Evidence map›Paper›PMID 17967905›Full record

ArticleThe Journal of experimental medicine2007

Reduced receptor editing in lupus-prone MRL/lpr mice.

Jennifer L Lamoureux, Lisa C Watson, Marie Cherrier, Patrick Skog, David Nemazee, Ann J Feeney

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. B-Cell Receptor Repertoire: Recent Advances in Autoimmune Diseases.Clinical reviews in allergy & immunology · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. Trifluoperazine Inhibits Mesangial Cell Proliferation by Arresting Cell Cycle-Dependent Mechanisms.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  6. Mechanisms of central tolerance for B cells.Nature reviews. Immunology · 2017
    Review
  7. YY1 plays an essential role at all stages of B-cell differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  8. Article
  9. Article
  10. Article
  11. B cell tolerance and positive selection in lupus.Journal of immunology (Baltimore, Md. : 1950) · 2012
    Article
  12. Article
  13. Selection of individual VH genes occurs at the pro-B to pre-B cell transition.Journal of immunology (Baltimore, Md. : 1950) · 2011
    Article
  14. B cell receptor editing in tolerance and autoimmunity.Annals of the New York Academy of Sciences · 2011
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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 at 1 institution in 1 country.

Jennifer L LamoureuxDepartment of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Lisa C Watson
Marie Cherrier
Patrick Skog
David Nemazee
Ann J Feeney
Scripps Research Institute · US

Funding

BLOOD SYSTEMS IN COAGULATION AND VESSEL DISEASET32HL007195 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 1985 to 2011
$5.1M
RECEPTOR EDITING IN B-CELLSR01AI033608 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 1993 to 2010
$3.7M
Receptor Editing in Autoimmune and Normal MiceR01AI061167 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI FEENEY, ANN J · 2005 to 2009
$2.0M
NHLBI NIH HHS T32 HL007195NHLBI NIH HHS T32 HL07195NIAID NIH HHS R01 AI033608NIAID NIH HHS R01 AI061167NIAID NIH HHS R01 AI61167
6 · The paper itself

Abstract

The initial B cell repertoire contains a considerable proportion of autoreactive specificities. The first major B cell tolerance checkpoint is at the stage of the immature B cell, where receptor editing is the primary mode of eliminating self-reactivity. The cells that emigrate from the bone marrow have a second tolerance checkpoint in the transitional compartment in the spleen. Although it is known that the second checkpoint is defective in lupus, it is not clear whether there is any breakdown in central B cell tolerance in the bone marrow. We demonstrate that receptor editing is less efficient in the lupus-prone strain MRL/lpr. In an in vitro system, when receptor-editing signals are given to bone marrow immature B cells by antiidiotype antibody or after in vivo exposure to membrane-bound self-antigen, MRL/lpr 3-83 transgenic immature B cells undergo less endogenous rearrangement and up-regulate recombination activating gene messenger RNA to a lesser extent than B10 transgenic cells. CD19, along with immunoglobulin M, is down-regulated in the bone marrow upon receptor editing, but the extent of down-regulation is fivefold less in MRL/lpr mice. Less efficient receptor editing could allow some autoreactive cells to escape from the bone marrow in lupus-prone mice, thus predisposing to autoimmunity.

Indexed as

AnimalsB-LymphocytesBone Marrow CellsCells, CulturedGenetic Predisposition to DiseaseInterleukin-7Lupus Erythematosus, SystemicMiceMice, Inbred MRL lprMice, Inbred StrainsMice, TransgenicPolymerase Chain ReactionReceptors, Antigen, B-CellRNA EditingInterleukin-7Receptors, Antigen, B-Cell

Identifiers

PMID17967905
PMCPMC2118512
OpenAlexW2103143949

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.