ReviewImmunological reviews2026
Sex as a Biological Variable in Tuberculosis Pathogenesis.
Review in Immunological reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Tuberculosis (TB) remains a leading cause of infectious mortality worldwide, disproportionately affecting vulnerable populations and posing significant challenges for global health. Sex profoundly influences TB susceptibility, disease progression, treatment outcomes, and drug pharmacokinetics. While biological factors such as sex hormones and, to some extent, sex chromosomes are suspected drivers, the mechanisms behind these sex-based differences remain poorly understood. Emerging evidence indicates that males experience higher TB incidence, more severe disease, and worse treatment outcomes, including higher rates of relapse, treatment failure, and death, while females often achieve better drug exposure and display stronger immune responses. Differences in adverse drug reactions and pharmacokinetics also vary greatly by sex, suggesting potential for personalized, optimized therapy. These findings raise important questions: How does sex intersect with TB pathogenesis, drug metabolism, and resistance? Could integrating sex-specific strategies improve TB management and global control efforts? Understanding these differences is crucial to unravel the hidden drivers of TB vulnerability and to develop sex-specific, tailored therapies and precision interventions.
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Registered trials
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