Evidence map›Paper›PMID 32755620›Full record

ReviewJournal of molecular biology2021

Interleukin 35 Regulatory B Cells.

Jin Kyeong Choi, Charles E Egwuagu

Open access · greenAbstract readReview
In one paragraph

Review in Journal of molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 50 citations in OpenAlex.

  1. The TPx Protein ofCells · 2026
    Article
  2. Review
  3. The role and mechanism of IL‑35 in myasthenia gravis (Review).International journal of molecular medicine · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Advances in tumor-infiltrating B lymphocytes.Central-European journal of immunology · 2025
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. IL-35 promotes IL-35Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  19. Review
  20. Review
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

2 authors at 2 institutions in 2 countries.

Jin Kyeong ChoiMolecular Immunology Section, Laboratory of Immunology, National Eye Institute (NEI), National Institutes of Health, Bethesda, MD 20892-1857, USA; Department of Immunology, Jeonbuk National University Medical School, Jeonju, Jeonbuk 54896, Republic of Korea.
Charles E EgwuaguMolecular Immunology Section, Laboratory of Immunology, National Eye Institute (NEI), National Institutes of Health, Bethesda, MD 20892-1857, USA. Electronic address: egwuaguc@nei.nih.gov.
National Eye Institute · USNational Institutes of Health · US

Funding

Development of Immunologic therapies against uveitisZIAEY000350 · NEI · NATIONAL EYE INSTITUTE · PI EGWUAGU, CHARLES E · 2009 to 2025
$6.7M
Mechanisms of immune homeostasis and regulation of intraocular inflammationZIAEY000372 · NEI · NATIONAL EYE INSTITUTE · PI EGWUAGU, CHARLES E · 2009 to 2025
$6.5M
Role of IL-12 family cytokines in human autoimmune UveitisZIAEY000262 · NEI · NATIONAL EYE INSTITUTE · PI EGWUAGU, CHARLES E · 2009 to 2025
$5.9M
Regulation of JAK/STAT pathways in the eyeZIAEY000315 · NEI · NATIONAL EYE INSTITUTE · PI EGWUAGU, CHARLES E · 2009 to 2025
$5.4M
Intramural NIH HHS ZIA EY000350
6 · The paper itself

Abstract

B lymphocytes play a central role in host immunity. They orchestrate humoral immune responses that modulate activities of other immune cells and produce neutralizing antibodies that confer lasting immunity to infectious diseases including smallpox, measles and poliomyelitis. In addition to these traditional functions is the recent recognition that B cells also play critical role in maintaining peripheral tolerance and suppressing the development or severity of autoimmune diseases. Their immune suppressive function is attributed to relatively rare populations of regulatory B cells (Bregs) that produce anti-inflammatory cytokines including interleukin 10 (IL-10), IL-35 and transforming growth factor-β. The IL-35-producing B cell (i35-Breg) is the newest Breg subset described. i35-Bregs suppress central nervous system autoimmune diseases by inducing infectious tolerance whereby conventional B cells acquire regulatory functions that suppress pathogenic Th17 responses. In this review, we discuss immunobiology of i35-Breg cell, i35-Breg therapies for autoimmune diseases and potential therapeutic strategies for depleting i35-Bregs that suppress immune responses against pathogens and tumor cells.

Indexed as

AnimalsB-Lymphocytes, RegulatoryB-Lymphocyte SubsetsCell PlasticityCytokinesDisease ManagementDisease SusceptibilityHumansImmune System DiseasesImmunomodulationImmunotherapyInterleukinsSignal TransductionT-LymphocytesCytokinesinterleukin-35, humanInterleukinsBreg immunotherapyinterleukin 10interleukin 35interleukin-35-producing Breg (i35-Breg)regulatory B cell (Breg)

Identifiers

PMID32755620
PMCPMC7779660
OpenAlexW3046688476

What OpenQuestion holds

Textmetadata
LicenceTDM
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.