Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19

Clinical presentations of COVID-19 are highly variable, yet the precise mechanisms that govern the pathophysiology of different disease courses remain poorly defined. Across the spectrum of disease severity, COVID-19 impairs both innate and adaptive host immune responses by activating innate immune cell recruitment, while resulting in low lymphocyte counts. Recently, several reports have shown that patients with severe COVID-19 exhibit a dysregulated myeloid cell compartment, with increased myeloid-derived suppressor cells (MDSCs) correlating with disease severity. MDSCs, in turn, promote virus survival by suppressing T-cell responses and driving a highly pro-inflammatory state through the secretion of various mediators of immune activation. Here, we summarize the evidence on MDSCs and myeloid cell dysregulation in COVID-19 infection and discuss the potential of MDSCs as biomarkers and therapeutic targets in COVID-19 pneumonia and associated disease.

Automated summary

The clinical presentations of COVID-19 are highly variable, and the pathophysiological mechanisms that govern different disease courses are still poorly understood. Severity of COVID-19 may be associated with dysregulation of myeloid-derived suppressor cells (MDSCs). MDSCs play a crucial role in COVID-19 infection by modulating T-cell responses and promoting an inflammatory state through secretion of mediators.