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suck abstract from ncbi


10.3390/v16010027

http://scihub22266oqcxt.onion/10.3390/v16010027
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38257728!10821470!38257728
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suck abstract from ncbi

pmid38257728      Viruses 2023 ; 16 (1): ?
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  • The Functional Roles of MDSCs in Severe COVID-19 Pathogenesis #MMPMID38257728
  • Len JS; Koh CWT; Chan KR
  • Viruses 2023[Dec]; 16 (1): ? PMID38257728show ga
  • Severe COVID-19 is a major cause of morbidity and mortality worldwide, especially among those with co-morbidities, the elderly, and the immunocompromised. However, the molecular determinants critical for severe COVID-19 progression remain to be fully elucidated. Meta-analyses of transcriptomic RNAseq and single-cell sequencing datasets comparing severe and mild COVID-19 patients have demonstrated that the early expansion of myeloid-derived suppressor cells (MDSCs) could be a key feature of severe COVID-19 progression. Besides serving as potential early prognostic biomarkers for severe COVID-19 progression, several studies have also indicated the functional roles of MDSCs in severe COVID-19 pathogenesis and possibly even long COVID. Given the potential links between MDSCs and severe COVID-19, we examine the existing literature summarizing the characteristics of MDSCs, provide evidence of MDSCs in facilitating severe COVID-19 pathogenesis, and discuss the potential therapeutic avenues that can be explored to reduce the risk and burden of severe COVID-19. We also provide a web app where users can visualize the temporal changes in specific genes or MDSC-related gene sets during severe COVID-19 progression and disease resolution, based on our previous study.
  • |*COVID-19[MESH]
  • |*Myeloid-Derived Suppressor Cells[MESH]
  • |Aged[MESH]
  • |Gene Expression Profiling[MESH]
  • |Humans[MESH]
  • |Immunocompromised Host[MESH]


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