Evidence map›Paper›PMID 39946288›Full record

ArticleClinical and experimental immunology2026

The role of IgA and IgG in Mycobacterium tuberculosis infection: a cross-sectional study in Ethiopia.

Rubiyat E Islam, Meaza Zewdie, Daniel Mussa, Yonas Abebe, Tom H M Ottenhoff, Kees L M C Franken, Liya Wassie, Fekadu Abebe

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Novel Multistage SubunitVaccines · 2025
    Article
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

8 authors.

Rubiyat E IslamDepartment of Community Medicine, Institute of Health and Society, University of Oslo, Oslo, Norway.ORCID 0009-0008-2891-3262
Meaza ZewdieArmauer Hansen Research Institute, Immunology Directorate, Addis Ababa, Ethiopia.
Daniel MussaArmauer Hansen Research Institute, Immunology Directorate, Addis Ababa, Ethiopia.
Yonas AbebeArmauer Hansen Research Institute, Immunology Directorate, Addis Ababa, Ethiopia.
Tom H M OttenhoffDepartment of Infectious Disease, Leiden University Medical Center, Leiden, The Netherland.
Kees L M C FrankenDepartment of Infectious Disease, Leiden University Medical Center, Leiden, The Netherland.
Liya WassieArmauer Hansen Research Institute, Immunology Directorate, Addis Ababa, Ethiopia.ORCID 0000-0002-5494-5275
Fekadu AbebeDepartment of Community Medicine, Institute of Health and Society, University of Oslo, Oslo, Norway.

Funding

Ethiopia-Emory TB Research Training ProgramD43TW009127 · FIC · EMORY UNIVERSITY · PI HENRY M BLUMBERG, Kidist Bobosha · 2013 to 2026
$3.4M
Faculty of Medicine, University of OsloFIC NIH HHS D43 TW009127Institute of Health and Society
6 · The paper itself

Abstract

introductionDespite the high global prevalence of Mycobacterium tuberculosis (Mtb) infection in humans, most infected individuals achieve a stable immunological equilibrium, without showing clinical signs and symptoms of tuberculosis (TB). Although the role of antibodies in TB is assumed to be relatively small compared with cell-mediated immunity, their role in TB has been documented in a few recent studies.

methodsIn this cross-sectional study, we quantitated antibody responses to Mtb antigens, lipoarabinomannan (LAM), and heparin-binding hemagglutinin adhesin (HBHA) by determining antigen-specific immunoglobulin A(IgA) and G(IgG) secretion levels using enzyme-linked immunosorbent assay in serum and saliva of pulmonary TB patients (PTB), their household contacts, and community controls (determined by QuantiFERON TB Gold assay QFT-test result).

resultsThe HBHA-specific IgA levels were significantly higher in both saliva and serum in household contacts groups compared with PTB patients (P = 0.013, P = 0.023). Exposed contacts, who were QFT-negative, had higher serum HBHA-specific IgA responses compared with PTB patients (P = 0.04). QFT-negative household contacts and QFT-positive community controls showed higher HBHA and lipoarabinomannan-specific IgG responses (P = 0.006, P = 0.002, P = 0.0009, P = 0.006, respectively) than PTB patients. Generally, lipoarabinomannan and HBHA-specific IgA levels were significantly higher in saliva compared with serum (P < 0.0001) in all study groups.

conclusionOverall, the observed higher levels of IgA and IgG in controls, and exposed but QFT-negative contacts suggest a correlation with, and perhaps a role for these antibodies in preventing the development of active TB. The findings highlighted the potential involvement of saliva IgA in the immune response to Mtb, underscoring the relevance of mucosal immunity in TB infection.

Indexed as

Antibodies, BacterialImmunoglobulin AImmunoglobulin GMycobacterium tuberculosisTuberculosisTuberculosis, PulmonaryAdolescentAdultAntigens, BacterialCross-Sectional StudiesEthiopiaFemaleHumansLectinsLipopolysaccharidesMaleAntibodies, BacterialAntigens, Bacterialheparin-binding hemagglutininImmunoglobulin AImmunoglobulin GLectinslipoarabinomannanLipopolysaccharidesHBHA community controlsIgAIgGLAMmucosal immunitytuberculosis

Identifiers

PMID39946288
PMCPMC13032167

What Socratic holds

Textmetadata
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 Socratic graph.