Promises and challenges of single-domain antibodies to control influenza

被引:1
|
作者
Matthys, Arne [1 ,2 ]
Saelens, Xavier [1 ,2 ]
机构
[1] VIB Ctr Med Biotechnol VIB, Ghent, Belgium
[2] Univ Ghent, Dept Biochem & Microbiol, Ghent, Belgium
关键词
Single -domain antibody; Hemagglutinin; Neuraminidase; Matrix protein 2; VIRUS M2 PROTEIN; ION-CHANNEL; ADAMANTANE RESISTANCE; TRANSMEMBRANE DOMAIN; B VIRUS; INFECTION; NEURAMINIDASE; TRANSMISSION; OSELTAMIVIR; NANOBODIES;
D O I
10.1016/j.antiviral.2024.105807
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
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页数:15
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