Structure of SARS-CoV-2 Spike Glycoprotein for Therapeutic and Preventive Target.
Jaewoo HongHyunjhung JhunYeo-Ok ChoiAfeisha S TaittSuyoung BaeYoungmin LeeChang-Seon SongSu Cheong YeomSoohyun KimPublished in: Immune network (2021)
The global crisis caused by the coronavirus disease 2019 (COVID-19) led to the most significant economic loss and human deaths after World War II. The pathogen causing this disease is a novel virus called the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). As of December 2020, there have been 80.2 million confirmed patients, and the mortality rate is known as 2.16% globally. A strategy to protect a host from SARS-CoV-2 is by suppressing intracellular viral replication or preventing viral entry. We focused on the spike glycoprotein that is responsible for the entry of SARS-CoV-2 into the host cell. Recently, the US Food and Drug Administration/EU Medicines Agency authorized a vaccine and antibody to treat COVID-19 patients by emergency use approval in the absence of long-term clinical trials. Both commercial and academic efforts to develop preventive and therapeutic agents continue all over the world. In this review, we present a perspective on current reports about the spike glycoprotein of SARS-CoV-2 as a therapeutic target.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- drug administration
- clinical trial
- public health
- end stage renal disease
- emergency department
- endothelial cells
- ejection fraction
- cardiovascular disease
- stem cells
- peritoneal dialysis
- prognostic factors
- mesenchymal stem cells
- randomized controlled trial
- cell therapy
- bone marrow
- open label
- patient reported outcomes
- phase iii
- drug induced