Evidence map›Paper›PMID 39346706›Full record

ReviewOxford open immunology2024

The current understanding of the phenotypic and functional properties of human regulatory B cells (Bregs).

Nawara Faiza Ahsan, Stella Lourenço, Dimitra Psyllou, Alexander Long, Sushma Shankar, Rachael Bashford-Rogers

Abstract readReview
In one paragraph

Review in Oxford open immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. CD19Breast cancer research : BCR · 2026
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  15. Tumor secretome shapes the immune landscape during cancer progression.Journal of experimental & clinical cancer research : CR · 2025
    Review
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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

6 authors.

Nawara Faiza AhsanDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
Stella LourençoKeizo Asami Institute, Federal University of Pernambuco, Recife 50740-520, Brazil.
Dimitra PsyllouDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
Alexander LongDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
Sushma ShankarNuffield Department of Surgical Sciences, University of Oxford, Oxford OX3 7DQ, United Kingdom.
Rachael Bashford-RogersDepartment of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.ORCID https://orcid.org/0000-0002-6838-0711

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cells can have a wide range of pro- and anti- inflammatory functions. A subset of B cells called regulatory B cells (Bregs) can potently suppress immune responses. Bregs have been shown to maintain immune homeostasis and modulate inflammatory responses. Bregs are an exciting cellular target across a range of diseases, including Breg induction in autoimmunity, allergy and transplantation, and Breg suppression in cancers and infection. Bregs exhibit a remarkable phenotypic heterogeneity, rendering their unequivocal identification a challenging task. The lack of a universally accepted and exclusive surface marker set for Bregs across various studies contributes to inconsistencies in their categorization. This review paper presents a comprehensive overview of the current understanding of the phenotypic and functional properties of human Bregs while addressing the persisting ambiguities and discrepancies in their characterization. Finally, the paper examines the promising therapeutic opportunities presented by Bregs as their immunomodulatory capacities have gained attention in the context of autoimmune diseases, allergic conditions, and cancer. We explore the exciting potential in harnessing Bregs as potential therapeutic agents and the avenues that remain open for the development of Breg-based treatment strategies.

Indexed as

autoimmune diseaseB cellsBregsIL-10IL-25infectionregulationTGF-B

Identifiers

PMID39346706
PMCPMC11427547

What OpenQuestion holds

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LicenceCC BY
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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.