Lovelace Respiratory Research Institute, Albuquerque, New Mexico.
Poxvirus Research Group, SIGA Technologies, Inc, Corvallis, Oregon.
J Infect Dis. 2018 Sep 22;218(9):1490-1499. doi: 10.1093/infdis/jiy326.
Tecovirimat (ST-246) is being developed as an antiviral therapeutic for smallpox for use in the event of an accidental or intentional release. The last reported case of smallpox was 1978 but the potential for use of variola virus for biowarfare has renewed interest in smallpox antiviral therapeutics.
Cynomolgus macaques were challenged with a lethal dose of monkeypox virus (MPXV) by aerosol as a model for human smallpox and treated orally with 10 mg/kg tecovirimat once daily starting up to 8 days following challenge. Monkeys were monitored for survival, lesions, and clinical signs of disease. Samples were collected for measurement of viremia by quantitative real-time polymerase chain reaction, and for white blood cell counts.
Survival in animals initiating treatment up to 5 days postchallenge was 100%. In animals treated starting 6, 7, or 8 days following challenge, survival was 67%, 100%, and 50%, respectively. Treatment initiation up to 4 days following challenge reduced severity of clinical manifestations of infection.
Tecovirimat treatment initiated up to 8 days following a lethal aerosol MPXV challenge improves survival and, when initiated earlier than 5 days after challenge, provides protection from clinical effects of disease, supporting the conclusion that it is a promising smallpox antiviral therapeutic candidate.
特考韦瑞(ST-246)正被开发为一种用于天花的抗病毒疗法,以防意外或故意释放。最后一例天花病例发生在 1978 年,但天花病毒用于生物战的可能性使人们重新关注天花抗病毒疗法。
恒河猴通过气溶胶感染致死剂量的猴痘病毒(MPXV)作为人类天花的模型,并在感染后高达 8 天内每天口服 10 毫克/千克特考韦瑞进行治疗。监测猴子的存活、病变和疾病临床症状。采集样本通过定量实时聚合酶链反应测量病毒血症,并测量白细胞计数。
在感染后高达 5 天开始治疗的动物中,存活率为 100%。在感染后 6、7 或 8 天开始治疗的动物中,存活率分别为 67%、100%和 50%。在感染后 4 天内开始治疗可降低感染临床症状的严重程度。
在致死性气溶胶 MPXV 挑战后高达 8 天开始的特考韦瑞治疗可提高存活率,并且在挑战后 5 天内开始治疗可提供对疾病临床影响的保护,支持其作为一种有前途的天花抗病毒治疗候选药物的结论。