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      Monocyte Distribution Width (MDW) as novel inflammatory marker with prognostic significance in COVID-19 patients

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          Abstract

          Monocyte Distribution Width (MDW), a new cytometric parameter correlating with cytomorphologic changes occurring upon massive monocyte activation, has recently emerged as promising early biomarker of sepsis. Similar to sepsis, monocyte/macrophage subsets are considered key mediators of the life-threatening hyper-inflammatory disorder characterizing severe COVID-19. In this study, we longitudinally analyzed MDW values in a cohort of 87 COVID-19 patients consecutively admitted to our hospital, showing significant correlations between MDW and common inflammatory markers, namely CRP ( p < 0.001), fibrinogen ( p < 0.001) and ferritin ( p < 0.01). Moreover, high MDW values resulted to be prognostically associated with fatal outcome in COVID-19 patients (AUC = 0.76, 95% CI: 0.66–0.87, sensitivity 0.75, specificity 0.70, MDW threshold 26.4; RR = 4.91, 95% CI: 1.73–13.96; OR = 7.14, 95% CI: 2.06–24.71). This pilot study shows that MDW can be useful in the monitoring of COVID-19 patients, as this innovative hematologic biomarker is: (1) easy to obtain, (2) directly related to the activation state of a fundamental inflammatory cell subset (i.e. monocytes, pivotal in both cytokine storm and sepsis immunopathogenesis), (3) well correlated with clinical severity of COVID-19-associated inflammatory disorder, and, in turn, (4) endowed with relevant prognostic significance. Additional studies are needed to define further the clinical impact of MDW testing in the management of COVID-19 patients.

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          Most cited references34

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          Clinical and immunologic features in severe and moderate Coronavirus Disease 2019

          Journal of Clinical Investigation
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            Single-cell landscape of bronchoalveolar immune cells in patients with COVID-19

            Respiratory immune characteristics associated with Coronavirus Disease 2019 (COVID-19) severity are currently unclear. We characterized bronchoalveolar lavage fluid immune cells from patients with varying severity of COVID-19 and from healthy people by using single-cell RNA sequencing. Proinflammatory monocyte-derived macrophages were abundant in the bronchoalveolar lavage fluid from patients with severe COVID-9. Moderate cases were characterized by the presence of highly clonally expanded CD8+ T cells. This atlas of the bronchoalveolar immune microenvironment suggests potential mechanisms underlying pathogenesis and recovery in COVID-19.
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              Pathological inflammation in patients with COVID-19: a key role for monocytes and macrophages

              The COVID-19 pandemic caused by infection with SARS-CoV-2 has led to more than 200,000 deaths worldwide. Several studies have now established that the hyperinflammatory response induced by SARS-CoV-2 is a major cause of disease severity and death in infected patients. Macrophages are a population of innate immune cells that sense and respond to microbial threats by producing inflammatory molecules that eliminate pathogens and promote tissue repair. However, a dysregulated macrophage response can be damaging to the host, as is seen in the macrophage activation syndrome induced by severe infections, including in infections with the related virus SARS-CoV. Here we describe the potentially pathological roles of macrophages during SARS-CoV-2 infection and discuss ongoing and prospective therapeutic strategies to modulate macrophage activation in patients with COVID-19.
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                Author and article information

                Contributors
                g.riva@ausl.mo.it
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                16 June 2021
                16 June 2021
                2021
                : 11
                : 12716
                Affiliations
                [1 ]Diagnostic Hematology and Clinical Genomics Laboratory, Department of Laboratory Medicine and Pathology, AUSL/AOU Policlinico, Via del Pozzo 71, 41124 Modena, Italy
                [2 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Medical and Surgical Sciences, , University of Modena and Reggio Emilia, ; Modena, Italy
                [3 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Medical and Surgical Sciences, , University of Modena and Reggio Emilia, Hematology Unit, AOU Policlinico, ; Modena, Italy
                [4 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Surgical, Medical, Dental and Morphological Sciences, , University of Modena and Reggio Emilia, ; Modena, Italy
                [5 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Anesthesia and Intensive Care, , University of Modena and Reggio Emilia, Intensive Care Unit, AOU Policlinico, ; Modena, Italy
                [6 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Surgical, Medical, Dental and Morphological Sciences, , University of Modena and Reggio Emilia, Infectious Diseases Clinics, AOU Policlinico, ; Modena, Italy
                [7 ]GRID grid.7548.e, ISNI 0000000121697570, Department of Life Sciences, , University of Modena and Reggio Emilia, Centre for Regenerative Medicine “Stefano Ferrari”, ; Modena, Italy
                Article
                92236
                10.1038/s41598-021-92236-6
                8209163
                34135448
                88330409-d4e7-41d4-96cc-96c7eba7582a
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 22 February 2021
                : 19 May 2021
                Categories
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                © The Author(s) 2021

                Uncategorized
                immunology,microbiology,biomarkers
                Uncategorized
                immunology, microbiology, biomarkers

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