Emerging small and large molecule therapeutics for respiratory syncytial virus

被引:19
作者
Bergeron, Harrison C. [1 ]
Tripp, Ralph A. [1 ]
机构
[1] Univ Georgia, Coll Vet Med, Dept Infect Dis, Athens, GA 30602 USA
关键词
Antibodies; antivirals; drug; inhibitor; monoclonal; respiratory syncytial virus; RSV; REPLICATION IN-VITRO; GLYCOPROTEIN MONOCLONAL-ANTIBODY; G-PROTEIN; PULMONARY INFLAMMATION; NEUTRALIZING EPITOPES; MATRIX PROTEIN; RSV INFECTION; SOLUBLE FORM; EBOLA-VIRUS; FUSION;
D O I
10.1080/13543784.2020.1735349
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Respiratory syncytial virus (RSV) causes lower respiratory tract infections and can lead to morbidity and mortality in the infant, elderly and immunocompromised. There is no vaccine and therapeutic interventions are limited. RSV disease research has yielded the development of several prophylactic and therapeutic treatments. Several promising candidates are currently under investigation. Areas covered: Small and large molecule approaches to RSV treatment were examined and categorized by their mechanism of action using data from PubMed, clinicaltrials.gov, and from the sponsoring organizations publicly available pipeline information. These results are prefaced by an overview of RSV to provide the context for rational therapy development. Expert opinion: While small molecule drugs show promise for RSV treatment, we believe that large molecule therapy using anti-RSV G and F protein monoclonal antibodies (mAbs) will most efficaciously and safely ameliorate RSV disease.
引用
收藏
页码:285 / 294
页数:10
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