scholarly journals Learning from the Past: Possible Urgent Prevention and Treatment Options for Severe Acute Respiratory Infections Caused by 2019‐nCoV

ChemBioChem ◽  
2020 ◽  
Vol 21 (5) ◽  
pp. 730-738 ◽  
Author(s):  
Jared S. Morse ◽  
Tyler Lalonde ◽  
Shiqing Xu ◽  
Wenshe Ray Liu
Author(s):  
Jared S. Morse ◽  
Tyler Lalonde ◽  
Shiqing Xu ◽  
Wenshe Liu

With the current trajectory of the 2019-nCoV outbreak unknown, public health and medicinal measures will both be needed to contain spreading of the virus and to optimize patient outcomes. While little is known about the virus, an examination of the genome sequence shows strong homology with its more well-studied cousin, SARS-CoV. The spike protein used for host cell infection shows key nonsynonymous mutations which may hamper efficacy of previously developed therapeutics but remains a viable target for the development of biologics and macrocyclic peptides. Other key drug targets, including RdRp and 3CLpro, share a strikingly high (>95%) homology to SARS-CoV. Herein, we suggest 4 potential drug candidates (an ACE2-based peptide, remdesivir, 3CLpro-1 and a novel vinylsulfone protease inhibitor) that can be used to treat patients suffering with the 2019-nCoV. We also summarize previous efforts into drugging these targets and hope to help in the development of broad spectrum anti-coronaviral agents for future epidemics.


Author(s):  
Jared S. Morse ◽  
Tyler Lalonde ◽  
Shiqing Xu ◽  
Wenshe Liu

With the current trajectory of the 2019-nCoV outbreak unknown, public health and medicinal measures will both be needed to contain spreading of the virus and to optimize patient outcomes. While little is known about the virus, an examination of the genome sequence shows strong homology with its more well-studied cousin, SARS-CoV. The spike protein used for host cell infection shows key nonsynonymous mutations which may hamper efficacy of previously developed therapeutics but remains a viable target for the development of biologics and macrocyclic peptides. Other key drug targets, including RdRp and 3CLpro, share a strikingly high (>95%) homology to SARS-CoV. Herein, we suggest 4 potential drug candidates (an ACE2-based peptide, remdesivir, 3CLpro-1 and a novel vinylsulfone protease inhibitor) that can be used to treat patients suffering with the 2019-nCoV. We also summarize previous efforts into drugging these targets and hope to help in the development of broad spectrum anti-coronaviral agents for future epidemics.


2021 ◽  
Vol 11 (4) ◽  
pp. 1696
Author(s):  
Mario Giosuè Balzanelli ◽  
Pietro Distratis ◽  
Orazio Catucci ◽  
Angelo Cefalo ◽  
Rita Lazzaro ◽  
...  

Due to the promising effects of mesenchymal stem cells (MSCs) in the treatment of various diseases, this commentary aimed to focus on the auxiliary role of MSCs to reduce inflammatory processes of acute respiratory infections caused by the 2019 novel coronavirus (COVID-19). Since early in 2020, COVID-19, a consequence of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has rapidly affected millions of people world-wide. The SARS-CoV-2 infection in children appears to be an unusual event. Despite the high number of affected adult and elderly, children and adolescents remained low in amounts, and marginally touched. Based on the promising role of cell therapy and regenerative medicine approaches in the treatment of several life-threatening diseases, it seems that applying MSCs cell-based approaches can also be a hopeful strategy for improving subjects with severe acute respiratory infections caused by COVID-19.


2015 ◽  
Vol 2 (suppl_1) ◽  
Author(s):  
Jorge Cortes ◽  
Liliana Diaz ◽  
Sandra Gomez ◽  
Alejandra Guarnizo ◽  
Tatiana Olarte ◽  
...  

2011 ◽  
Vol 65 (Suppl 1) ◽  
pp. A96-A96
Author(s):  
A. Cabello ◽  
M. V. Horoch ◽  
L. Bobadilla ◽  
C. Vazquez ◽  
M. Samudio ◽  
...  

2018 ◽  
Vol 1 (6) ◽  
pp. e47 ◽  
Author(s):  
Luiz Gustavo dos Anjos Borges ◽  
Adriana Giongo ◽  
Leandro de Mattos Pereira ◽  
Fernanda J. Trindade ◽  
Tatiana Schäffer Gregianini ◽  
...  

2021 ◽  
Vol 27 (1) ◽  
pp. 324-326
Author(s):  
Md R. Rahaman ◽  
Karen A. Alroy ◽  
Chris A. Van Beneden ◽  
Michael S. Friedman ◽  
Erin D. Kennedy ◽  
...  

2020 ◽  
Vol 26 (1) ◽  
pp. 148-150 ◽  
Author(s):  
Susana Monge ◽  
Janneke Duijster ◽  
Geert Jan Kommer ◽  
Jan van de Kassteele ◽  
Gé A. Donker ◽  
...  

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