Evidence map›Paper›PMID 26254185›Full record

ReviewInternational immunology2015

Regulatory B10 cell development and function.

Jacquelyn M Lykken, Kathleen M Candando, Thomas F Tedder

Open access · bronzeAbstract readReview
In one paragraph

Review in International immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

72 citing papers in PubMed, 128 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Single-cell atlas of grass carp (Zoological research · 2025
    Article
  5. Article
  6. Review
  7. Advances in tumor-infiltrating B lymphocytes.Central-European journal of immunology · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Influence of Housing Temperature and Genetic Diversity on Allogeneic T Cell-Induced Tissue Damage in Mice.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Article
  13. TLR9 Signaling Is Required for theInternational journal of molecular sciences · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Update on B Cell Response in Periodontitis.Advances in experimental medicine and biology · 2022
    Article

12 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Jacquelyn M LykkenDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Kathleen M CandandoDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Thomas F TedderDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA thomas.tedder@duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

Basic Immunology Training ProgramT32AI052077 · NIAID · DUKE UNIVERSITY · PI KRANGEL, MICHAEL S · 2002 to 2024
$4.2M
NIAID NIH HHS T32 AI052077
6 · The paper itself

Abstract

B cells are known to instigate and promulgate immune responses by producing antibodies and presenting antigens to T cells. However, a rare but potent B-cell subset in both humans and mice is capable of inhibiting immune responses through the production of the anti-inflammatory cytokine IL-10. Regulatory B cells do not express any unique combination of surface markers but instead represent a small population of B cells that have acquired the unique ability to produce IL-10. This numerically rare B-cell subset is therefore functionally referred to as 'B10 cells' to reflect both their molecular program and the fact that their anti-inflammatory effects in models of autoimmunity, infection and cancer are solely attributable to IL-10 production. As with most B cells, B10 cell development and function appear to be predominantly, if not exclusively, driven by antigen-receptor signals. Once generated, B10 cells respond to both innate and adaptive immune signals, with a requirement for antigen-specific local interactions with T cells to induce IL-10 production and to provide optimal immune suppression in mouse models of autoimmune disease. B10 cells therefore provide an antigen-specific mechanism for delivering IL-10 locally to sites of immune activation and inflammation. The ability of B10 cells to regulate innate and adaptive immune responses makes them an ideal therapeutic target for the treatment of many immune-related disorders.

Indexed as

Antigen PresentationImmunity, HumoralAnimalsB-Lymphocytes, RegulatoryCell CommunicationDermatitis, ContactDisease Models, AnimalGene Expression RegulationHumansImmunity, InnateInterleukin-10MiceReceptors, Antigen, B-CellSignal TransductionSpleenT-LymphocytesIL10 protein, humanInterleukin-10Receptors, Antigen, B-Cellantigen specificityB10 cellB lymphocyteIL-10regulatory B cell

Identifiers

PMID26254185
PMCPMC4817073
OpenAlexW2158431089

What OpenQuestion holds

Textmetadata
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.