Published December 10, 2010 | Version v1
Journal article

Universal antibodies against the highly conserved influenza fusion peptide cross-neutralize several subtypes of influenza A virus

  • 1. Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON (Canada)
  • 2. Department of Microbiology, Faculty of Medicine, King Abdulaziz University, Jeddah (Saudi Arabia)
  • 3. Centre for Vaccine Evaluation, Biologics and Genetic Therapies Directorate, HPFB, Health Canada, Ottawa, ON (Canada)
  • 4. National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB (Canada)
  • 5. National Institute for the Control of Pharmaceutical and Biological Products, Beijing (China)
  • 6. Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Department of Medicine, Harvard Medical School, 44 Binney Street, Boston, MA 02115 (United States)

Description

Research highlights: → The fusion peptide is the only universally conserved epitope in all influenza viral hemagglutinins. → Anti-fusion peptide antibodies are universal antibodies that cross-react with all influenza HA subtypes. → The universal antibodies cross-neutralize different influenza A subtypes. → The universal antibodies inhibit the fusion process between the viruses and the target cells. -- Abstract: The fusion peptide of influenza viral hemagglutinin plays a critical role in virus entry by facilitating membrane fusion between the virus and target cells. As the fusion peptide is the only universally conserved epitope in all influenza A and B viruses, it could be an attractive target for vaccine-induced immune responses. We previously reported that antibodies targeting the first 14 amino acids of the N-terminus of the fusion peptide could bind to virtually all influenza virus strains and quantify hemagglutinins in vaccines produced in embryonated eggs. Here we demonstrate that these universal antibodies bind to the viral hemagglutinins in native conformation presented in infected mammalian cell cultures and neutralize multiple subtypes of virus by inhibiting the pH-dependant fusion of viral and cellular membranes. These results suggest that this unique, highly-conserved linear sequence in viral hemagglutinin is exposed sufficiently to be attacked by the antibodies during the course of infection and merits further investigation because of potential importance in the protection against diverse strains of influenza viruses.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2010.11.030

Additional details

Identifiers

DOI
10.1016/j.bbrc.2010.11.030;
PII
S0006-291X(10)02078-4;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
403
Journal Issue
2
Journal Page Range
p. 247-251
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45025621
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
AMINO ACIDS; CELL CULTURES; EGGS; HEMAGGLUTININS; INFLUENZA; INFLUENZA VIRUSES; PEPTIDES; PH VALUE; VACCINES
Descriptors DEC
AGGLUTININS; ANTIBODIES; CARBOXYLIC ACIDS; DISEASES; INFECTIOUS DISEASES; MICROORGANISMS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PARASITES; PROTEINS; VIRAL DISEASES; VIRUSES

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.