The HMOX1 Pathway as a Promising Target for the Treatment and Prevention of SARS-CoV-2 of 2019 (COVID-19).
Neelu BatraCristabelle De SouzaJyoti BatraAlan G RaetzAi-Ming YuPublished in: International journal of molecular sciences (2020)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- immune response
- endothelial cells
- anti inflammatory
- healthcare
- dendritic cells
- human health
- newly diagnosed
- ejection fraction
- minimally invasive
- prognostic factors
- protein protein
- signaling pathway
- early onset
- binding protein
- amino acid
- coronary artery disease
- cardiovascular events
- combination therapy
- primary care
- small molecule
- cardiovascular disease
- current status
- induced pluripotent stem cells
- patient reported
- antibiotic resistance genes
- smoking cessation