A Neutralizing Human Monoclonal Antibody Protects African Green Monkeys from Hendra Virus Challenge

被引:98
作者
Bossart, Katharine N. [2 ,3 ]
Geisbert, Thomas W. [4 ,5 ]
Feldmann, Heinz [6 ,7 ]
Zhu, Zhongyu [8 ,9 ]
Feldmann, Friederike [10 ,11 ]
Geisbert, Joan B. [4 ,5 ]
Yan, Lianying [1 ]
Feng, Yan-Ru [1 ]
Brining, Doug [12 ]
Scott, Dana [12 ]
Wang, Yanping [8 ,9 ]
Dimitrov, Antony S. [13 ]
Callison, Julie [6 ]
Chan, Yee-Peng [1 ]
Hickey, Andrew C. [2 ,3 ]
Dimitrov, Dimiter S. [8 ]
Broder, Christopher C. [1 ]
Rockx, Barry [6 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
[2] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Natl Emerging Infect Dis Labs Inst, Boston, MA 02118 USA
[4] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX 77550 USA
[5] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[6] NIAID, Rocky Mt Labs, Virol Lab, NIH, Hamilton, MT 59840 USA
[7] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB R3T 2N2, Canada
[8] NCI, Prot Interact Grp, Ctr Canc Res, Nanobiol Program,NIH, Frederick, MD 21702 USA
[9] Frederick Inc, Sci Applicat Int Corp, Behav Res Program, Ft Detrick, MD 21702 USA
[10] NIAID, Rocky Mt Labs, Operat Off, NIH, Hamilton, MT 59840 USA
[11] NIAID, Rocky Mt Labs, Off Management, NIH, Hamilton, MT 59840 USA
[12] NIAID, Rocky Mt Labs, Rocky Mt Vet Branch, NIH, Hamilton, MT 59840 USA
[13] Profectus BioSci Inc, Baltimore, MD 21224 USA
关键词
NIPAH VIRUS; INFECTION; RECEPTOR; HENIPAVIRUS; BINDING; MODEL;
D O I
10.1126/scitranslmed.3002901
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:8
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