Immunological sub-phenotypes and response to Convalescent Plasma in COVID-19 induced ARDS: a secondary analysis of the CONFIDENT trial.

Author:

Misset Benoit1ORCID,Diep Anh Nguyet2,Bertrand Axelle3,Piagnerelli Michael4,Hoste Eric5,Michaux Isabelle6,De Waele Elisabeth7,Dumoulin Alexander8,Jorens Philippe G9,Hauwaert Emmanuel van der10,Vallot Frédéric11,Swinnen Walter12,De Schryver Nicolas13,de Mey Nathalie14,Layios Nathalie3,Mesland Jean-Baptiste15,Robinet Sébastien3,Cavalier Etienne16,Donneau Anne-Françoise16,Moutschen Michel1,Laterre Pierre-François17

Affiliation:

1. CHU de Liège: Centre hospitalier universitaire de Liege

2. Liege University: Universite de Liege

3. University Hospital of Liège General Intensive Care Medicine: CHU de Liege Soins intensifs generaux

4. CHU de Charleroi: Centre hospitalier universitaire de Charleroi

5. UZ Gent: Universitair Ziekenhuis Gent

6. CHU UCL Namur

7. Vrije Universiteit Brussel

8. Stedelijk Ziekenhuis Roeselare: AZ Delta vzw

9. University Hospital Antwerp: Universitair Ziekenhuis Antwerpen

10. Imeldaziekenhuis: Imelda vzw

11. CHwapi: Centre Hospitalier de Wallonie Picarde

12. Algemeen Ziekenhuis Sint Blasius campus Dendermonde: Algemeen Ziekenhuis Sint Blasius

13. Clinique Saint Pierre

14. OLV Ziekenhuis Campus Aalst: Onze-Lieve-Vrouwziekenhuis Campus Aalst

15. University Hospital Saint-Luc: Cliniques Universitaires Saint-Luc

16. University of Liege: Universite de Liege

17. CHR Mons-Hainaut

Abstract

Abstract Background Convalescent Plasma (CP) reduced the mortality in COVID-19 induced ARDS (C-ARDS) patients treated in the CONFIDENT trial. As patients are immunologically heterogeneous, we hypothesized that clusters may differ in their treatment responses to CP. Methods We measured 20 cytokines, chemokines and cell adhesion markers using a multiplex technique at the time of inclusion in the CONFIDENT trial in patients of centers having accepted to participate in this secondary study. We performed descriptive statistics, unsupervised hierarchical cluster analysis, and examined the association between the clusters and CP effect on day-28 mortality. Results Of the 475 patients included in CONFIDENT, 391 (82%) were sampled, and 196/391 (50.1%) had been assigned to CP. We identified four sub-phenotypes representing 89 (22.8%), 178 (45.5%), 38 (9.7%), and 86 (22.0%) patients. The most contributing biomarkers in the principal component analysis were IL-1β, IL-12p70, IL-6, IFN-α, IL-17A, IFN-γ, IL-13, TFN-α, total IgG, and CXCL10. Sub-phenotype-1 displayed a lower immune response, sub-phenotype-2 a higher adaptive response, subphenotype-3 the highest innate antiviral, pro and anti-inflammatory response, and adhesion molecule activation, and sub-phenotype-4 a higher pro and anti-inflammatory response, migration protein and adhesion molecule activation. Sub-phenotype-2 and sub-phenotype-4 had higher severity at the time of inclusion. The effect of CP treatment on mortality appeared higher than standard care in each sub-phenotype, without heterogeneity between sub-phenotypes (p = 0.97). Conclusion In patients with C-ARDS, we identified 4 sub-phenotypes based on their immune response. These sub-phenotypes were associated with different clinical profiles. The response to CP was similar across the 4 sub-phenotypes.

Publisher

Research Square Platform LLC

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