病毒学
登革热病毒
登革热
抗体
抗体依赖性增强
化学
生物
免疫学
作者
G. Fibriansah,Kristie D. Ibarra,Thiam‐Seng Ng,Scott A. Smith,Joanne L. Tan,Xin-Ni Lim,Justin S. G. Ooi,V.A. Kostyuchenko,Jiaqi Wang,Aravinda M. de Silva,Eva Harris,James E. Crowe,Shee‐Mei Lok
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2015-07-03
卷期号:349 (6243): 88-91
被引量:213
标识
DOI:10.1126/science.aaa8651
摘要
There are four closely-related dengue virus (DENV) serotypes. Infection with one serotype generates antibodies that may cross-react and enhance infection with other serotypes in a secondary infection. We demonstrated that DENV serotype 2 (DENV2)-specific human monoclonal antibody (HMAb) 2D22 is therapeutic in a mouse model of antibody-enhanced severe dengue disease. We determined the cryo-electron microscopy (cryo-EM) structures of HMAb 2D22 complexed with two different DENV2 strains. HMAb 2D22 binds across viral envelope (E) proteins in the dimeric structure, which probably blocks the E protein reorganization required for virus fusion. HMAb 2D22 "locks" two-thirds of or all dimers on the virus surface, depending on the strain, but neutralizes these DENV2 strains with equal potency. The epitope defined by HMAb 2D22 is a potential target for vaccines and therapeutics.
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