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Promises and challenges of single-domain antibodies to control influenza.

Authors :
Matthys, Arne
Saelens, Xavier
Source :
Antiviral Research. Feb2024, Vol. 222, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

The World Health Organization advices the use of a quadrivalent vaccine as prophylaxis against influenza, to prevent severe influenza-associated disease and -mortality, and to keep up with influenza antigenic diversity. Different small molecule antivirals to treat influenza have become available. However, emergence of drug resistant influenza viruses has been observed upon use of these antivirals. An appealing alternative approach to prevent or treat influenza is the use of antibody-based antivirals, such as conventional monoclonal antibodies and single-domain antibodies (sdAbs). The surface of the influenza A and B virion is decorated with hemagglutinin molecules, which act as receptor-binding and membrane fusion proteins and represent the main target of neutralizing antibodies. SdAbs that target influenza A and B hemagglutinin have been described. In addition, sdAbs directed against the influenza A virus neuraminidase have been reported, whereas no sdAbs targeting influenza B neuraminidase have been described to date. SdAbs directed against influenza A matrix protein 2 or its ectodomain have been reported, while no sdAbs have been described targeting the influenza B matrix protein 2. Known for their high specificity, ease of production and formatting, sdAb-based antivirals could be a major leap forward in influenza control. [Display omitted] • SdAb against influenza HA, NA and M2 are described. • SdAbs formatted into multivalent constructs increase breadth and potency against IAV and IBV. • SdAbs have advantages over monoclonals in influenza virus control. • Anti-influenza sdAbs together with recent innovations could improve influenza virus control. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01663542
Volume :
222
Database :
Academic Search Index
Journal :
Antiviral Research
Publication Type :
Academic Journal
Accession number :
175296420
Full Text :
https://doi.org/10.1016/j.antiviral.2024.105807