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Neutralizing antibodies for the prevention and treatment of COVID-19
- Source :
- Cellular and Molecular Immunology
- Publication Year :
- 2021
- Publisher :
- Springer Science and Business Media LLC, 2021.
-
Abstract
- Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) initiates the infection process by binding to the viral cellular receptor angiotensin-converting enzyme 2 through the receptor-binding domain (RBD) in the S1 subunit of the viral spike (S) protein. This event is followed by virus–cell membrane fusion mediated by the S2 subunit, which allows virus entry into the host cell. Therefore, the SARS-CoV-2 S protein is a key therapeutic target, and prevention and treatment of coronavirus disease 2019 (COVID-19) have focused on the development of neutralizing monoclonal antibodies (nAbs) that target this protein. In this review, we summarize the nAbs targeting SARS-CoV-2 proteins that have been developed to date, with a focus on the N-terminal domain and RBD of the S protein. We also describe the roles that binding affinity, neutralizing activity, and protection provided by these nAbs play in the prevention and treatment of COVID-19 and discuss the potential to improve nAb efficiency against multiple SARS-CoV-2 variants. This review provides important information for the development of effective nAbs with broad-spectrum activity against current and future SARS-CoV-2 strains.
- Subjects :
- Coronavirus disease 2019 (COVID-19)
medicine.drug_class
viruses
Protein subunit
Immunology
Review Article
Spike protein
Biology
Antibodies, Monoclonal, Humanized
Antibodies, Viral
Monoclonal antibody
Neutralization
Viral entry
medicine
Animals
Humans
Immunology and Allergy
Drug Approval
chemistry.chemical_classification
Clinical Trials as Topic
SARS-CoV-2
COVID-19
Lipid bilayer fusion
Antibodies, Neutralizing
Virology
COVID-19 Drug Treatment
Drug Combinations
Infectious Diseases
Enzyme
chemistry
Viral infection
Spike Glycoprotein, Coronavirus
biology.protein
Monoclonal antibodies
Immunotherapy
Antibody
Subjects
Details
- ISSN :
- 20420226 and 16727681
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Cellular & Molecular Immunology
- Accession number :
- edsair.doi.dedup.....52ee75ad7d2fc31bd5be2d4019c8caaa
- Full Text :
- https://doi.org/10.1038/s41423-021-00752-2