PI3K/Akt/mTOR pathway: a potential target for anti-SARS-CoV-2 therapy
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Soheila Fattahi1, Zahra Khalifehzadeh-Esfahani2, Mina Mohammad-Rezaei3,4
1Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Abstract:
Coronavirus disease 2019 (COVID-19) is a viral infection caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). A single-stranded RNA virus from a β-Coronaviridae family causes acute clinical manifestations. Its high death rate and severe clinical symptoms have turned it into the most significant challenge worldwide. Up until now, several effective COVID-19 vaccines have been designed and marketed, but our data on specialized therapeutic drugs for the treatment of COVID-19 is still limited. In order to synthesis virus particles, SARS-CoV-2 uses host metabolic pathways such as phosphoinositide3-kinase (PI3K)/protein kinase B (PKB, also known as AKT)/mammalian target of rapamycin (mTOR). mTOR is involved in multiple biological processes. Over-activation of the mTOR pathway improves viral replication, which makes it a possible target in COVID-19 therapy. Clinical data shows the hyperactivation of the mTOR pathway in lung tissues during respiratory viral infections. However, the exact impact of mTOR pathway inhibitors on the COVID-19 severity and death rate is yet to be thoroughly investigated. There are several mTOR pathway inhibitors. Rapamycin is the most famous inhibitor of mTORC1 among all. Studies on other respiratory viruses suggest that the therapeutic inhibitors of the mTOR pathway, especially rapamycin, can be a potential approach to anti-SARS-CoV-2 therapy. Using therapeutic methods that inhibit harmful immune responses can open a new chapter in treating severe COVID-19 disease. We highlighted the potential contribution of PI3K/Akt/mTOR inhibitors in the treatment of COVID-19.
Insights
The mammalian target of rapamycin (mTOR) pathway is crucial for SARS-CoV-2 replication. Inhibiting this pathway, particularly with rapamycin, shows promise for treating severe COVID-19 by modulating harmful immune responses.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Coronavirus disease 2019 (COVID-19), caused by SARS-CoV-2, presents a significant global health challenge with limited therapeutic options beyond vaccines.
- The virus hijacks host metabolic pathways, including the PI3K/Akt/mTOR pathway, for replication.
Purpose of the Study:
- To explore the potential of inhibiting the PI3K/Akt/mTOR pathway as a therapeutic strategy against SARS-CoV-2.
- To investigate the role of mTOR pathway hyperactivation in COVID-19 severity.
Main Methods:
- Review of existing clinical data and studies on respiratory viral infections.
- Analysis of the function of the mTOR pathway in viral replication and host immune response.
Main Results:
- The mTOR pathway is hyperactivated in lung tissues during respiratory viral infections, including COVID-19.
- Over-activation of mTOR enhances viral replication, identifying it as a potential therapeutic target.
- Studies on other respiratory viruses suggest mTOR inhibitors, like rapamycin, may be effective against SARS-CoV-2.
Conclusions:
- Inhibitors of the PI3K/Akt/mTOR pathway represent a promising therapeutic avenue for COVID-19 treatment.
- Targeting harmful immune responses via mTOR inhibition could offer a new approach to managing severe COVID-19.
- Further investigation into the precise impact of mTOR inhibitors on COVID-19 outcomes is warranted.
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