Ohashi Hirofumi, Watashi Koichi, Saso Wakana, Shionoya Kaho, Iwanami Shoya, Hirokawa Takatsugu, Shirai Tsuyoshi, Kanaya Shigehiko, Ito Yusuke, Kim Kwang Su, Nomura Takao, Suzuki Tateki, Nishioka Kazane, Ando Shuji, Ejima Keisuke, Koizumi Yoshiki, Tanaka Tomohiro, Aoki Shin, Kuramochi Kouji, Suzuki Tadaki, Hashiguchi Takao, Maenaka Katsumi, Matano Tetsuro, Muramatsu Masamichi, Saijo Masayuki, Aihara Kazuyuki, Iwami Shingo, Takeda Makoto, McKeating Jane A, Wakita Takaji
Department of Virology II, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Department of Applied Biological Science, Tokyo University of Science, Noda 278-8510, Japan.
iScience. 2021 Apr 23;24(4):102367. doi: 10.1016/j.isci.2021.102367. Epub 2021 Mar 26.
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 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.
迫切需要针对2019冠状病毒病的抗病毒治疗方法。我们在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的细胞培养模型中筛选了一组已获批的药物,并在VeroE6/TMPRSS2细胞中确定了两种抗病毒潜力高于瑞德西韦和氯喹等候选药物的新药物:抗炎药千金藤素和人类免疫缺陷病毒蛋白酶抑制剂奈非那韦。千金藤素通过阻断病毒与靶细胞的结合来抑制SARS-CoV-2进入,而奈非那韦则部分通过蛋白酶抑制来抑制病毒复制。与其不同的作用方式一致,这种联合治疗对限制SARS-CoV-2增殖的协同效应得到了凸显。结合肺中计算出的总药物浓度进行的抗病毒活性数学建模预测,奈非那韦将使病毒清除前的时间缩短4.9天,联合使用千金藤素/奈非那韦可增强其预测疗效。这些结果值得进一步评估千金藤素和奈非那韦潜在的抗SARS-CoV-2活性。