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奈非那韦在感染 SARS-CoV-2 的恒河猴和人类中的预防和治疗益处。

Preventive and therapeutic benefits of nelfinavir in rhesus macaques and human beings infected with SARS-CoV-2.

机构信息

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.

Drug Discovery and Design Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.

出版信息

Signal Transduct Target Ther. 2023 Apr 24;8(1):169. doi: 10.1038/s41392-023-01429-0.

Abstract

Effective drugs with broad spectrum safety profile to all people are highly expected to combat COVID-19 caused by SARS-CoV-2. Here we report that nelfinavir, an FDA approved drug for the treatment of HIV infection, is effective against SARS-CoV-2 and COVID-19. Preincubation of nelfinavir could inhibit the activity of the main protease of the SARS-CoV-2 (IC = 8.26 μM), while its antiviral activity in Vero E6 cells against a clinical isolate of SARS-CoV-2 was determined to be 2.93 μM (EC). In comparison with vehicle-treated animals, rhesus macaque prophylactically treated with nelfinavir had significantly lower temperature and significantly reduced virus loads in the nasal and anal swabs of the animals. At necropsy, nelfinavir-treated animals had a significant reduction of the viral replication in the lungs by nearly three orders of magnitude. A prospective clinic study with 37 enrolled treatment-naive patients at Shanghai Public Health Clinical Center, which were randomized (1:1) to nelfinavir and control groups, showed that the nelfinavir treatment could shorten the duration of viral shedding by 5.5 days (9.0 vs. 14.5 days, P = 0.055) and the duration of fever time by 3.8 days (2.8 vs. 6.6 days, P = 0.014) in mild/moderate COVID-19 patients. The antiviral efficiency and clinical benefits in rhesus macaque model and in COVID-19 patients, together with its well-established good safety profile in almost all ages and during pregnancy, indicated that nelfinavir is a highly promising medication with the potential of preventative effect for the treatment of COVID-19.

摘要

我们期待能够针对所有人群具有广谱安全性的有效药物来对抗由 SARS-CoV-2 引起的 COVID-19。在这里,我们报告说,奈非那韦是一种已获 FDA 批准用于治疗 HIV 感染的药物,对 SARS-CoV-2 有效,也能对抗 COVID-19。奈非那韦预孵育可抑制 SARS-CoV-2 的主要蛋白酶的活性(IC = 8.26 μM),而其在 Vero E6 细胞中针对 SARS-CoV-2 的临床分离株的抗病毒活性被确定为 2.93 μM(EC)。与用载体处理的动物相比,用奈非那韦预防性治疗的恒河猴的体温明显较低,并且动物的鼻腔和肛门拭子中的病毒载量明显降低。在尸检时,奈非那韦处理的动物肺部的病毒复制量减少了近三个数量级。一项在上海公共卫生临床中心进行的、有 37 名未经治疗的入组患者参与的前瞻性临床研究中,患者被随机(1:1)分为奈非那韦治疗组和对照组,研究表明奈非那韦治疗可以将病毒脱落的持续时间缩短 5.5 天(9.0 天比 14.5 天,P = 0.055),并将发热时间缩短 3.8 天(2.8 天比 6.6 天,P = 0.014)在轻症/中度 COVID-19 患者中。在恒河猴模型和 COVID-19 患者中的抗病毒效率和临床获益,以及在几乎所有年龄段和妊娠期间都具有良好的安全性,表明奈非那韦是一种很有前途的药物,具有预防 COVID-19 的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/324e/10126107/b92069c1dc0c/41392_2023_1429_Fig1_HTML.jpg

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