Evidence map›Paper›PMID 40455886›Full record

Observational studyThe Journal of infectious diseases2025

Impact of Puberty on Immune Responses to Mycobacterium tuberculosis in South African Adolescents.

Léanie Kleynhans, Elizna Maasdorp, Candice I Snyders, James A Seddon

Abstract readObservational Study
In one paragraph

Observational study in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

4 authors.

Léanie KleynhansDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID 0000-0003-1635-253X
Elizna MaasdorpDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for TB Research, Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID 0000-0002-3402-169X
Candice I SnydersDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, Division of Immunology, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
James A SeddonDesmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID 0000-0002-2296-2302

Funding

UK Department for International Development MR/R007942/1UK Medical Research Council
6 · The paper itself

Abstract

backgroundAs individuals progress through adolescence, their risk of tuberculosis (TB) increases, and the type of disease that develops changes, with increasing cavitary formation and parenchymal tissue destruction. While it is widely assumed that the changes in risk and disease phenotype are due to puberty exerting an impact on host immune responses to Mycobacterium tuberculosis, this relationship has been poorly studied.

methodsTeen TB was an observational study that recruited 50 adolescents with pulmonary TB and 50 controls exposed to TB in Cape Town, South Africa. Blood was collected at baseline and again at month 2 from those with TB. Concentrations of 43 cytokines and 19 hormones were measured and compared between individuals with TB and controls, and changes were monitored over time in those with TB. The relationship between Tanner stage and cytokine/endocrine concentrations was also assessed.

resultsIL-1ra, IP-10, SAP, cortisol, lipocalin 2, and resistin were higher, while ghrelin, T3, and DHEAS were lower, in adolescents with TB vs healthy controls. DHEAS, progesterone, luteinizing hormone, testosterone, C peptide, estradiol, and cortisol were positively correlated and T3 negatively correlated with Tanner stage in healthy controls. In adolescents with TB, there was no association between Tanner stage and cytokine/endocrine markers.

conclusionsWhile in healthy individuals there was a strong association between Tanner stage and endocrine markers, this relationship was absent in adolescents with TB. TB disease appears to disrupt the normal physiologic process of puberty. This could have a substantial impact on growth and development for adolescents developing TB during this critical time.

Indexed as

Mycobacterium tuberculosisPubertyTuberculosisTuberculosis, PulmonaryAdolescentChildCytokinesFemaleHumansMaleSouth AfricaCytokinesadolescentsendocrineimmuneTanner stagetuberculosis

Identifiers

PMID40455886
PMCPMC12349956

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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.