Back to Search
Start Over
Human monoclonal antibodies targeting the haemagglutinin glycoprotein can neutralize H7N9 influenza virus
- Source :
- Nature Communications. 6
- Publication Year :
- 2015
- Publisher :
- Springer Science and Business Media LLC, 2015.
-
Abstract
- The recently identified avian-originated influenza H7N9 virus causes severe pulmonary disease and may lead to death in humans. Currently, treatment options for the prevention and control of fatal H7N9 infections in humans remain limited. Here we characterize two human monoclonal antibodies (HuMAbs), HNIgGA6 and HNIgGB5, by screening a Fab antibody phage library derived from patients who recovered from H7N9 infection. Both antibodies exhibit high neutralizing activity against H7N9 virus in cells. Two amino acids in the receptor-binding site, 186V and 226L, are crucial for the binding of these two HuMAbs to viral haemagglutinin antigens. Prophylaxis with HNIgGA6 and HNIgGB5 confers significant immunity against H7N9 virus in a mouse model and significantly reduces the pulmonary virus titre. When administered post infection, therapeutic doses of the HuMAbs also provide robust protection against lethality. These antibodies might represent a potential alternative or adjunct to H7N9 pandemic interventions.
- Subjects :
- medicine.drug_class
General Physics and Astronomy
Hemagglutinin Glycoproteins, Influenza Virus
Antibodies, Viral
Influenza A Virus, H7N9 Subtype
medicine.disease_cause
Monoclonal antibody
General Biochemistry, Genetics and Molecular Biology
Virus
Mice
Orthomyxoviridae Infections
Antigen
Immunity
Influenza A virus
medicine
Animals
Humans
chemistry.chemical_classification
Multidisciplinary
biology
business.industry
Antibodies, Monoclonal
General Chemistry
Antibodies, Neutralizing
Virology
Titer
chemistry
Immunology
biology.protein
Antibody
Glycoprotein
business
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Nature Communications
- Accession number :
- edsair.doi.dedup.....51ea8ffdb85f8cade98ebee543b75be1
- Full Text :
- https://doi.org/10.1038/ncomms7714