表位
病毒学
单克隆抗体
生物
抗体
原罪
抗原漂移
H5N1基因结构
大流行
甲型流感病毒
抗原转移
病毒
免疫学
医学
2019年冠状病毒病(COVID-19)
传染病(医学专业)
疾病
病理
作者
Cyrille Dreyfus,Nick S. Laursen,Ted Kwaks,David Zuijdgeest,Reza Khayat,Damian C. Ekiert,Jeong Hyun Lee,Zoltan Metlagel,Miriam V. Bujny,Mandy Jongeneelen,Remko van der Vlugt,Mohammed Lamrani,Hans J. W. M. Korse,Eric Geelen,Özcan Sahin,Martijn Sieuwerts,Just P. J. Brakenhoff,Ronald Vogels,Olive T. W. Li,Leo L. M. Poon
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-08-10
卷期号:337 (6100): 1343-1348
被引量:802
标识
DOI:10.1126/science.1222908
摘要
Influenza Antibodies, Part B With its ability to reassort in animal hosts like pigs and birds, and to cause pandemics, influenza A viruses are often in the spotlight. However, a substantial portion of the annual flu burden is also the result of influenza B virus, which is a single influenza type that is characterized by two antigenically and genetically distinct lineages. Dreyfus et al. (p. 1343 , published online 9 August) identify three monoclonal human antibodies that are able to protect against lethal infection with both lineages of influenza B virus in mice. Two antibodies, which bind to distinct regions of the viral hemagluttinin (HA) molecule, neutralize multiple strains from both lineages of influenza B virus, whereas the third antibody binds to the stem region of HA and is able to neutralize both influenza A and B strains. The structural data from these antibodies bound to HA, together with already known antibodies targeting influenza A, may provide clues for designing a universal vaccine to protect against both influenza virus types.
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