Highly Conserved Protective Epitopes on Influenza B Viruses

Cyrille Dreyfus(Scripps Research Institute), N.S. Laursen(Scripps Research Institute), Ted Kwaks(Janssen (Netherlands)), David Zuijdgeest(Janssen (Netherlands)), Reza Khayat(Scripps Research Institute), Damian C. Ekiert(Scripps Research Institute), Jeong Hyun Lee(Scripps Research Institute), Zoltan Metlagel(Scripps Research Institute), Miriam V. Bujny(Janssen (Netherlands)), Mandy Jongeneelen(Janssen (Netherlands)), Remko van der Vlugt(Janssen (Netherlands)), Mohammed Lamrani(Janssen (Netherlands)), Hans J. W. M. Korse(Janssen (Netherlands)), Eric Geelen(Janssen (Netherlands)), Özcan Sahin(Janssen (Netherlands)), Martijn Sieuwerts(Janssen (Netherlands)), Just P. J. Brakenhoff(Janssen (Netherlands)), Ronald Vogels(Janssen (Netherlands)), Olive T. W. Li(University of Hong Kong), Leo L. M. Poon(University of Hong Kong), Malik Peiris(University of Hong Kong), Wouter Koudstaal(Janssen (Netherlands)), Andrew B. Ward(Scripps Research Institute), Ian A. Wilson(Scripps Research Institute), Jaap Goudsmit(Janssen (Netherlands)), Robert H. Friesen(Janssen (Netherlands))
Science
August 10, 2012
Cited by 901Open Access
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Abstract

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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