Evidence map›Paper›PMID 26409285›Full record

ReviewClinical infectious diseases : an official publication of the Infectious Diseases Society of America2015

B in TB: B Cells as Mediators of Clinically Relevant Immune Responses in Tuberculosis.

Martin Rao, Davide Valentini, Thomas Poiret, Ernest Dodoo, Shreemanta Parida, Alimuddin Zumla, Susanna Brighenti, Markus Maeurer

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
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

39 citing papers in PubMed, 79 citations in OpenAlex.

  1. CD8Nature communications · 2026
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  7. Editorial: Tuberculosis and humoral immunity.Frontiers in immunology · 2025
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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 at 3 institutions in 2 countries.

Martin RaoDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet.
Davide ValentiniDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Thomas PoiretDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet.
Ernest DodooDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet.
Shreemanta ParidaDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet.
Alimuddin ZumlaDivision of Infection and Immunity, University College London, and NIHR Biomedical Research Centre at University College Hospitals NHS Foundation Trust, United Kingdom.
Susanna BrighentiCenter for Infectious Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Markus MaeurerDivision of Therapeutic Immunology, Department of Laboratory Medicine, Karolinska Institutet Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protective role of B cells and humoral immune responses in tuberculosis infection has been regarded as inferior to cellular immunity directed to the intracellular pathogen Mycobacterium tuberculosis. However, B-cell-mediated immune responses in tuberculosis have recently been revisited in the context of B-cell physiology and antigen presentation. We discuss in this review the diverse functions of B cells in tuberculosis, with a focus on their biological and clinical relevance to progression of active disease. We also present the peptide microarray platform as a promising strategy to discover unknown antigenic targets of M. tuberculosis that could contribute to the better understanding of epitope focus of the humoral immune system against M. tuberculosis.

Indexed as

Antibodies, BacterialAntigens, BacterialB-LymphocytesCytokinesEpitopes, B-LymphocyteHumansImmunity, CellularImmunity, HumoralMycobacterium tuberculosisPeptide LibraryTuberculosisAntibodies, BacterialAntigens, BacterialCytokinesEpitopes, B-LymphocytePeptide LibraryantibodiesB cellscytokineshost-directed therapytuberculosis

Identifiers

PMID26409285
PMCPMC4583574
OpenAlexW2245094765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.