Single-Domain Antibodies as Therapeutics for Respiratory RNA Virus Infections

被引:5
|
作者
Huang, Keke [1 ]
Ying, Tianlei [1 ,2 ]
Wu, Yanling [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, MOE NHC Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
[2] Shanghai Engn Res Ctr Synthet Immunol, Shanghai 200032, Peoples R China
来源
VIRUSES-BASEL | 2022年 / 14卷 / 06期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
single-domain antibody; nanobody; respiratory RNA virus; antiviral therapeutics; inhalable property; INFLUENZA INFECTION; NEUTRALIZATION; SARS-COV-2; NANOBODIES; PROTECT; POTENT; MECHANISMS; EXPRESSION; INSIGHTS; RECEPTOR;
D O I
10.3390/v14061162
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Over the years, infectious diseases with high morbidity and mortality disrupted human healthcare systems and devastated economies globally. Respiratory viruses, especially emerging or re-emerging RNA viruses, including influenza and human coronavirus, are the main pathogens of acute respiratory diseases that cause epidemics or even global pandemics. Importantly, due to the rapid mutation of viruses, there are few effective drugs and vaccines for the treatment and prevention of these RNA virus infections. Of note, a class of antibodies derived from camelid and shark, named nanobody or single-domain antibody (sdAb), was characterized by smaller size, lower production costs, more accessible binding epitopes, and inhalable properties, which have advantages in the treatment of respiratory diseases compared to conventional antibodies. Currently, a number of sdAbs have been developed against various respiratory RNA viruses and demonstrated potent therapeutic efficacy in mouse models. Here, we review the current status of the development of antiviral sdAb and discuss their potential as therapeutics for respiratory RNA viral diseases.
引用
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页数:21
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