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10.3389/fimmu.2021.663586

http://scihub22266oqcxt.onion/10.3389/fimmu.2021.663586
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suck abstract from ncbi


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pmid33859652      Front+Immunol 2021 ; 12 (ä): 663586
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  • Repurposing Ivermectin for COVID-19: Molecular Aspects and Therapeutic Possibilities #MMPMID33859652
  • Wehbe Z; Wehbe M; Iratni R; Pintus G; Zaraket H; Yassine HM; Eid AH
  • Front Immunol 2021[]; 12 (ä): 663586 PMID33859652show ga
  • 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.
  • |*COVID-19 Drug Treatment[MESH]
  • |Active Transport, Cell Nucleus/*drug effects[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/*therapeutic use[MESH]
  • |Cell Line[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus Nucleocapsid Proteins/antagonists & inhibitors/metabolism[MESH]
  • |Drug Repositioning[MESH]
  • |Humans[MESH]
  • |Ivermectin/*therapeutic use[MESH]
  • |Phosphoproteins/antagonists & inhibitors/metabolism[MESH]
  • |Protein Transport/drug effects[MESH]
  • |SARS-CoV-2/*drug effects/growth & development[MESH]
  • |Vero Cells[MESH]
  • |Virus Replication/drug effects[MESH]
  • |alpha Karyopherins/antagonists & inhibitors[MESH]


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