| Literature DB >> 33817567 |
Hirofumi Ohashi1,2, Koichi Watashi1,2,3,4,5, Wakana Saso1,6,7, Kaho Shionoya1,2, Shoya Iwanami8, Takatsugu Hirokawa9,10,11, Tsuyoshi Shirai12, Shigehiko Kanaya13, Yusuke Ito8, Kwang Su Kim8, Takao Nomura14, Tateki Suzuki15, Kazane Nishioka1,2, Shuji Ando16, Keisuke Ejima17, Yoshiki Koizumi18, Tomohiro Tanaka19, Shin Aoki19,20, Kouji Kuramochi2, Tadaki Suzuki21, Takao Hashiguchi15, Katsumi Maenaka14,22,23, Tetsuro Matano6,7, Masamichi Muramatsu1, Masayuki Saijo16, Kazuyuki Aihara24, Shingo Iwami4,8,25,26,27, Makoto Takeda28, Jane A McKeating29, Takaji Wakita1.
Abstract
Antiviral treatments targeting the coronavirus disease 2019 are urgently required. We screened a panel of already approved drugs in a cell culture model of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and identified two new agents having higher antiviral potentials than the drug candidates such as remdesivir and chroloquine in VeroE6/TMPRSS2 cells: the anti-inflammatory drug cepharanthine and human immunodeficiency virus protease inhibitor nelfinavir. Cepharanthine inhibited SARS-CoV-2 entry through the blocking of viral binding to target cells, while nelfinavir suppressed viral replication partly by protease inhibition. Consistent with their different modes of action, synergistic effect of this combined treatment to limit SARS-CoV-2 proliferation was highlighted. Mathematical modeling in vitro antiviral activity coupled with the calculated total drug concentrations in the lung predicts that nelfinavir will shorten the period until viral clearance by 4.9 days and the combining cepharanthine/nelfinavir enhanced their predicted efficacy. These results warrant further evaluation of the potential anti-SARS-CoV-2 activity of cepharanthine and nelfinavir.Entities:
Keywords: Medical Substance; Pharmaceutical Preparation; Virology
Year: 2021 PMID: 33817567 PMCID: PMC7997640 DOI: 10.1016/j.isci.2021.102367
Source DB: PubMed Journal: iScience ISSN: 2589-0042