A treatment for and vaccine against the deadly Hendra and Nipah viruses

被引:92
作者
Broder, Christopher C. [1 ]
Xu, Kai [2 ]
Nikolov, Dimitar B. [2 ]
Zhu, Zhongyu [3 ]
Dimitrov, Dimiter S. [3 ]
Middleton, Deborah [4 ]
Pallister, Jackie [4 ]
Geisbert, Thomas W. [5 ,6 ]
Bossart, Katharine N. [7 ,8 ]
Wang, Lin-Fa [4 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
[2] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10021 USA
[3] NCI, Prot Interact Grp, NIH, Frederick, MD 21702 USA
[4] CSIRO Livestock Ind, Australian Anim Hlth Lab, Geelong, Vic, Australia
[5] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[6] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX 77550 USA
[7] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[8] Boston Univ, Sch Med, Natl Emerging Infect Dis Labs Inst, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
Hendra virus; Nipah virus; Vaccine; Monoclonal antibody; G glycoprotein; Horse; G-GLYCOPROTEIN; HAMSTER MODEL; INFECTION; RIBAVIRIN; FUSION; ENCEPHALITIS; PROTECTION; ANTIBODIES; CHALLENGE; CANDIDATE;
D O I
10.1016/j.antiviral.2013.06.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hendra virus and Nipah virus are bat-borne paramyxoviruses that are the prototypic members of the genus Henipavirus. The henipaviruses emerged in the 1990s, spilling over from their natural bat hosts and causing serious disease outbreaks in humans and livestock. Hendra virus emerged in Australia and since 1994 there have been 7 human infections with 4 case fatalities. Nipah virus first appeared in Malaysia and subsequent outbreaks have occurred in Bangladesh and India. In total, there have been an estimated 582 human cases of Nipah virus and of these, 54% were fatal. Their broad species tropism and ability to cause fatal respiratory and/or neurologic disease in humans and animals make them important transboundary biological threats. Recent experimental findings in animals have demonstrated that a human monoclonal antibody targeting the viral G glycoprotein is an effective post-exposure treatment against Hendra and Nipah virus infection. In addition, a subunit vaccine based on the G glycoprotein of Hendra virus affords protection against Hendra and Nipah virus challenge. The vaccine has been developed for use in horses in Australia and is the first vaccine against a Biosafety Level-4 (BSL-4) agent to be licensed and commercially deployed. Together, these advances offer viable approaches to address Hendra and Nipah virus infection of livestock and people. Published by Elsevier B.V.
引用
收藏
页码:8 / 13
页数:6
相关论文
共 58 条
[1]  
Abdullah S, 2012, NEUROL ASIA, V17, P71
[2]   Henipavirus Membrane Fusion and Viral Entry [J].
Aguilar, Hector C. ;
Iorio, Ronald M. .
HENIPAVIRUS: ECOLOGY, MOLECULAR VIROLOGY, AND PATHOGENESIS, 2012, 359 :79-94
[3]   Characteristics of Nipah virus and Hendra virus replication in different cell lines and their suitability for antiviral screening [J].
Aljofan, Mohamad ;
Saubern, Simon ;
Meyer, Adam G. ;
Marsh, Glenn ;
Meers, Joanne ;
Mungall, Bruce A. .
VIRUS RESEARCH, 2009, 142 (1-2) :92-99
[4]  
[Anonymous], 2009, HENDRA VIRUS HUMAN E
[5]  
[Anonymous], 2013, HENDRA VIRUS
[6]  
[Anonymous], 2013, HENDRA VIRUS EQUINE
[7]  
[Anonymous], 2013, NIPAH ENCEPHALITIS H
[8]  
[Anonymous], 2012, HENDRA VIRUS EQUINE
[9]  
[Anonymous], 2010, HENDRA VIRUS EQUINE
[10]  
Balzer M, 2011, AUST VET J, V89, pN2