TY - JOUR
T1 - Repurposing Ivermectin for COVID-19
T2 - Molecular Aspects and Therapeutic Possibilities
AU - Wehbe, Zena
AU - Wehbe, Maya
AU - Iratni, Rabah
AU - Pintus, Gianfranco
AU - Zaraket, Hassan
AU - Yassine, Hadi M.
AU - Eid, Ali H.
N1 - Funding Information:
This study was supported by Qatar University Grants # QUCG-BRC-20_21 and QUHI-BRC-20/21-1.
Publisher Copyright:
© Copyright © 2021 Wehbe, Wehbe, Iratni, Pintus, Zaraket, Yassine and Eid.
PY - 2021/3/30
Y1 - 2021/3/30
N2 - 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.
AB - 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.
KW - COVID-19
KW - SARS-CoV-2
KW - coronavirus
KW - ivermectin
KW - mechanism of action
UR - http://www.scopus.com/inward/record.url?scp=85104070067&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85104070067&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2021.663586
DO - 10.3389/fimmu.2021.663586
M3 - Review article
C2 - 33859652
AN - SCOPUS:85104070067
SN - 1664-3224
VL - 12
JO - Frontiers in immunology
JF - Frontiers in immunology
M1 - 663586
ER -