TY - JOUR
T1 - Stratification of hospitalized COVID-19 patients into clinical severity progression groups by immuno-phenotyping and machine learning
AU - Mueller, Yvonne M.
AU - Schrama, Thijs J.
AU - Ruijten, Rik
AU - Schreurs, Marco W.J.
AU - Grashof, Dwin G.B.
AU - van de Werken, Harmen J.G.
AU - Lasinio, Giovanna Jona
AU - Álvarez-Sierra, Daniel
AU - Kiernan, Caoimhe H.
AU - Castro Eiro, Melisa D.
AU - van Meurs, Marjan
AU - Brouwers-Haspels, Inge
AU - Zhao, Manzhi
AU - Li, Ling
AU - de Wit, Harm
AU - Ouzounis, Christos A.
AU - Wilmsen, Merel E.P.
AU - Alofs, Tessa M.
AU - Laport, Danique A.
AU - van Wees, Tamara
AU - Kraker, Geoffrey
AU - Jaimes, Maria C.
AU - Van Bockstael, Sebastiaan
AU - Hernández-González, Manuel
AU - Rokx, Casper
AU - Rijnders, Bart J.A.
AU - Pujol-Borrell, Ricardo
AU - Katsikis, Peter D.
N1 - © 2022. The Author(s).
PY - 2022/2/17
Y1 - 2022/2/17
N2 - Quantitative or qualitative differences in immunity may drive clinical severity in COVID-19. Although longitudinal studies to record the course of immunological changes are ample, they do not necessarily predict clinical progression at the time of hospital admission. Here we show, by a machine learning approach using serum pro-inflammatory, anti-inflammatory and anti-viral cytokine and anti-SARS-CoV-2 antibody measurements as input data, that COVID-19 patients cluster into three distinct immune phenotype groups. These immune-types, determined by unsupervised hierarchical clustering that is agnostic to severity, predict clinical course. The identified immune-types do not associate with disease duration at hospital admittance, but rather reflect variations in the nature and kinetics of individual patient’s immune response. Thus, our work provides an immune-type based scheme to stratify COVID-19 patients at hospital admittance into high and low risk clinical categories with distinct cytokine and antibody profiles that may guide personalized therapy.
AB - Quantitative or qualitative differences in immunity may drive clinical severity in COVID-19. Although longitudinal studies to record the course of immunological changes are ample, they do not necessarily predict clinical progression at the time of hospital admission. Here we show, by a machine learning approach using serum pro-inflammatory, anti-inflammatory and anti-viral cytokine and anti-SARS-CoV-2 antibody measurements as input data, that COVID-19 patients cluster into three distinct immune phenotype groups. These immune-types, determined by unsupervised hierarchical clustering that is agnostic to severity, predict clinical course. The identified immune-types do not associate with disease duration at hospital admittance, but rather reflect variations in the nature and kinetics of individual patient’s immune response. Thus, our work provides an immune-type based scheme to stratify COVID-19 patients at hospital admittance into high and low risk clinical categories with distinct cytokine and antibody profiles that may guide personalized therapy.
UR - http://www.scopus.com/inward/record.url?scp=85124779656&partnerID=8YFLogxK
U2 - 10.1038/s41467-022-28621-0
DO - 10.1038/s41467-022-28621-0
M3 - Article
C2 - 35177626
AN - SCOPUS:85124779656
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 915
ER -