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.

Stratification of hospitalized COVID-19 patients into clinical severity progression groups by immuno-phenotyping and machine learning / Mueller, Yvonne M.; Schrama, Thijs J.; Ruijten, Rik; Schreurs, Marco W. J.; Grashof, Dwin G. B.; van de Werken, Harmen J. G.; JONA LASINIO, Giovanna; Álvarez-Sierra, Daniel; Kiernan, Caoimhe H.; Castro Eiro, Melisa D.; van Meurs, Marjan; Brouwers-Haspels, Inge; Zhao, Manzhi; Li, Ling; de Wit, Harm; Ouzounis, Christos A.; Wilmsen, Merel E. P.; Alofs, Tessa M.; Laport, Danique A.; van Wees, Tamara; Kraker, Geoffrey; Jaimes, Maria C.; Van Bockstael, Sebastiaan; Hernández-González, Manuel; Rokx, Casper; Rijnders, Bart J. A.; Pujol-Borrell, Ricardo; Katsikis, Peter D.. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - (2022), pp. 1-13. [10.1038/s41467-022-28621-0]

Stratification of hospitalized COVID-19 patients into clinical severity progression groups by immuno-phenotyping and machine learning

Giovanna Jona Lasinio
Membro del Collaboration Group
;
2022

Abstract

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.
2022
machine learning; multinomial regression; immuno-type; covid-19
01 Pubblicazione su rivista::01a Articolo in rivista
Stratification of hospitalized COVID-19 patients into clinical severity progression groups by immuno-phenotyping and machine learning / Mueller, Yvonne M.; Schrama, Thijs J.; Ruijten, Rik; Schreurs, Marco W. J.; Grashof, Dwin G. B.; van de Werken, Harmen J. G.; JONA LASINIO, Giovanna; Álvarez-Sierra, Daniel; Kiernan, Caoimhe H.; Castro Eiro, Melisa D.; van Meurs, Marjan; Brouwers-Haspels, Inge; Zhao, Manzhi; Li, Ling; de Wit, Harm; Ouzounis, Christos A.; Wilmsen, Merel E. P.; Alofs, Tessa M.; Laport, Danique A.; van Wees, Tamara; Kraker, Geoffrey; Jaimes, Maria C.; Van Bockstael, Sebastiaan; Hernández-González, Manuel; Rokx, Casper; Rijnders, Bart J. A.; Pujol-Borrell, Ricardo; Katsikis, Peter D.. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - (2022), pp. 1-13. [10.1038/s41467-022-28621-0]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1612057
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