Evidence map›Paper›PMID 35749397›Full record

ArticlePloS one2022

Serial T-SPOT.TB responses in Tanzanian adolescents: Transient, persistent and irregular conversions.

Maryam A Amour, Christiaan A Rees, Patricia J Munseri, Jamila Said, Albert K Magohe, Mecky Matee, Elizabeth A Talbot, Robert D Arbeit, Kisali Pallangyo, C Fordham von Reyn

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 14% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 17 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Maryam A AmourMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.ORCID 0000-0002-2590-2516
Christiaan A ReesGeisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States of America.
Patricia J MunseriMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Jamila SaidMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Albert K MagoheMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Mecky MateeMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Elizabeth A TalbotGeisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States of America.
Robert D ArbeitTufts University School of Medicine, Boston, Massachusetts, United States of America.
Kisali PallangyoMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
C Fordham von ReynGeisel School of Medicine at Dartmouth, Hanover, New Hampshire, United States of America.
Muhimbili University of Health and Allied Sciences · TZDartmouth College · USTufts University · US

Funding

Tuberculosis Research Institute at MUHASD43TW009573 · FIC · DARTMOUTH COLLEGE · PI ADAMS, LISA VIRGINIA · 2013 to 2022
$3.0M
FIC NIH HHS D43 TW009573
6 · The paper itself

Abstract

backgroundProspective studies of interferon-gamma release assays (IGRA) on healthy subjects in tuberculosis-endemic regions have not examined the long-term variability of serial assays. This issue is relevant to the interpretation of tuberculosis (TB) vaccine trials based on prevention of infection.

methodsT-SPOT.TB assays were performed manually on healthy adolescents during a tuberculosis vaccine trial in Tanzania at 5 intervals over 3 years. Assay results were defined as negative, positive, borderline or invalid. Subsequently, microtiter plates were analyzed by an automated reader to obtain quantitative counts of spot forming cells (SFCs) for the present analysis.

results3387 T-SPOT.TB samples were analyzed from 928 adolescents; manual and automated assay results were 97% concordant. Based on the quantitative results 143 (15%) participants were prevalent IGRA-positives at baseline, were ineligible for further study. Among the remaining IGRA-negative participants, the annual rate of IGRA conversion was 2·9%. Among 43 IGRA converters with repeat assays 12 (28%) were persistent converters, 16 (37%) were transient converters, and 15 (35%) comprised a new category defined as irregular converters (≥2 different subsequent results). ESAT-6 and CFP-10 responses were higher in prevalent than incident positives: 53 vs 36 for CFP-10 (p < 0·007); 44 vs 34 for ESAT-6 (p = 0·12).

conclusionsDefinitions of IGRA conversion, reversion, and persistence depend critically on the frequency of testing. Multiple shifts in categories among adolescents in a TB-endemic country may represent multiple infections, variable host responses in subclinical infection, or assay variation. These findings should to be considered in the design and interpretation of TB vaccine trials based on prevention of infection. Household contact studies could determine whether even transient IGRA conversion might represent exposure to an active case of M. tuberculosis disease.

Indexed as

Mycobacterium tuberculosisTuberculosisTuberculosis VaccinesAdolescentHumansInterferon-gamma Release TestsProspective StudiesTanzaniaTuberculin TestTuberculosis Vaccines

Identifiers

PMID35749397
PMCPMC9231806
OpenAlexW4283399277

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.