Repurposing Ivermectin for COVID-19: Molecular Aspects and Therapeutic Possibilities

dc.contributor.authorWehbe, Zena
dc.contributor.authorWehbe, Maya
dc.contributor.authorIratni, Rabah
dc.contributor.authorPintus, Gianfranco
dc.contributor.authorZaraket, Hassan
dc.contributor.authorYassine, Hadi M.
dc.contributor.authorEid, Ali H.
dc.contributor.departmentDepartment of Biology
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.departmentSpecialized Clinical Programs and Services
dc.contributor.departmentCenter for Infectious Diseases Research
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:21:09Z
dc.date.available2025-01-24T11:21:09Z
dc.date.issued2021
dc.description.abstractAs 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.
dc.identifier.doihttps://doi.org/10.3389/fimmu.2021.663586
dc.identifier.eid2-s2.0-85104070067
dc.identifier.pmid33859652
dc.identifier.urihttp://hdl.handle.net/10938/25219
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.relation.ispartofFrontiers in Immunology
dc.sourceScopus
dc.subjectCoronavirus
dc.subjectCovid-19
dc.subjectIvermectin
dc.subjectMechanism of action
dc.subjectSars-cov-2
dc.subjectActive transport, cell nucleus
dc.subjectAlpha karyopherins
dc.subjectAnimals
dc.subjectAntiviral agents
dc.subjectBeta karyopherins
dc.subjectCell line
dc.subjectChlorocebus aethiops
dc.subjectCoronavirus nucleocapsid proteins
dc.subjectDrug repositioning
dc.subjectHumans
dc.subjectPhosphoproteins
dc.subjectProtein transport
dc.subjectVero cells
dc.subjectVirus replication
dc.subjectAnakinra
dc.subjectAntiparasitic agent
dc.subjectAvermectin
dc.subjectAvermectin b1 a
dc.subjectCorticosteroid
dc.subjectDexamethasone
dc.subjectExoribonuclease
dc.subjectHydroxychloroquine
dc.subjectImportin alpha2 interacting protein alpha1
dc.subjectImportin alpha2 interacting protein b1
dc.subjectInterleukin 6
dc.subjectMessenger rna
dc.subjectMethyltransferase
dc.subjectNonstructural protein 1
dc.subjectNonstructural protein 2
dc.subjectNonstructural protein 3
dc.subjectNucleocapsid protein
dc.subjectNucleoporin
dc.subjectPapain-like protease
dc.subjectProtein
dc.subjectRna directed rna polymerase
dc.subjectTocilizumab
dc.subjectUbiquitin like n terminal domain 11
dc.subjectUnclassified drug
dc.subjectVirus spike protein
dc.subjectAntivirus agent
dc.subjectKaryopherin alpha
dc.subjectKaryopherin beta
dc.subjectNucleocapsid phosphoprotein, sars-cov-2
dc.subjectPhosphoprotein
dc.subjectAntiviral activity
dc.subjectApoptosis
dc.subjectAtaxia
dc.subjectBinding affinity
dc.subjectBlood brain barrier
dc.subjectBronchitis
dc.subjectClinical trial (topic)
dc.subjectComa
dc.subjectCoronavirus disease 2019
dc.subjectCytokine storm
dc.subjectCytotoxicity
dc.subjectDengue virus
dc.subjectDizziness
dc.subjectDna replication
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectFermentation
dc.subjectHeadache
dc.subjectHepatitis virus
dc.subjectHuman
dc.subjectHypoxia
dc.subjectImmunofluorescence
dc.subjectMiddle east respiratory syndrome coronavirus
dc.subjectMortality
dc.subjectNausea
dc.subjectNonhuman
dc.subjectPandemic
dc.subjectPathogenicity
dc.subjectReview
dc.subjectSpectroscopy
dc.subjectStreptomyces aureofaciens
dc.subjectTachycardia
dc.subjectTremor
dc.subjectVirus nucleocapsid
dc.subjectAnimal
dc.subjectDrug effect
dc.subjectDrug therapy
dc.subjectGrowth, development and aging
dc.subjectMetabolism
dc.subjectNucleocytoplasmic transport
dc.subjectVero cell line
dc.titleRepurposing Ivermectin for COVID-19: Molecular Aspects and Therapeutic Possibilities
dc.typeReview

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