ArticleFrontiers in immunology2026
Peripheral blood B-cell compartment dysregulation in multidrug-resistant tuberculosis is associated with reduced circulating marginal zone-like B cells.
Article 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.
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
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Multidrug-resistant tuberculosis (MDR-TB) remains a major global health challenge. While T cell-mediated immunity in tuberculosis is well characterized, alterations in circulating B-cell subsets during chronic MDR-TB are less well defined. Methods: Peripheral blood mononuclear cells (PBMCs) from healthy controls [interferon gamma release assay negative (IGRA Results: Frequencies of major T-cell and natural killer (NK)-cell populations were broadly similar across groups. In contrast, patients with ATB showed a reduction in total CD19 Conclusion: MDR-TB is associated with broad perturbations of the peripheral B-cell compartment, including reduced ASCs and decreased circulating MZ B cells. These findings highlight B-cell dysregulation as a feature of active disease and identify MZ B cells as a subset of interest for further investigation rather than as a stand-alone diagnostic marker.
Indexed as
Identifiers
What Socratic holds
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 Socratic graph.