A combinatorial approach of a polypharmacological adjuvant 2-deoxy-D-glucose with low dose radiation therapy to quell the cytokine storm in COVID-19 management.
Amit VermaAmitava AdhikaryGayle E WoloschakBilikere S DwarakanathRao V L PapineniPublished in: International journal of radiation biology (2020)
COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a pandemic disease and is the major cause of deaths worldwide. The clinical complexities (inflammation, cytokine storm, and multi-organ dysfunction) associated with COVID-19 poses constraints to effective management of critically ill COVID-19 patients. Low dose radiation therapy (LDRT) has been evaluated as a potential therapeutic modality for COVID-19 pneumonia. However, due to heterogeneity in disease manifestation and inter-individual variations, effective planning for LDRT is limited for this large-scale event. 2-deoxy-D-glucose (2-DG) has emerged as a polypharmacological agent for COVID-19 treatment due to its effects on the glycolytic pathway, anti-inflammatory action, and interaction with viral proteins. We suggest that 2-DG will be a potential adjuvant to enhance the efficacy of LDRT in the treatment of COVID-19 pneumonia. Withal, azido analog of 2-DG, 2-azido-2-DG can produce rapid catastrophic oxidative stress and quell the cytokine storm in critically ill COVID-19 patients.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- low dose
- oxidative stress
- radiation therapy
- early stage
- dna damage
- type diabetes
- blood glucose
- risk assessment
- intensive care unit
- adipose tissue
- insulin resistance
- combination therapy
- extracorporeal membrane oxygenation
- replacement therapy
- human health
- quantum dots