TY - JOUR
T1 - Flow cytometric evaluation of the neutrophil compartment in COVID-19 at hospital presentation
T2 - A normal response to an abnormal situation
AU - Spijkerman, Roy
AU - Bongers, Suzanne H.
AU - Bindels, Bas J.J.
AU - Tinnevelt, Gerjen H.
AU - Giustarini, Giulio
AU - Jorritsma, Nikita K.N.
AU - Buitenwerf, Wiebe
AU - van Spengler, Daan E.J.
AU - Delemarre, Eveline M.
AU - Nierkens, Stefan
AU - van Goor, Harriët M.R.
AU - Jansen, Jeroen J.
AU - Vrisekoop, Nienke
AU - Hietbrink, Falco
AU - Leenen, Luke P.H.
AU - Kaasjager, Karin A.H.
AU - Koenderman, Leo
AU - Nijdam, Thomas M.P.
AU - van de Ven, Nils L.M.
AU - Verhaegh, Remi
AU - Spanjaard, Judith S.
AU - Verboeket, Benjamin W.
AU - Laane, Duco
AU - van Wessem, Karlijn
AU - Mulder, Eva
AU - Heijerman, Harry
AU - Zabaleta, Amely Daza
AU - van den bos, Frederiek
AU - Stiphout, Feikje
AU - Rademaker, Emma
AU - Varkila, Meri R.J.
AU - Mul, Nikki d.
AU - Cremer, Olaf L.
AU - Slooter, Arjen
AU - Limper, Maarten
AU - van Wijk, Femke
AU - Pandit, Aridaman
AU - Leavis, Helen
AU - Jukema, Bernard N.
AU - Clark, Chantal C.
AU - Barendrecht, Arjan D.
AU - Seinen, Cor W.
AU - Drost-Verhoef, Sandra
AU - Smits, Simone
AU - Parr, Naomi M.J.
AU - Sebastian, Sylvie A.E.
AU - van der Vries, Erhard
AU - Maas, Coen
AU - Haitjema, Saskia
AU - Hoefer, Imo E.
N1 - Funding Information:
The authors thank Paul van Hoof, Roelof‐Jan van der Lei, Geert Weijers, Andreas Boehmler, and Markus Kaymer from the Beckman Coulter team for technical support. The authors also thank Dr. S. Rao for critically reading and editing the manuscript. This article was supported by a grant (grant #400.17.604) of the Dutch Research Council (NWO) in the framework of the “Startimpulse” Dutch National Research Agenda (NWA) and by Health Holland (grant #20064).
Publisher Copyright:
©2020 Society for Leukocyte Biology
PY - 2021/1
Y1 - 2021/1
N2 - 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.
AB - 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.
KW - 2
KW - Aged
KW - Antigens, CD/blood
KW - CD10
KW - COVID-19/blood
KW - CoV‐
KW - Female
KW - Flow Cytometry
KW - Hospitals
KW - Humans
KW - Inflammation/blood
KW - Male
KW - Middle Aged
KW - Neutrophil Activation
KW - Neutrophils/immunology
KW - SARS‐
KW - SARS-CoV-2/immunology
KW - activation
KW - flow cytometry
KW - neprilysin
KW - neutrophil
KW - SARS-CoV-2
UR - http://www.scopus.com/inward/record.url?scp=85109451870&partnerID=8YFLogxK
U2 - 10.1002/JLB.5COVA0820-520RRR
DO - 10.1002/JLB.5COVA0820-520RRR
M3 - Article
C2 - 33617030
SN - 0741-5400
VL - 109
SP - 99
EP - 114
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 1
ER -