Elsevier

Immunology Letters

Volume 240, December 2021, Pages 1-8
Immunology Letters

Review
Targeting the PI3K/Akt/mTOR pathway: A therapeutic strategy in COVID-19 patients

https://doi.org/10.1016/j.imlet.2021.09.005Get rights and content

Highlights

  • Targeting the PI3K/Akt/mTOR pathway can potentially modulate the immune response in COVID-19.

  • Modulating the pathway can potentially mitigate thrombosis in COVID-19.

  • Inhibiting components of the pathway has the potential to reduce the viral load.

  • Different components in the pathway can be targeted at different stages.

Abstract

Some COVID-19 patients suffer complications from anti-viral immune responses which can lead to both a dangerous cytokine storm and development of blood-borne factors that render severe thrombotic events more likely. The precise immune response profile is likely, therefore, to determine and predict patient outcomes and also represents a target for intervention. Anti-viral T cell exhaustion in the early stages is associated with disease progression. Dysregulation of T cell functions, which precedes cytokine storm development and neutrophil expansion in alveolar tissues heralds damaging pathology.T cell function, cytokine production and factors that attract neutrophils to the lung can be modified through targeting molecules that can modulate T cell responses. Manipulating T cell responses by targeting the PI3K/Akt/mTOR pathway could provide the means to control the immune response in COVID-19 patients. During the initial anti-viral response, T cell effector function can be enhanced by delaying anti-viral exhaustion through inhibiting PI3K and Akt. Additionally, immune dysregulation can be addressed by enhancing immune suppressor functions by targeting downstream mTOR, an important intracellular modulator of cellular metabolism. Targeting this signalling pathway also has potential to prevent formation of thrombi due to its role in platelet activation. Furthermore, this signalling pathway is essential for SARS-cov-2 virus replication in host cells and its inhibition could, therefore, reduce viral load. The ultimate goal is to identify targets that can quickly control the immune response in COVID-19 patients to improve patient outcome. Targeting different levels of the PI3K/Akt/mTOR signalling pathway could potentially achieve this during each stage of the disease.

Keywords

COVID-19
PI3K
Akt
mTOR
Immune modulation
Thrombosis

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Rasha Abu-Eid: Dr Abu-Eid completed her PhD in Oral Pathology in 2005 from the University of Birmingham, England. After holding different positions in the University of Birmingham, University of Jordan and the University of Aberdeen, in 2011, she was successful in securing a research fellowship from the King Hussein Institute for Biotechnology and Cancer to conduct research in the field of cancer immunology in USA. In October 2016, she re-joined the University of Aberdeen as a Senior Lecturer in Oral Sciences and is currently the lead for cancer research at the Institute of Dentistry.

Frank James Ward: Frank Ward studied Immunology at King's College London and received his PhD from the University of London in 1996. He moved to the University of Aberdeen in 2000 to pursue his main research interest, which is to investigate how the immune system maintains immunological tolerance, particularly in autoimmune disease and cancer. During the last 10 years he has worked on the less well-studied soluble isoform of CTLA-4 as a potential checkpoint inhibitor target for a range of cancers. Frank has published data in several journals based on patient focused studies around sCTLA-4 and has presented at national and international conferences.

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