Geisbert Thomas W, Mire Chad E, Geisbert Joan B, Chan Yee-Peng, Agans Krystle N, Feldmann Friederike, Fenton Karla A, Zhu Zhongyu, Dimitrov Dimiter S, Scott Dana P, Bossart Katharine N, Feldmann Heinz, Broder Christopher C
Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77550, USA. Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77550, USA.
Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Sci Transl Med. 2014 Jun 25;6(242):242ra82. doi: 10.1126/scitranslmed.3008929.
Nipah virus (NiV) is an emerging zoonotic paramyxovirus that causes severe and often fatal disease in pigs and humans. There are currently no vaccines or treatments approved for human use. Studies in small-animal models of NiV infection suggest that antibody therapy may be a promising treatment. However, most studies have assessed treatment at times shortly after virus exposure before animals show signs of disease. We assessed the efficacy of a fully human monoclonal antibody, m102.4, at several time points after virus exposure including at the onset of clinical illness in a uniformly lethal nonhuman primate model of NiV disease. Sixteen African green monkeys (AGMs) were challenged intratracheally with a lethal dose of NiV, and 12 animals were infused twice with m102.4 (15 mg/kg) beginning at either 1, 3, or 5 days after virus challenge and again about 2 days later. The presence of viral RNA, infectious virus, and/or NiV-specific immune responses demonstrated that all subjects were infected after challenge. All 12 AGMs that received m102.4 survived infection, whereas the untreated control subjects succumbed to disease between days 8 and 10 after infection. AGMs in the day 5 treatment group exhibited clinical signs of disease, but all animals recovered by day 16. These results represent the successful therapeutic in vivo efficacy by an investigational drug against NiV in a nonhuman primate and highlight the potential impact that a monoclonal antibody can have on a highly pathogenic zoonotic human disease.
尼帕病毒(NiV)是一种新出现的人畜共患副粘病毒,可在猪和人类中引起严重且往往致命的疾病。目前尚无获批用于人类的疫苗或治疗方法。对尼帕病毒感染的小动物模型研究表明,抗体疗法可能是一种有前景的治疗方法。然而,大多数研究在病毒暴露后不久、动物出现疾病迹象之前就评估了治疗效果。我们在病毒暴露后的几个时间点,包括在尼帕病毒病统一致死的非人灵长类动物模型中临床疾病发作时,评估了一种全人源单克隆抗体m102.4的疗效。16只非洲绿猴经气管内接种致死剂量的尼帕病毒,12只动物在病毒攻击后第1、3或5天开始两次输注m102.4(15mg/kg),约2天后再次输注。病毒RNA、传染性病毒和/或尼帕病毒特异性免疫反应的存在表明,所有受试动物在攻击后均被感染。所有接受m102.4治疗的12只非洲绿猴均存活下来,而未治疗的对照动物在感染后第8至10天死于疾病。第5天治疗组的非洲绿猴出现了疾病临床症状,但所有动物在第16天前均康复。这些结果代表了一种研究性药物在非人灵长类动物中对尼帕病毒的成功体内治疗效果,并突出了单克隆抗体对一种高致病性人畜共患人类疾病可能产生的潜在影响。