Remdesivir and Its Combination With Repurposed Drugs as COVID-19 Therapeutics

被引:11
作者
Chatterjee, Bhaswati [1 ]
Thakur, Suman S. [2 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Chem Sci, Hyderabad, India
[2] Ctr Cellular & Mol Biol, Prote & Cell Signaling, Hyderabad, India
关键词
repurposed drugs; therapeutics; COVID-19; remdesivir; baricitinib; DISEASE; 2019; COVID-19; CORONAVIRUS; BARICITINIB; INHIBITION; RUXOLITINIB; MECHANISM; INFECTION; OBATOCLAX;
D O I
10.3389/fimmu.2022.830990
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The SARS-CoV-2 virus needs multiple copies for its multiplication using an enzyme RNA-dependent RNA polymerase (RdRp). Remdesivir inhibits viral RdRp, controls the multiplication of the virus, and protects patients. However, treatment of COVID-19 with remdesivir involves adverse effects. Many ongoing clinical trials are exploring the potential of the combination of remdesivir with repurposed drugs by targeting multiple targets of virus and host human simultaneously. Better results were obtained with the remdesivir-baricitinib combination treatment for COVID-19 compared to the treatment with remdesivir alone. Notably, recovery from COVID-19 was found to be 8 days less via the remdesivir-baricitinib combination treatment as compared to remdesivir treatment alone. Furthermore, the mortality rate via the remdesivir-baricitinib combination treatment was lower compared to the remdesivir-only treatment. Remdesivir targets the SARS-CoV-2 enzyme while baricitinib targets the host human enzyme. Simultaneously, remdesivir and baricitinib as a combination inhibit their target viral RdRp and human Janus kinase, respectively. Ongoing trials for the combination of drugs will suggest in the future whether they may reduce the recovery time, reduce the mortality rate, and improve patient clinical status for noninvasive ventilation. In the future, simultaneously targeting virus replication enzymes and host human kinases may be the strategy for SARS-CoV-2 therapeutics.
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页数:13
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