Evidence map›Paper›PMID 26339791›Full record

ReviewEuropean journal of immunology2015

Perspectives on fetal derived CD5+ B1 B cells.

Richard R Hardy, Kyoko Hayakawa

Open access · bronzeAbstract readReview
In one paragraph

Review in European journal of immunology, 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
2.4field-weighted citation impact, top 12% 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, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. Induction of immune tolerance in NMOSD and MOGAD.Therapeutic advances in neurological disorders · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. CD5-Positive B Lymphocytes after Kidney Transplantation.Diagnostics (Basel, Switzerland) · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Homeostasis and regulation of autoreactive B cells.Cellular & molecular immunology · 2020
    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 1 institution in 1 country.

Richard R HardyFox Chase Cancer Center, Philadelphia, PA, USA.
Kyoko HayakawaFox Chase Cancer Center, Philadelphia, PA, USA.
Fox Chase Cancer Center · US

Funding

LY-1 B CELLS--LINEAGE DETERMINATION/ANTIBODY REPERTOIRER01AI026782 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI HARDY, RICHARD R · 1990 to 2011
$5.5M
Development and Function of Natural Autoreactive B CellsR01AI049335 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI HAYAKAWA, KYOKO · 2002 to 2012
$4.1M
Mechanisms regulating the B lymphopoiesis fetal/adult switchR01AI113320 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI HAYAKAWA, KYOKO · 2015 to 2019
$2.0M
Origin of CD5+ B cell Lymphoma/Leukemia in MiceR01CA129330 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI HAYAKAWA, KYOKO · 2009 to 2013
$1.8M
Pre-BCR Function Selecting Novel B Cell Receptors in Chronic Lymphocytic LeukemiaRC1CA145445 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI HARDY, RICHARD R, HAYAKAWA, KYOKO · 2009 to 2010
$971k
NCI NIH HHS R01 CA129330NCI NIH HHS RC1 CA145445NIAID NIH HHS R01 AI026782NIAID NIH HHS R01 AI049335NIAID NIH HHS R01 AI113320
6 · The paper itself

Abstract

CD5(+) B-cell origins and their predisposition to lymphoma are long-standing issues. Transfer of fetal and adult liver BM Pro-B cells generates B cells with distinct phenotypes: fetal cells generate IgM(high) IgD(low) CD5(+) , whereas adult cells IgM(low) IgD(high) CD5(-) . This suggests a developmental switch in B lymphopoiesis, similar to the switch in erythropoiesis. Comparison of mRNA and miRNA expression in fetal and adult Pro-B cells revealed differential expression of Lin28b mRNA and Let-7 miRNA, providing evidence that this regulatory axis functions in the switch. Recent work has shown that Arid3a is a key transcription factor mediating fetal-type B-cell development. Lin28b-promoted fetal development generates CD5(+) B cells as a consequence of positively selected self-reactivity. CD5(+) B cells play important roles in clearance of apoptotic cells and in protective immune responses, but also pose a risk of progression to leukemia/lymphoma. Differential Lin28b expression in fetal and adult human B-cell precursors showed that human B-cell development may resemble mouse, with self-reactive "innate-like" B cells generated early in life. It remains to be determined whether such human B cells have a higher propensity to leukemic progression. This review describes our recent research with CD5(+) B cells and presents our perspective on their role in disease.

Indexed as

AnimalsB-LymphocytesB-Lymphocyte SubsetsCD5 AntigensFetusHumansLeukemia, B-CellLymphopoiesisPrecursor Cells, B-LymphoidCD5 AntigensB1a cellsB-cell developmentB-cell leukemiaCD5+ B cellsStem cellsTransgenic mouse models

Identifiers

PMID26339791
PMCPMC4674377
OpenAlexW1900474817

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.