Vaccination with prefusion-stabilized respiratory syncytial virus fusion protein elicits antibodies targeting a membrane-proximal epitope.
Respiratory syncytial virus (RSV) is the leading cause of bronchiolitis and pneumonia in infants, infecting all children by age 5. RSV also causes substantial morbidity and mortality in older adults, and a vaccine for older adults based on a prefusion-stabilized form of the viral F glycoprotein was recently approved by the FDA. Here, we investigate a set of antibodies that belong to the same public clonotype and were isolated from individuals vaccinated with a prefusion-stabilized RSV F protein. Our results reveal that these antibodies are highly potent and recognize a previously uncharacterized antigenic site on the prefusion F protein. Vaccination with prefusion RSV F proteins appears to boost the elicitation of these neutralizing antibodies, which are not commonly elicited by natural infection.
Duke Scholars
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Related Subject Headings
- Virology
- Viral Fusion Proteins
- Vaccination
- Respiratory Syncytial Virus, Human
- Respiratory Syncytial Virus Vaccines
- Respiratory Syncytial Virus Infections
- Humans
- Epitopes, B-Lymphocyte
- Antibodies, Viral
- Antibodies, Neutralizing
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Virology
- Viral Fusion Proteins
- Vaccination
- Respiratory Syncytial Virus, Human
- Respiratory Syncytial Virus Vaccines
- Respiratory Syncytial Virus Infections
- Humans
- Epitopes, B-Lymphocyte
- Antibodies, Viral
- Antibodies, Neutralizing