Repurposing Ivermectin for COVID-19: Molecular Aspects and Therapeutic Possibilities
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Frontiers Media S.A.
Abstract
As of January 2021, SARS-CoV-2 has killed over 2 million individuals across the world. As such, there is an urgent need for vaccines and therapeutics to reduce the burden of COVID-19. Several vaccines, including mRNA, vector-based vaccines, and inactivated vaccines, have been approved for emergency use in various countries. However, the slow roll-out of vaccines and insufficient global supply remains a challenge to turn the tide of the pandemic. Moreover, vaccines are important tools for preventing the disease but therapeutic tools to treat patients are also needed. As such, since the beginning of the pandemic, repurposed FDA-approved drugs have been sought as potential therapeutic options for COVID-19 due to their known safety profiles and potential anti-viral effects. One of these drugs is ivermectin (IVM), an antiparasitic drug created in the 1970s. IVM later exerted antiviral activity against various viruses including SARS-CoV-2. In this review, we delineate the story of how this antiparasitic drug was eventually identified as a potential treatment option for COVID-19. We review SARS-CoV-2 lifecycle, the role of the nucleocapsid protein, the turning points in past research that provided initial ‘hints’ for IVM’s antiviral activity and its molecular mechanism of action- and finally, we culminate with the current clinical findings. © Copyright © 2021 Wehbe, Wehbe, Iratni, Pintus, Zaraket, Yassine and Eid.
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Coronavirus, Covid-19, Ivermectin, Mechanism of action, Sars-cov-2, Active transport, cell nucleus, Alpha karyopherins, Animals, Antiviral agents, Beta karyopherins, Cell line, Chlorocebus aethiops, Coronavirus nucleocapsid proteins, Drug repositioning, Humans, Phosphoproteins, Protein transport, Vero cells, Virus replication, Anakinra, Antiparasitic agent, Avermectin, Avermectin b1 a, Corticosteroid, Dexamethasone, Exoribonuclease, Hydroxychloroquine, Importin alpha2 interacting protein alpha1, Importin alpha2 interacting protein b1, Interleukin 6, Messenger rna, Methyltransferase, Nonstructural protein 1, Nonstructural protein 2, Nonstructural protein 3, Nucleocapsid protein, Nucleoporin, Papain-like protease, Protein, Rna directed rna polymerase, Tocilizumab, Ubiquitin like n terminal domain 11, Unclassified drug, Virus spike protein, Antivirus agent, Karyopherin alpha, Karyopherin beta, Nucleocapsid phosphoprotein, sars-cov-2, Phosphoprotein, Antiviral activity, Apoptosis, Ataxia, Binding affinity, Blood brain barrier, Bronchitis, Clinical trial (topic), Coma, Coronavirus disease 2019, Cytokine storm, Cytotoxicity, Dengue virus, Dizziness, Dna replication, Drug efficacy, Drug safety, Fermentation, Headache, Hepatitis virus, Human, Hypoxia, Immunofluorescence, Middle east respiratory syndrome coronavirus, Mortality, Nausea, Nonhuman, Pandemic, Pathogenicity, Review, Spectroscopy, Streptomyces aureofaciens, Tachycardia, Tremor, Virus nucleocapsid, Animal, Drug effect, Drug therapy, Growth, development and aging, Metabolism, Nucleocytoplasmic transport, Vero cell line