Evidence map›Paper›PMID 42500121›Full record

ArticleOpen forum infectious diseases2026

Associations Between QuantiFERON-TB Gold Plus IFNγ Concentrations and Progression to Symptomatic Tuberculosis in Global High-Burden TB Settings.

Justine Sunshine, Michael Shaffer, Linda L Han, Deepali Gaikwad, Amelia A Houana, Maria Tarcela Gler, Sri Rezeki Hadinegoro, Willem A Hanekom, Javier R Lama, Monde Muyoyeta and 14 more

Registry-linked trialAbstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05190146 (A Multi-country, Epidemiologic Study to Assess the Interferon Gamma Release Assay), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05190146 completednot on this map

A Multi-country, Epidemiologic Study to Assess the Interferon Gamma Release Assay (IGRA) Positivity, and to Build Capacity to Conduct a Tuberculosis (TB) Vaccine Efficacy Study, in Populations With a High TB Disease Burden

TypeobservationalSponsorGates Medical Research InstituteRan2021 to 2024Enrolled7,203ConditionsTuberculosis, Pulmonary
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Justine SunshineClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Michael ShafferClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Linda L HanClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Deepali GaikwadDepartment of Pulmonary Medicine, PCMC'S PGI YCM Hospital, Pune, Maharashtra, India.
Amelia A HouanaCentro de Investigação em Saúde de Manhiça (CISM), Maputo, Mozambique.ORCID https://orcid.org/0009-0004-9524-4995
Maria Tarcela GlerTB HIV Innovations and Clinical Research Foundation, Cavite, Philippines.
Sri Rezeki HadinegoroDepartment of Child Health Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Willem A HanekomAfrica Health Research Institute, KwaZulu-Natal, South Africa.
Javier R LamaAsociación Civil Impacta Salud y Educación, Lima, Peru.ORCID https://orcid.org/0000-0002-4983-5725
Monde MuyoyetaCentre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia.ORCID https://orcid.org/0000-0003-3609-5403
Sissy MusalaNational Tuberculosis Program/National TB Reference Laboratory', Kinshasa City, DRC.
Videlis NdubaKenya Medical Research Institute, Centre for Respiratory Diseases Research (CRDR), Nairobi, Kenya.ORCID https://orcid.org/0000-0002-2266-8349
Valeria C RollaClinical Research Laboratory on Mycobacteria, National Institute of Infectious Diseases Evandro Chagas-Fiocruz, Rio de Janeiro, Brazil.
Tapash RoyIRD Global, Bangladesh Country Office, Dhaka, Bangladesh.
Jayne S SutherlandVaccines and Immunity Theme, Medical Research Council Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.ORCID https://orcid.org/0000-0002-7083-4997
Celso KhosaInstituto Nacional de Saúde (INS), Marracuene, Mozambique.ORCID https://orcid.org/0000-0001-6701-4202
Anne WajjaMedical Research Council, Uganda Virus Research Institute and London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Timothy M WalkerOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Amy CinarClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Alexander C SchmidtClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.ORCID https://orcid.org/0000-0002-9226-3638
Alemnew F DagnewClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Nicole FrahmClinical Development, Gates Medical Research Institute, Cambridge, Massachusetts, USA.
for TBV02-E01 Study Group
for TBV02-E01 Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Predictive biomarkers for symptomatic tuberculosis (TB) progression would transform targeted prevention efforts. Although interferon-gamma release assays (IGRAs), including QuantiFERON® TB-Gold Plus (QFT-Plus), have been studied for this purpose, systematic evaluation of the QFT-Plus TB1 and TB2 Interferon-Gamma (IFNγ) concentrations remains limited, particularly in high-burden TB settings. Methods: Baseline TB1 and TB2 IFNγ concentrations from 5246 participants (ages 15-34 years) in TB-endemic regions were analyzed in relation to subsequent TB outcomes over a median of 525 days follow-up (NCT05190146). Participants were categorized as controls (no TB), suspected TB (no microbiological confirmation), or laboratory-confirmed TB, including a subset meeting a stringent case definition (≥2 positive microbiologic tests). Associations between baseline IFNγ concentrations and progression to symptomatic TB were assessed. Results: In the full cohort (IGRA+/- participants), baseline TB2 IFNγ concentrations were significantly higher compared with controls among participants who developed suspected TB ( Conclusions: Quantitative IFNγ concentrations from QFT-Plus, particularly TB2, were associated with progression to symptomatic TB, met or exceeded WHO-recommended sensitivity and specificity thresholds for predictive biomarkers, and may support biomarker-based stratification in TB clinical research.

Indexed as

biomarkerIFNγIGRAQFT-plustuberculosis

Identifiers

PMID42500121
PMCPMC13397382

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.