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...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-06-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2021.697405/full |
id |
doaj-c8b9ff6dfb14423eb1d77f4157873d58 |
---|---|
record_format |
Article |
spelling |
doaj-c8b9ff6dfb14423eb1d77f4157873d582021-06-18T07:01:39ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-06-011210.3389/fimmu.2021.697405697405Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19Marianna Rowlands0Florencia Segal1Dominik Hartl2Dominik Hartl3Novartis Institutes for BioMedical Research (NIBR) Translational Medicine, Cambridge, MA, United StatesNovartis Institutes for BioMedical Research (NIBR) Translational Medicine, Cambridge, MA, United StatesNovartis Institutes for BioMedical Research (NIBR), Translational Medicine, Basel, SwitzerlandDepartment of Pediatrics I, University of Tübingen, Tübingen, GermanyClinical 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.https://www.frontiersin.org/articles/10.3389/fimmu.2021.697405/fullCOVID-19immunologyimmunityMDSCbiomarkers |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marianna Rowlands Florencia Segal Dominik Hartl Dominik Hartl |
spellingShingle |
Marianna Rowlands Florencia Segal Dominik Hartl Dominik Hartl Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 Frontiers in Immunology COVID-19 immunology immunity MDSC biomarkers |
author_facet |
Marianna Rowlands Florencia Segal Dominik Hartl Dominik Hartl |
author_sort |
Marianna Rowlands |
title |
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 |
title_short |
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 |
title_full |
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 |
title_fullStr |
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 |
title_full_unstemmed |
Myeloid-Derived Suppressor Cells as a Potential Biomarker and Therapeutic Target in COVID-19 |
title_sort |
myeloid-derived suppressor cells as a potential biomarker and therapeutic target in covid-19 |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2021-06-01 |
description |
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. |
topic |
COVID-19 immunology immunity MDSC biomarkers |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.697405/full |
work_keys_str_mv |
AT mariannarowlands myeloidderivedsuppressorcellsasapotentialbiomarkerandtherapeutictargetincovid19 AT florenciasegal myeloidderivedsuppressorcellsasapotentialbiomarkerandtherapeutictargetincovid19 AT dominikhartl myeloidderivedsuppressorcellsasapotentialbiomarkerandtherapeutictargetincovid19 AT dominikhartl myeloidderivedsuppressorcellsasapotentialbiomarkerandtherapeutictargetincovid19 |
_version_ |
1721373401366396928 |