Neutralizing antibodies to block viral entry and for identification of entry inhibitors.


Journal

Antiviral research
ISSN: 1872-9096
Titre abrégé: Antiviral Res
Pays: Netherlands
ID NLM: 8109699

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 31 10 2023
revised: 01 02 2024
accepted: 07 02 2024
medline: 18 3 2024
pubmed: 19 2 2024
entrez: 18 2 2024
Statut: ppublish

Résumé

Neutralizing antibodies (NAbs) are naturally produced by our immune system to combat viral infections. Clinically, neutralizing antibodies with potent efficacy and high specificity have been extensively used to prevent and treat a wide variety of viral infections, including Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Human Immunodeficiency Virus (HIV), Dengue Virus (DENV) and Hepatitis B Virus (HBV). An overwhelmingly large subset of clinically effective NAbs operates by targeting viral envelope proteins to inhibit viral entry into the host cell. Binding of viral envelope protein to the host receptor is a critical rate limiting step triggering a cascade of downstream events, including endocytosis, membrane fusion and pore formation to allow viral entry. In recent years, improved structural knowledge on these processes have allowed researchers to also leverage NAbs as an indispensable tool in guiding discovery of novel antiviral entry inhibitors, providing drug candidates with high efficacy and pan-genus specificity. This review will summarize the latest progresses on the applications of NAbs as effective entry inhibitors and as important tools to develop antiviral therapeutics by high-throughput drug screenings, rational design of peptidic entry inhibitor mimicking NAbs and in silico computational modeling approaches.

Identifiants

pubmed: 38369246
pii: S0166-3542(24)00042-1
doi: 10.1016/j.antiviral.2024.105834
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Viral Envelope Proteins 0
Antiviral Agents 0
Antibodies, Viral 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

105834

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ee Hong Tam (EH)

School of Biological Sciences, Nanyang Technological University 637551, Singapore; Institute of Structural Biology, Nanyang Technological University 636921, Singapore.

Yu Peng (Y)

School of Biological Sciences, Nanyang Technological University 637551, Singapore; Institute of Structural Biology, Nanyang Technological University 636921, Singapore.

Megan Xin Yan Cheah (MXY)

Institute of Molecular and Cell Biology, A*STAR (Agency of Science, Technology and Research) 138673, Singapore.

Chuan Yan (C)

Institute of Molecular and Cell Biology, A*STAR (Agency of Science, Technology and Research) 138673, Singapore.

Tianshu Xiao (T)

School of Biological Sciences, Nanyang Technological University 637551, Singapore; Institute of Structural Biology, Nanyang Technological University 636921, Singapore. Electronic address: tianshu.xiao@ntu.edu.sg.

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Classifications MeSH