Benchmarking transcriptional host response signatures for infection diagnosis.

aging bacteria cross-reactivity data compendium infection diagnosis influenza signature non-infectious conditions robustness signature evaluation framework transcriptional host response signature virus

Journal

Cell systems
ISSN: 2405-4720
Titre abrégé: Cell Syst
Pays: United States
ID NLM: 101656080

Informations de publication

Date de publication:
21 12 2022
Historique:
received: 18 03 2022
revised: 04 08 2022
accepted: 22 11 2022
entrez: 22 12 2022
pubmed: 23 12 2022
medline: 27 12 2022
Statut: ppublish

Résumé

Identification of host transcriptional response signatures has emerged as a new paradigm for infection diagnosis. For clinical applications, signatures must robustly detect the pathogen of interest without cross-reacting with unintended conditions. To evaluate the performance of infectious disease signatures, we developed a framework that includes a compendium of 17,105 transcriptional profiles capturing infectious and non-infectious conditions and a standardized methodology to assess robustness and cross-reactivity. Applied to 30 published signatures of infection, the analysis showed that signatures were generally robust in detecting viral and bacterial infections in independent data. Asymptomatic and chronic infections were also detectable, albeit with decreased performance. However, many signatures were cross-reactive with unintended infections and aging. In general, we found robustness and cross-reactivity to be conflicting objectives, and we identified signature properties associated with this trade-off. The data compendium and evaluation framework developed here provide a foundation for the development of signatures for clinical application. A record of this paper's transparent peer review process is included in the supplemental information.

Identifiants

pubmed: 36549274
pii: S2405-4712(22)00466-5
doi: 10.1016/j.cels.2022.11.007
pmc: PMC9768893
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

974-988.e7

Commentaires et corrections

Type : CommentOn

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests Icahn School of Medicine at Mount Sinai has submitted a provisional patent related to this work. A.C., D.G.C., S.C.S., S.H.K., and E.Z. are inventors of the technology filed through ISMMS related to this manuscript. S.H.K. receives consulting fees from Peraton.

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Auteurs

Daniel G Chawla (DG)

Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06511, USA.

Antonio Cappuccio (A)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Andrea Tamminga (A)

Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06511, USA.

Stuart C Sealfon (SC)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Elena Zaslavsky (E)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: elena.zaslavsky@mssm.edu.

Steven H Kleinstein (SH)

Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06511, USA; Department of Pathology and Department of Immunobiology, Yale School of Medicine, New Haven, CT 06511, USA. Electronic address: steven.kleinstein@yale.edu.

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Classifications MeSH