelvir to Index hamsters suppressed virus shedding in a dose-dependent manner. Pre-exposure administration of 750 mg/kg ensitrelvir to naïve Contact hamsters also protected against aerosol SARS-CoV-2 infection in a dose-dependent manner. Furthermore, pre-exposure treatment of 750 mg/kg ensitrelvir supressed body weight loss and lung weight increase of aerosol infected hamsters compared to vehicle-treated hamsters. These findings suggest that ensitrelvir may prevent SARS-CoV-2 spread when administered to infected patients and may prevent or limit SARS-CoV-2 infection when prophylactically administered to non-infected individuals. Both approaches may help protect at-risk individuals, such as family members living with SARS-CoV-2-infected patients.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和2019冠状病毒病(COVID-19)仍然是一项重大的全球卫生挑战,气溶胶传播是主要传播途径。使用抗病毒药物作为控制SARS-CoV-2传播和扩散的医学应对措施很有前景,但仍有待阐明。当前的研究建立并使用了一种体内仓鼠气溶胶传播模型系统,以评估蛋白酶抑制剂恩赛特韦预防SARS-CoV-2传播的效果。雄性叙利亚金仓鼠经鼻感染SARS-CoV-2,与未感染的接触仓鼠配对,并在仅允许气溶胶传播的条件下共同饲养12小时。感染后8小时开始,对指示仓鼠用恩赛特韦进行三次治疗,或者在共同饲养前12小时对接触仓鼠用恩赛特韦进行一次治疗。通过评估鼻腔灌洗液、肺组织以及体重和肺重监测病毒感染和传播情况。对指示仓鼠在感染后给予恩赛特韦治疗以剂量依赖的方式抑制了病毒脱落。对未感染的接触仓鼠预先给予750mg/kg恩赛特韦也以剂量依赖的方式预防了气溶胶SARS-CoV-2感染。此外,与用赋形剂处理的仓鼠相比,预先给予750mg/kg恩赛特韦治疗抑制了气溶胶感染仓鼠的体重减轻和肺重增加。这些发现表明,恩赛特韦在给予感染患者时可能预防SARS-CoV-2传播,在预防性给予未感染个体时可能预防或限制SARS-CoV-2感染。这两种方法都可能有助于保护高危个体,例如与感染SARS-CoV-2患者共同生活的家庭成员。