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      Multicenter, randomized controlled trial of traditional Japanese medicine, kakkonto with shosaikotokakikyosekko, for mild and moderate coronavirus disease patients

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          Abstract

          The traditional Japanese (Kampo) medicine, kakkonto with shosaikotokakikyosekko, has antiviral and anti-inflammatory effects. In this randomized trial, patients with mild and moderate coronavirus disease (COVID-19) were randomly allocated to the control group receiving conventional treatment for symptom relief such as antipyretics and antitussives or the Kampo group receiving mixed extract granules of kakkonto (2.5 g) and shosaikotokakikyosekko (2.5 g) three times a day for 14 days in addition to conventional treatment. The main outcome was the number of days until total symptom relief. The secondary outcome was the number of days until each symptom’s relief and whether the disease progressed to respiratory failure. We enrolled a total of 161 patients (Kampo group, n = 81; control group, n = 80). The results from Kaplan–Meier estimates of symptom relief showed that there are no significant differences between the groups. However, covariate-adjusted cumulative incidence of fever relief considering competitive risk showed that the recovery was significantly faster in the Kampo group than in the control group (HR 1.76, 95% CI 1.03–3.01). Additionally, the risk of disease progression to moderate COVID-19 requiring oxygen inhalation was lower in the Kampo group than in the control group (Risk Difference −0.13, 95% CI −0.27–0.01). No significant drug-related side effects were observed. Kakkonto with shosaikotokakikyosekko is effective for fever relief with suppression of disease progression in COVID-19 patients.

          Clinical Trial Registration: https://jrct.niph.go.jp/en-latest-detail/jRCTs021200020, identifier [jRCTs021200020]

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          SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

          Summary The recent emergence of the novel, pathogenic SARS-coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread pose a global health emergency. Cell entry of coronaviruses depends on binding of the viral spike (S) proteins to cellular receptors and on S protein priming by host cell proteases. Unravelling which cellular factors are used by SARS-CoV-2 for entry might provide insights into viral transmission and reveal therapeutic targets. Here, we demonstrate that SARS-CoV-2 uses the SARS-CoV receptor ACE2 for entry and the serine protease TMPRSS2 for S protein priming. A TMPRSS2 inhibitor approved for clinical use blocked entry and might constitute a treatment option. Finally, we show that the sera from convalescent SARS patients cross-neutralized SARS-2-S-driven entry. Our results reveal important commonalities between SARS-CoV-2 and SARS-CoV infection and identify a potential target for antiviral intervention.
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            Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention

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              Structure of Mpro from COVID-19 virus and discovery of its inhibitors

              A new coronavirus, known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the aetiological agent responsible for the 2019-2020 viral pneumonia outbreak of coronavirus disease 2019 (COVID-19)1-4. Currently, there are no targeted therapeutic agents for the treatment of this disease, and effective treatment options remain very limited. Here we describe the results of a programme that aimed to rapidly discover lead compounds for clinical use, by combining structure-assisted drug design, virtual drug screening and high-throughput screening. This programme focused on identifying drug leads that target main protease (Mpro) of SARS-CoV-2: Mpro is a key enzyme of coronaviruses and has a pivotal role in mediating viral replication and transcription, making it an attractive drug target for SARS-CoV-25,6. We identified a mechanism-based inhibitor (N3) by computer-aided drug design, and then determined the crystal structure of Mpro of SARS-CoV-2 in complex with this compound. Through a combination of structure-based virtual and high-throughput screening, we assayed more than 10,000 compounds-including approved drugs, drug candidates in clinical trials and other pharmacologically active compounds-as inhibitors of Mpro. Six of these compounds inhibited Mpro, showing half-maximal inhibitory concentration values that ranged from 0.67 to 21.4 μM. One of these compounds (ebselen) also exhibited promising antiviral activity in cell-based assays. Our results demonstrate the efficacy of our screening strategy, which can lead to the rapid discovery of drug leads with clinical potential in response to new infectious diseases for which no specific drugs or vaccines are available.
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                09 November 2022
                2022
                09 November 2022
                : 13
                : 1008946
                Affiliations
                [1] 1 Department of Education and Support for Regional Medicine (General and Kampo medicine) , Tohoku University Hospital , Sendai, Japan
                [2] 2 Department of Japanese-Oriental (Kampo) Medicine , Graduate School of Medicine , Chiba University , Chiba, Japan
                [3] 3 Department of Emergency and Critical Care Medicine , Akita University Graduate School of Medicine , Akita, Japan
                [4] 4 Department of Respiratory Medicine , Japanese Red Cross Ishinomaki Hospital , Ishinomaki, Japan
                [5] 5 Center for Kampo Medicine , Keio University School of Medicine , Tokyo, Japan
                [6] 6 Department of Cardiology , Yokohama City University Hospital , Yokohama, Japan
                [7] 7 Department of Traditional Medicine , Faculty of Medicine , Toho University , Tokyo, Japan
                [8] 8 Department of Cardiovascular Medicine , Tohoku University Graduate School of Medicine , Sendai, Japan
                [9] 9 Clinical Research Data Center , Tohoku University Hospital , Sendai, Japan
                [10] 10 Department of Neuropsychiatry , Keio University School of Medicine , Tokyo, Japan
                [11] 11 Division of Biostatistics , Tohoku University Graduate School of Medicine , Sendai, Japan
                [12] 12 Hospital Bando , Bando, Japan
                [13] 13 Medical Corporation Mitani Family Clinic , Osaka, Japan
                [14] 14 Akashi Clinic Kanda , Tokyo, Japan
                Author notes

                Edited by: Yonggang Zhang, Sichuan University, China

                Reviewed by: Abdelsamed I. Elshamy, National Research Centre, Egypt

                Oliviu Vostinaru, Iuliu HaÈ’ieganu University of Medicine and Pharmacy, Romania

                Niranjan Koirala, Gandaki Province Academy of Science and Technology, Nepal

                Haider Abdul-Lateef Mousa, University of Basrah, Iraq

                Patrick Okechukwu, UCSI University, Malaysia

                *Correspondence: Shin Takayama, takayama@ 123456med.tohoku.ac.jp

                This article was submitted to Drugs Outcomes Research and Policies, a section of the journal Frontiers in Pharmacology

                Article
                1008946
                10.3389/fphar.2022.1008946
                9682103
                40bb0bdf-8dbd-4882-a9d4-14ef4cc7aaa4
                Copyright © 2022 Takayama, Namiki, Arita, Ono, Kikuchi, Ohsawa, Saito, Suzuki, Nakae, Kobayashi, Yoshino, Ishigami, Tanaka, Nochioka, Takagi, Mimura, Yamaguchi, Ishii, Hisanaga, Mitani and Ito.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 August 2022
                : 07 October 2022
                Categories
                Pharmacology
                Clinical Trial

                Pharmacology & Pharmaceutical medicine
                kakkonto,shosaikotokakikyosekko,kampo medicines,covid-19,herbal medicine

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