A novel blood-based assay for treatment monitoring of tuberculosis.


Journal

BMC research notes
ISSN: 1756-0500
Titre abrégé: BMC Res Notes
Pays: England
ID NLM: 101462768

Informations de publication

Date de publication:
30 Jun 2021
Historique:
received: 23 03 2021
accepted: 17 06 2021
entrez: 1 7 2021
pubmed: 2 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

A novel 3-gene host transcriptional signature (GBP5, DUSP3 and KLF2) has been validated for tuberculosis (TB) treatment monitoring using laboratory-based RNA sequencing platforms. The signature was recently translated by Cepheid into a prototype cartridge-based test that can be run on the GeneXpert instrument. In this study, we prospectively evaluated the change in the expression of the cartridge-based 3-gene signature following treatment initiation among pulmonary TB patients who were microbiologically cured at the end of treatment. The 3-gene signature expression level (TB score) changed significantly over time with respect to baseline among 31 pulmonary TB patients. The greatest increase in TB score occurred within the first month of treatment (median fold-increase in TB score: 1.08 [IQR 0.54-1.52]) and plateaued after 4 months of treatment (median TB score: 1.97 [IQR: 1.03-2.33]). The rapid and substantial increase of the TB score in the first month of treatment holds promise for the early identification of patients that respond to TB treatment. The plateau in TB score at 4 months may indicate early clearance of disease and could direct treatment to be shortened. These hypotheses need to be further explored with larger prospective treatment monitoring studies.

Identifiants

pubmed: 34193258
doi: 10.1186/s13104-021-05663-z
pii: 10.1186/s13104-021-05663-z
pmc: PMC8243580
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

247

Subventions

Organisme : Department for International Development
ID : 300341-102
Organisme : Bundesministerium für Bildung, Wissenschaft, Forschung und Technologie
ID : 2020 62 156
Organisme : NIAID NIH HHS
ID : U19 AI057229
Pays : United States
Organisme : U.S. Department of Defense
ID : W81XWH-18-1-0253
Organisme : Department of Foreign Affairs and Trade, Australian Government
ID : 70957
Organisme : NIH/NIAID
ID : 5U19AI057229
Organisme : NIH/NIAID
ID : 5R01AI125197-02
Organisme : Ministerie van Buitenlandse Zaken (NL)
ID : PDP15CH14
Organisme : NIH/NIAID
ID : 5U19AI109662-05
Organisme : U.S. Department of Defense
ID : W81XWH1910235
Organisme : Bill and Melinda Gates Foundation
ID : OPP1113682

Références

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pubmed: 31958400
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pubmed: 30978194
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pubmed: 26907218
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pubmed: 28941629

Auteurs

Alexandra J Zimmer (AJ)

Departments of Medicine and of Epidemiology, Biostatistics & Occupational Health, McGill University, Montreal, Canada.

Samuel G Schumacher (SG)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland.

Erik Södersten (E)

Cepheid AB, Solna, Sweden.

Anna Mantsoki (A)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland.

Romain Wyss (R)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland.

David H Persing (DH)

Cepheid, Sunnyvale, CA, USA.

Sara Banderby (S)

Cepheid AB, Solna, Sweden.

Linda Strömqvist Meuzelaar (L)

Cepheid AB, Solna, Sweden.

Jacqueline Prieto (J)

Cepheid AB, Solna, Sweden.

Devasena Gnanashanmugam (D)

Cepheid, Sunnyvale, CA, USA.

Purvesh Khatri (P)

Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Department of Medicine, Center for Biomedical Informatics Research, Stanford University School of Medicine, Stanford, CA, 94305, USA.

Stefano Ongarello (S)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland.

Morten Ruhwald (M)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland. Morten.Ruhwald@finddx.org.

Claudia M Denkinger (CM)

FIND, Chemin des Mines 9, Geneva, 1202, Switzerland.
Division of Tropical Medicine, Center for Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.

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Classifications MeSH