Highly Conserved Protective Epitopes on Influenza B Viruses

Author:

Dreyfus Cyrille1,Laursen Nick S.12,Kwaks Ted3,Zuijdgeest David3,Khayat Reza1,Ekiert Damian C.1,Lee Jeong Hyun1,Metlagel Zoltan1,Bujny Miriam V.3,Jongeneelen Mandy3,van der Vlugt Remko3,Lamrani Mohammed3,Korse Hans J. W. M.3,Geelen Eric3,Sahin Özcan3,Sieuwerts Martijn3,Brakenhoff Just P. J.3,Vogels Ronald3,Li Olive T. W.4,Poon Leo L. M.4,Peiris Malik4,Koudstaal Wouter3,Ward Andrew B.1,Wilson Ian A.15,Goudsmit Jaap3,Friesen Robert H. E.3

Affiliation:

1. Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

2. Department of Molecular Biology, Gustav Wieds Vej 10C, Aarhus 8000, Denmark.

3. Crucell Vaccine Institute, Janssen Center of Excellence for Immunoprophylaxis, Archimedesweg 4-6, 2301 CA Leiden, Netherlands.

4. State Key Laboratory of Emerging Infectious Diseases and School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong, China.

5. Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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