The HMOX1 Pathway as a Promising Target for the Treatment and Prevention of SARS-CoV-2 of 2019 (COVID-19)

被引:32
作者
Batra, Neelu [1 ]
De Souza, Cristabelle [1 ,2 ]
Batra, Jyoti [3 ]
Raetz, Alan G. [1 ]
Yu, Ai-Ming [1 ]
机构
[1] UC Davis Sch Med, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[2] Univ New Mexico, Sch Med, Dept Internal Med, Canc Ctr, Albuquerque, NM 87131 USA
[3] Gladstone Inst, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
SARS-CoV-2; HMOX1; ORF3a; HMOX1-ORF3a; natural compounds; anti-viral therapy; MONOCLONAL-ANTIBODY RITUXIMAB; CYTOKINE-RELEASE SYNDROME; HEME OXYGENASE-1; CARBON-MONOXIDE; AZARDIRACHTA-INDICA; NLRP3; INFLAMMASOME; ANTIVIRAL ACTIVITY; LUNG INJURY; CELL-DEATH; INHIBITOR;
D O I
10.3390/ijms21176412
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The coronavirus disease of 2019 (COVID-19) or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is a global pandemic with increasing incidence and mortality rates. Recent evidence based on the cytokine profiles of severe COVID-19 cases suggests an overstimulation of macrophages and monocytes associated with reduced T-cell abundance (lymphopenia) in patients infected with SARS-CoV-2. The SARS-CoV-2 open reading frame 3 a (ORF3a) protein was found to bind to the human HMOX1 protein at a high confidence through high-throughput screening experiments. The HMOX1 pathway can inhibit platelet aggregation, and can have anti-thrombotic and anti-inflammatory properties, amongst others, all of which are critical medical conditions observed in COVID-19 patients. Here, we review the potential of modulating the HMOX1-ORF3a nexus to regulate the innate immune response for therapeutic benefits in COVID-19 patients. We also review other potential treatment strategies and suggest novel synthetic and natural compounds that may have the potential for future development in clinic.
引用
收藏
页码:1 / 16
页数:16
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