Department of Microbiology, Boston University School of Medicine, Boston, MA 02118, USA.
Sci Transl Med. 2011 Oct 19;3(105):105ra103. doi: 10.1126/scitranslmed.3002901.
Hendra virus (HeV) is a recently emerged zoonotic paramyxovirus that can cause a severe and often fatal disease in horses and humans. HeV is categorized as a biosafety level 4 agent, which has made the development of animal models and testing of potential therapeutics and vaccines challenging. Infection of African green monkeys (AGMs) with HeV was recently demonstrated, and disease mirrored fatal HeV infection in humans, manifesting as a multisystemic vasculitis with widespread virus replication in vascular tissues and severe pathologic manifestations in the lung, spleen, and brain. Here, we demonstrate that m102.4, a potent HeV-neutralizing human monoclonal antibody (hmAb), can protect AGMs from disease after infection with HeV. Fourteen AGMs were challenged intratracheally with a lethal dose of HeV, and 12 subjects were infused twice with a 100-mg dose of m102.4 beginning at either 10, 24, or 72 hours after infection and again about 48 hours later. The presence of viral RNA, infectious virus, and HeV-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 on day 8 after infection. Animals in the 72-hour treatment group exhibited neurological signs of disease, but all animals started to recover by day 16 after infection. These results represent successful post-exposure in vivo efficacy by an investigational drug against HeV and highlight the potential impact a hmAb can have on human disease.
亨德拉病毒(HeV)是一种新近出现的人畜共患病副粘病毒,可导致马和人类患上严重且常常致命的疾病。HeV 被归类为生物安全 4 级制剂,这使得开发动物模型和测试潜在治疗方法和疫苗变得极具挑战性。最近有研究表明,非洲绿猴(AGM)感染了 HeV,其疾病与人类致命性 HeV 感染相似,表现为多系统血管炎,血管组织中广泛存在病毒复制,并在肺部、脾脏和大脑中出现严重的病理表现。在这里,我们证明 m102.4 是一种有效的 HeV 中和人源单克隆抗体(hmAb),可在 AGM 感染 HeV 后预防疾病。14 只 AGM 通过气管内接种致死剂量的 HeV 进行攻毒,12 只动物在感染后 10、24 或 72 小时开始,分两次给予 100mg 剂量的 m102.4 治疗,两次治疗间隔 48 小时。病毒 RNA、感染性病毒和 HeV 特异性免疫反应的存在表明,所有动物在攻毒后均被感染。接受 m102.4 治疗的 12 只 AGM 全部存活,而未接受治疗的对照组动物在感染后第 8 天死亡。在 72 小时治疗组的动物出现了疾病的神经症状,但所有动物在感染后第 16 天开始恢复。这些结果代表了一种研究性药物在 HeV 暴露后对动物的体内疗效,突出了人源单克隆抗体对人类疾病的潜在影响。