Diagnosis of infectious diseases in immunocompromised hosts using metagenomic next generation sequencing-based diagnostics.

Diagnostics Genome Immunocompromised Infection surveillance Infectious diseases Liquid biopsy Metagenomic next generation sequencing Pathogens

Journal

Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558

Informations de publication

Date de publication:
05 2022
Historique:
received: 01 07 2021
revised: 28 10 2021
accepted: 01 11 2021
pubmed: 23 11 2021
medline: 20 4 2022
entrez: 22 11 2021
Statut: ppublish

Résumé

The diagnosis of infectious diseases in immunocompromised hosts presents unique challenges for the clinician. Metagenomic next generation sequencing (mNGS) based diagnostics that identify microbial nucleic acids in clinical samples (mNGS for pathogen identification or mNGSpi) may be a useful tool in addressing some of these challenges. Studies of mNGSpi in immunocompromised hosts have demonstrated that these diagnostics are capable of identifying causative organisms in a subset of patients for whom conventional testing has been negative. While these studies provide proof of concept for mNGSpi utility, they have a number of limitations, which make it difficult to confidently assess test performance and clinical impact based on current data. Future studies will likely feature larger cohort sizes and controlled interventional study designs that assess the impact of mNGSpi on clinical endpoints. They will also likely include assessments of the clinical value of data generated by mNGS beyond pathogen identification.

Identifiants

pubmed: 34802773
pii: S0268-960X(21)00112-0
doi: 10.1016/j.blre.2021.100906
pii:
doi:

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

100906

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI118690
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Amanda M Casto (AM)

Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, United States of America; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America. Electronic address: amcasto@uw.edu.

David N Fredricks (DN)

Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, United States of America; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America. Electronic address: dfredric@fredhutch.org.

Joshua A Hill (JA)

Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, WA, United States of America; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America. Electronic address: jahill3@fredhutch.org.

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Classifications MeSH