Evidence map›Paper›PMID 10510080›Full record

ArticleThe Journal of experimental medicine1999

Selection at multiple checkpoints focuses V(H)12 B cell differentiation toward a single B-1 cell specificity.

C Tatu, J Ye, L W Arnold, S H Clarke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-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

12 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Innate B Cells: the Archetype of Protective Immune Cells.Clinical reviews in allergy & immunology · 2020
    Review
  4. Expression of plasma cell alloantigen 1 defines layered development of B-1a B-cell subsets with distinct innate-like functions.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  5. Article
  6. Article
  7. Microanatomy of the liver immune system.Seminars in immunopathology · 2009
    Review
  8. Article
  9. Article
  10. Maintenance and loss of self-tolerance in B cells.Springer seminars in immunopathology · 2001
    Review
  11. Article
  12. 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

4 authors at 1 institution in 1 country.

C TatuDepartment of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Ye
L W Arnold
S H Clarke
University of North Carolina at Chapel Hill · US

Funding

ANTISM B CELL REGULATIONR01AI043587 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CLARKE, STEPHEN H · 1998 to 2007
$2.0M
Pre-BCR expression level regulates cellular functionsR21AI029576 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CLARKE, STEPHEN H · 2002 to 2002
$287k
VARIABLE REGION GENE REPERTOIRE OF LY-1 B-CELLSR01AI029576 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CLARKE, STEPHEN H · 1990 to 2000
$254k
NIAID NIH HHS AI29576NIAID NIH HHS AI43587NIAID NIH HHS R01 AI043587
6 · The paper itself

Abstract

Phosphatidyl choline (PtC)-specific B cells segregate to the B-1 subset, where they comprise up to 10% of the B-1 repertoire. About half express V(H)12 and Vkappa4/5H and are restricted in V(H)CDR3. We have previously reported that anti-PtC V(H)CDR3 is enriched among V(H)12-expressing cells by selective elimination of pre-B cells. We report here a bias for Vkappa4/5H expression among V(H)12-expressing B cells, even among those that do not bind PtC and are not B-1. This is due in part to an inability of V(H)12 to associate with many light (L) chains but must also be due to a selective advantage in survival or clonal expansion in the periphery for Vkappa4/5H-expressing cells. Thus, the bias for Vkappa4/5H expression is independent of PtC binding, and, as segregation to B-1 occurs after Ig gene expression, it precedes segregation to the B-1 subset. In 6-1 mice, splenic B-1 cells reside in follicles but segregate to follicles distinct from those that contain B-2 cells. These data indicate that selection at multiple developmental checkpoints ensures the co-expression of an anti-PtC V(H)CDR3 and L chain in a high frequency of V(H)12 B cells. This focus toward specificity for PtC facilitates the development of a large anti-PtC B-1 repertoire.

Indexed as

Complementarity Determining RegionsAmino Acid SequenceAnimalsB-Lymphocyte SubsetsCell DifferentiationCell SurvivalCrosses, GeneticFlow CytometryGene Rearrangement, B-Lymphocyte, Heavy ChainImmunoglobulin Heavy ChainsImmunoglobulin kappa-ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionMiceMice, Inbred StrainsMice, KnockoutComplementarity Determining RegionsImmunoglobulin Heavy ChainsImmunoglobulin kappa-ChainsImmunoglobulin Light ChainsImmunoglobulin Variable RegionPhosphatidylcholines

Identifiers

PMID10510080
PMCPMC2195649
OpenAlexW1987388405

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.