Evidence mapPaperPMID 42112381Full record

SynthesisFrontiers in immunology2026

Immune dysregulation in tuberculosis-diabetes comorbidity: mechanistic and translational insights.

Aminat Y Saula, Muge Cevik, Jacqueline M Cliff, Katharina Ronacher, Ruth Bowness

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in immunology, 2026. 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

5 authors.

Aminat Y Saula *Centre for Mathematical Biology, Department of Mathematical Sciences, University of Bath, Claverton Down, Bath, United Kingdom.
Muge Cevik *Division of Infection and Global Health Research, School of Medicine, University of St Andrews, St Andrews, Scotland, United Kingdom.
Jacqueline M CliffCentre of Inflammation Research and Translational Medicine, and Department of Biosciences, Brunel University of London, London, United Kingdom.
Katharina RonacherTranslational Research Institute, Mater Research Institute, The University of Queensland, Brisbane, QLD, Australia.
Ruth BownessCentre for Mathematical Biology, Department of Mathematical Sciences, University of Bath, Claverton Down, Bath, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tuberculosis (TB) remains a leading cause of infectious disease mortality worldwide, and the rising prevalence of diabetes mellitus (DM) represents a major obstacle to TB control. DM increases susceptibility to TB, worsens disease severity, delays treatment response, and is associated with poorer outcomes, largely through disruption of host immunity. Methods: We conducted a systematic review of studies published between 1974 and May 31, 2023 that examined immunological mechanisms through which DM alters TB pathogenesis. In total, 81 eligible studies involving animal models, human participants, or combined approaches were identified and synthesised across different stages of TB. Results: Across studies, DM was associated with broad dysregulation of innate and adaptive immune responses, altered cytokine signalling, impaired granuloma structure and function, and reduced control of Conclusion: Our findings highlight DM as a key immunometabolic modifier of TB pathogenesis. They also suggest that earlier metabolic optimisation and host-directed therapeutic strategies could be explored as potential approaches to improve outcomes in this growing high-risk TB-DM population. Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42023431040.

Indexed as

Diabetes ComplicationsDiabetes MellitusMycobacterium tuberculosisTuberculosisAdaptive ImmunityAnimalsComorbidityDisease SusceptibilityHumansImmunity, Innatecomorbiditydiabetes mellitusimmune dysregulationimmune responseimmunitytuberculosis

Identifiers

PMID42112381
PMCPMC13149154

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.