Literature DB >> 33617030

Flow cytometric evaluation of the neutrophil compartment in COVID-19 at hospital presentation: A normal response to an abnormal situation.

Roy Spijkerman1,2,3, Suzanne H Bongers2,3, Bas J J Bindels1,3, Gerjen H Tinnevelt4, Giulio Giustarini1,3, Nikita K N Jorritsma1,3, Wiebe Buitenwerf1,3, Daan E J van Spengler1,3, Eveline M Delemarre3, Stefan Nierkens3, Harriët M R van Goor5, Jeroen J Jansen4, Nienke Vrisekoop1,3, Falco Hietbrink2, Luke P H Leenen2, Karin A H Kaasjager5, Leo Koenderman1,3.   

Abstract

Coronavirus disease 2019 (COVID-19) is a rapidly emerging pandemic disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Critical COVID-19 is thought to be associated with a hyper-inflammatory process that can develop into acute respiratory distress syndrome, a critical disease normally mediated by dysfunctional neutrophils. This study tested the hypothesis whether the neutrophil compartment displays characteristics of hyperinflammation in COVID-19 patients. Therefore, a prospective study was performed on all patients with suspected COVID-19 presenting at the emergency room of a large academic hospital. Blood drawn within 2 d after hospital presentation was analyzed by point-of-care automated flow cytometry and compared with blood samples collected at later time points. COVID-19 patients did not exhibit neutrophilia or eosinopenia. Unexpectedly neutrophil activation markers (CD11b, CD16, CD10, and CD62L) did not differ between COVID-19-positive patients and COVID-19-negative patients diagnosed with other bacterial/viral infections, or between COVID-19 severity groups. In all patients, a decrease was found in the neutrophil maturation markers indicating an inflammation-induced left shift of the neutrophil compartment. In COVID-19 this was associated with disease severity. ©2020 Society for Leukocyte Biology.

Entities:  

Keywords:  CD10; SARS‐CoV‐2; activation; flow cytometry; neprilysin; neutrophil

Year:  2021        PMID: 33617030     DOI: 10.1002/JLB.5COVA0820-520RRR

Source DB:  PubMed          Journal:  J Leukoc Biol        ISSN: 0741-5400            Impact factor:   4.962


  8 in total

1.  Differential Functional Responses of Neutrophil Subsets in Severe COVID-19 Patients.

Authors:  Kenneth R McLeish; Rejeena Shrestha; Aruna Vashishta; Madhavi J Rane; Michelle T Barati; Michael E Brier; Mario Gutierrez Lau; Xiaoling Hu; Oscar Chen; Caitlin R Wessel; Travis Spalding; Sarah E Bush; Kenechi Ijemere; C Danielle Hopkins; Elizabeth A Cooke; Shweta Tandon; Terri Manning; Silvia M Uriarte; Jiapeng Huang; Jun Yan
Journal:  Front Immunol       Date:  2022-05-31       Impact factor: 8.786

2.  Impairment of neutrophil functions and homeostasis in COVID-19 patients: association with disease severity.

Authors:  Chloé Loyer; Arnaud Lapostolle; Tomas Urbina; Alexandre Elabbadi; Jean-Rémi Lavillegrand; Thomas Chaigneau; Coraly Simoes; Julien Dessajan; Cyrielle Desnos; Mélanie Morin-Brureau; Yannick Chantran; Pierre Aucouturier; Bertrand Guidet; Guillaume Voiriot; Hafid Ait-Oufella; Carole Elbim
Journal:  Crit Care       Date:  2022-05-30       Impact factor: 19.334

Review 3.  New Discovery of Myeloid-Derived Suppressor Cell's Tale on Viral Infection and COVID-19.

Authors:  Soo-Jeung Park; Da-Eun Nam; Hae Chang Seong; Young S Hahn
Journal:  Front Immunol       Date:  2022-02-03       Impact factor: 7.561

4.  Severe COVID-19 is characterised by inflammation and immature myeloid cells early in disease progression.

Authors:  Liam Townsend; Adam H Dyer; Aifric Naughton; Sultan Imangaliyev; Jean Dunne; Rachel Kiersey; Dean Holden; Aoife Mooney; Deirdre Leavy; Katie Ridge; Jamie Sugrue; Mubarak Aldoseri; Jo Hannah Kelliher; Martina Hennessy; Declan Byrne; Paul Browne; Christopher L Bacon; Catriona Doyle; Ruth O'Riordan; Anne-Marie McLaughlin; Ciaran Bannan; Ignacio Martin-Loeches; Arthur White; Rachel M McLoughlin; Colm Bergin; Nollaig M Bourke; Cliona O'Farrelly; Niall Conlon; Clíona Ní Cheallaigh
Journal:  Heliyon       Date:  2022-04-01

Review 5.  Circulating biomarkers of inflammaging as potential predictors of COVID-19 severe outcomes.

Authors:  Jacopo Sabbatinelli; Giulia Matacchione; Angelica Giuliani; Deborah Ramini; Maria Rita Rippo; Antonio Domenico Procopio; Massimiliano Bonafè; Fabiola Olivieri
Journal:  Mech Ageing Dev       Date:  2022-03-25       Impact factor: 5.498

6.  Neutrophil and Eosinophil Responses Remain Abnormal for Several Months in Primary Care Patients With COVID-19 Disease.

Authors:  B N Jukema; K Smit; M T E Hopman; C C W G Bongers; T C Pelgrim; M H Rijk; T N Platteel; R P Venekamp; D L M Zwart; F H Rutten; L Koenderman
Journal:  Front Allergy       Date:  2022-07-27

7.  The Systemic Immune Response in COVID-19 Is Associated with a Shift to Formyl-Peptide Unresponsive Eosinophils.

Authors:  Leo Koenderman; Maarten J Siemers; Corneli van Aalst; Suzanne H Bongers; Roy Spijkerman; Bas J J Bindels; Giulio Giustarini; Harriët M R van Goor; Karin A H Kaasjager; Nienke Vrisekoop
Journal:  Cells       Date:  2021-05-05       Impact factor: 6.600

8.  Kinetics of Neutrophil Subsets in Acute, Subacute, and Chronic Inflammation.

Authors:  Suzanne H Bongers; Na Chen; Erinke van Grinsven; Selma van Staveren; Marwan Hassani; Roy Spijkerman; Lilian Hesselink; Adèle T Lo Tam Loi; Corneli van Aalst; Guus P Leijte; Matthijs Kox; Peter Pickkers; Falco Hietbrink; Luke P H Leenen; Leo Koenderman; Nienke Vrisekoop
Journal:  Front Immunol       Date:  2021-06-24       Impact factor: 7.561

  8 in total

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