群(周期表)
抗体
病毒学
A组
化学
微生物学
生物
免疫学
医学
内科学
有机化学
作者
Davide Corti,Jarrod Voss,S.J. Gamblin,Giosiana Codoni,Annalisa Macagno,David Jarrossay,S.G. Vachieri,Debora Pinna,Andrea Minola,Fabrizia Vanzetta,Chiara Silacci,Blanca Fernandez‐Rodriguez,Gloria Agatic,Siro Bianchi,Isabella Giacchetto-Sasselli,Lesley J. Calder,Federica Sallusto,Patrick Collins,L.F. Haire,Nigel Temperton
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2011-07-28
卷期号:333 (6044): 850-856
被引量:1225
标识
DOI:10.1126/science.1205669
摘要
The isolation of broadly neutralizing antibodies against influenza A viruses has been a long-sought goal for therapeutic approaches and vaccine design. Using a single-cell culture method for screening large numbers of human plasma cells, we isolated a neutralizing monoclonal antibody that recognized the hemagglutinin (HA) glycoprotein of all 16 subtypes and neutralized both group 1 and group 2 influenza A viruses. Passive transfer of this antibody conferred protection to mice and ferrets. Complexes with HAs from the group 1 H1 and the group 2 H3 subtypes analyzed by x-ray crystallography showed that the antibody bound to a conserved epitope in the F subdomain. This antibody may be used for passive protection and to inform vaccine design because of its broad specificity and neutralization potency.
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