Clinical severity classes in COVID-19 pneumonia have distinct immunological profiles, facilitating risk stratification by machine learning.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 23 03 2023
accepted: 25 07 2023
medline: 22 9 2023
pubmed: 21 9 2023
entrez: 21 9 2023
Statut: epublish

Résumé

Clinical triage in coronavirus disease 2019 (COVID-19) places a heavy burden on senior clinicians during a pandemic situation. However, risk stratification based on serum biomarker bioprofiling could be implemented by a larger, nonspecialist workforce. Measures of Complement Activation and inflammation in patientS with CoronAvirus DisEase 2019 (CASCADE) patients ( The LDA models distinctly discriminated between deteriorators, nondeteriorators, and HC, with IL-27, IP-10, MDC, ferritin, C5, and sC5b-9 among the key predictor variables during deterioration. C3a and C5 were elevated in all severity classes vs. HC ( Distinct immunological fingerprints from serum biomarkers exist within different severity classes of COVID-19, and harnessing them using machine learning enabled the development of clinically useful triage and prognostic tools. Complement-mediated lung injury plays a key role in COVID-19 pneumonia, and preliminary results hint at the usefulness of a C5 inhibitor in COVID-19 recovery.

Identifiants

pubmed: 37731491
doi: 10.3389/fimmu.2023.1192765
pmc: PMC10508987
doi:

Substances chimiques

Interleukin-27 0
Immunosuppressive Agents 0

Banques de données

ClinicalTrials.gov
['NCT04453527']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1192765

Informations de copyright

Copyright © 2023 Wiffen, D’Cruz, Brown, Higenbottam, Bernstein, Campbell, Moellman, Ghosh, Richardson, Weston-Davies and Chauhan.

Déclaration de conflit d'intérêts

Authors TH, CR, and WW-D are employed by AKARI Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Laura Wiffen (L)

Research and Innovation Department, Portsmouth Hospitals University National Health Service (NHS) Trust, Portsmouth, United Kingdom.

Leon Gerard D'Cruz (LG)

Research and Innovation Department, Portsmouth Hospitals University National Health Service (NHS) Trust, Portsmouth, United Kingdom.
School of Pharmacy & Biomedical Science, University of Portsmouth, Portsmouth, United Kingdom.

Thomas Brown (T)

Research and Innovation Department, Portsmouth Hospitals University National Health Service (NHS) Trust, Portsmouth, United Kingdom.

Tim W Higenbottam (TW)

AKARI Therapeutics PLC, London, United Kingdom.

Jonathan A Bernstein (JA)

Department of Internal Medicine, Division of Rheumatology, Allergy and Immunology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Courtney Campbell (C)

Ohio State University Medical Centre, Department of Cardiovascular Medicine, Columbus, OH, United States.

Joseph Moellman (J)

Department of Emergency Medicine, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Debajyoti Ghosh (D)

Department of Internal Medicine, Division of Rheumatology, Allergy and Immunology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Clive Richardson (C)

AKARI Therapeutics PLC, London, United Kingdom.

Wynne Weston-Davies (W)

AKARI Therapeutics PLC, London, United Kingdom.

Anoop J Chauhan (AJ)

Research and Innovation Department, Portsmouth Hospitals University National Health Service (NHS) Trust, Portsmouth, United Kingdom.
School of Pharmacy & Biomedical Science, University of Portsmouth, Portsmouth, United Kingdom.

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