Human gene polymorphisms and their possible impact on the clinical outcome of SARS-CoV-2 infection
- 2 May 2021
- journal article
- review article
- Published by Springer Nature in Archives of Virology
- Vol. 166 (8) , 2089-2108
Abstract
The SARS-CoV-2 pandemic has become one of the most serious health concerns globally. Although multiple vaccines have recently been approved for the prevention of coronavirus disease 2019 (COVID-19), an effective treatment is still lacking. Our knowledge of the pathogenicity of this virus is still incomplete. Studies have revealed that viral factors such as the viral load, duration of exposure to the virus, and viral mutations are important variables in COVID-19 outcome. Furthermore, host factors, including age, health condition, co-morbidities, and genetic background, might also be involved in clinical manifestations and infection outcome. This review focuses on the importance of variations in the host genetic background and pathogenesis of SARS-CoV-2. We will discuss the significance of polymorphisms in the ACE-2, TMPRSS2, vitamin D receptor, vitamin D binding protein, CD147, glucose‐regulated protein 78 kDa, dipeptidyl peptidase-4 (DPP4), neuropilin-1, heme oxygenase, apolipoprotein L1, vitamin K epoxide reductase complex 1 (VKORC1), and immune system genes for the clinical outcome of COVID-19.Keywords
Funding Information
- Shiraz University of Medical Sciences (22169)
This publication has 219 references indexed in Scilit:
- Structure of MERS-CoV spike receptor-binding domain complexed with human receptor DPP4Cell Research, 2013
- Apolipoprotein L6, Induced in Atherosclerotic Lesions, Promotes Apoptosis and Blocks Beclin 1-dependent Autophagy in Atherosclerotic CellsJournal of Biological Chemistry, 2011
- The Vitamin D Receptor: New Paradigms for the Regulation of Gene Expression by 1,25-Dihydroxyvitamin D3Endocrinology and Metabolism Clinics of North America, 2010
- The Cytoplasmic Peptidase DPP9 Is Rate-limiting for Degradation of Proline-containing PeptidesJournal of Biological Chemistry, 2009
- Severe Respiratory Disease Concurrent with the Circulation of H1N1 InfluenzaNew England Journal of Medicine, 2009
- Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer DiseaseThe American Journal of Human Genetics, 2009
- Apolipoprotein L1, a Novel Bcl-2 Homology Domain 3-only Lipid-binding Protein, Induces Autophagic Cell DeathJournal of Biological Chemistry, 2008
- The evolutionary history of the CD209 (DC-SIGN) family in humans and non-human primatesGenes & Immunity, 2008
- CD147 immunoglobulin superfamily receptor function and role in pathologyExperimental and Molecular Pathology, 2007
- Polymorphisms in interferon-induced genes and the outcome of hepatitis C virus infection: roles of MxA, OAS-1 and PKRGenes & Immunity, 2003