Broadly neutralizing monoclonal antibodies protect against multiple tick-borne flaviviruses

被引:19
作者
VanBlargan, Laura A. [1 ]
Errico, John M. [2 ]
Kafai, Natasha M. [1 ,2 ]
Burgomaster, Katherine E. [3 ]
Jethva, Prashant N. [4 ]
Broeckel, Rebecca M. [5 ]
Meade-White, Kimberly [5 ]
Nelson, Christopher A. [2 ]
Himansu, Sunny [6 ]
Wang, David [7 ]
Handley, Scott A. [2 ]
Gross, Michael L. [4 ]
Best, Sonja M. [5 ]
Pierson, Theodore C. [3 ]
Fremont, Daved H. [2 ,7 ,8 ,9 ]
Diamond, Michael S. [1 ,2 ,7 ,9 ]
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63130 USA
[3] NIAID, Lab Viral Dis, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[4] Washington Univ, Dept Chem, St Louis, MO USA
[5] NIAID, Lab Virol, NIH, Hamilton, MT USA
[6] Moderna Inc, Cambridge, MA USA
[7] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[8] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
[9] Washington Univ, Andrew M & Jane M Bursky Ctr Human Immunol & Immu, Sch Med, St Louis, MO 63130 USA
基金
美国国家卫生研究院;
关键词
WEST-NILE; POWASSAN VIRUS; ENCEPHALITIS-VIRUS; MEDIATED NEUTRALIZATION; COXSACKIEVIRUS B3; STRUCTURAL BASIS; IN-VIVO; DETERMINANTS; RECEPTOR; PARTICLES;
D O I
10.1084/jem.20210174
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although Powassan virus (POWV) is an emerging tick-transmitted flavivirus that causes severe or fatal neuroinvasive disease in humans, medical countermeasures have not yet been developed. Here, we developed a panel of neutralizing anti-POWV mAbs recognizing six distinct antigenic sites. The most potent of these mAbs bind sites within domain II or III of the envelope (E) protein and inhibit postattachment viral entry steps. A subset of these mAbs cross-react with other flaviviruses. Both POWV type-specific and cross-reactive neutralizing mAbs confer protection in mice against POWV infection when given as prophylaxis or postexposure therapy. Several cross-reactive mAbs mapping to either domain II or III also protect in vivo against heterologous tick-transmitted flaviviruses including Langat and tick-borne encephalitis virus. Our experiments define structural and functional correlates of antibody protection against POWV infection and identify epitopes targeted by broadly neutralizing antibodies with therapeutic potential against multiple tick-borne flaviviruses.
引用
收藏
页数:28
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