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Journal article

Updating the WHO target product profile for next-generation Mycobacterium tuberculosis drug susceptibility testing at peripheral centres

Abstract:
Non-sputum-based diagnostic tests are necessary to enable tuberculosis (TB) diagnosis and monitoring of TB treatment. This work aimed to identify which published blood transcriptomic TB signatures have the best diagnostic performance to distinguish between TB cases and other respiratory diseases (ORDs) in symptomatic adults. These signatures were also evaluated to monitor treatment in young children, to identify signatures that might indicate when treatment could be stopped. Diagnostic performance of signatures was evaluated in adults presenting for care with symptoms associated with TB, who were recruited from primary healthcare clinics in six African countries. To identify signatures that can monitor treatment response, the same set of signatures was evaluated in young children randomised to 4- or 6-month TB treatment in the SHINE trial. Twenty transcriptomic signatures were selected and measured in whole blood using multiplex, microfluidic RT-qPCR. In the adult diagnostic cohort, nine signatures achieved equivalent performance for differentiating patients with ORDs from all TB cases. Factors associated with signature scores included HIV and country. With sensitivity benchmarked at 90%, these nine signatures achieved specificities between 44%-54%. In pooled analyses, none of the signatures met the minimal target product profile criteria for a TB triage test. Country-specific analyses, however, showed that several signatures met the minimal criteria in some countries. In children from the SHINE trial, baseline scores for all signatures were highest in children with confirmed, relative to unconfirmed and unlikely TB. Baseline scores were also higher among children with disease classified as more severe on chest x-ray. Scores declined progressively during TB treatment in the confirmed and unconfirmed TB groups; no changes in scores were observed for most signatures in the unlikely TB group. Scores were higher at the end of treatment in the 4-month than the 6-month treatment arm in the confirmed TB group; no differences were observed between treatment arms in the unconfirmed and unlikely groups. These results suggest that host blood transcriptomic signatures have potential to monitor TB treatment response in children. This work supports further development of transcriptomic signatures as TB triage tests and treatment monitoring tools
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1371/journal.pgph.0001754

Authors

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Role:
Author
ORCID:
0000-0003-4610-2427
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Role:
Author
ORCID:
0000-0002-6934-0586
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Role:
Author
ORCID:
0000-0003-3386-377X
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-0421-9264


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Funder identifier:
10.13039/100010269
Grant:
214560/Z/18/Z
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Funder identifier:
10.13039/100000200
Grant:
Grant Recipient: WHO Global TB Programme and the New Diagnostics Working Group of the Stop TB Partnership


Publisher:
Public Library of Science
Journal:
PLOS Global Public Health More from this journal
Volume:
3
Issue:
3
Pages:
e0001754-e0001754
Publication date:
2023-03-31
DOI:
EISSN:
2767-3375
ISSN:
2767-3375


Language:
English
Keywords:
Pubs id:
1335492
Local pid:
pubs:1335492
Source identifiers:
W4362468416
Deposit date:
2026-05-05
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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