Evidence map›Paper›PMID 22365785›Full record

ArticleJournal of autoimmunity2012

Potentially autoreactive naturally occurring transitional T3 B lymphocytes exhibit a unique signaling profile.

Ganna A Liubchenko, Holly C Appleberry, V Michael Holers, Nirmal K Banda, Van C Willis, Taras Lyubchenko

Abstract read
In one paragraph

Article in Journal of autoimmunity, 2012. 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
0.9field-weighted citation impact, top 28% 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, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Overview of the Different Classes of Small RNAs During B-Cell Development.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  6. Anti-HIV-1 B cell responses are dependent on B cell precursor frequency and antigen-binding affinity.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Autoimmunity in 2012.Clinical reviews in allergy & immunology · 2013
    Review
  12. 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.

Ganna A LiubchenkoDivision of Rheumatology, University of Colorado Denver School of Medicine, Mail Stop B115, 1775 Aurora Ct., Aurora, CO 80045, USA.
Holly C Appleberry
V Michael Holers
Nirmal K Banda
Van C Willis
Taras Lyubchenko
University of Colorado Denver · US

Funding

Mechanisms of B cell activation by Complement Receptor 2K01AR056023 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI LYUBCHENKO, TARAS · 2009 to 2013
$635k
NIAMS NIH HHS K01 AR056023
6 · The paper itself

Abstract

B lymphocytes exhibit phenotypic differences that correlate with their developmental or functional stages and affect humoral immune responses. One recently described subset of naturally occurring immature transitional type 3 (T3) B lymphocytes is believed to consist of potentially autoimmune cells whose signaling properties have not been studied in detail. This study characterizes intracellular signaling in T3 B cells in wildtype C57BL/6 mice. Protein phosphorylation and Ca(2+) responses upon B-cell antigen receptor (BCR) engagement were measured by multicolor flow cytometry. We observed high baseline signaling activity and reduced BCR-mediated responses in T3 cells, which confirmed their anergy - a functional state in which lymphocytes recognize chronically present self-antigens but cannot produce immune response due to intrinsic signaling inhibition. Our results also revealed a previously unknown T3-specific phosphorylation pattern of 24 key signaling molecules involved in BCR signal transduction. These characteristics reflect the balance between stimulatory and inhibitory BCR signaling pathways in anergy. Results obtained in the collagen-induced arthritis model demonstrate the loss of anergy in T3 B cells during the onset of the disease. Our findings provide rationale for further investigating alterations in B-cell signaling patterns as earliest functional biomarkers of changes in the immune tolerance of autoreactive B cells.

Indexed as

AutoimmunitySignal TransductionAnimalsArthritis, ExperimentalB-LymphocytesCalciumClonal AnergyMiceMice, Inbred C57BLMice, Inbred DBAPhenotypePhosphorylationReceptors, Antigen, B-CellReproducibility of ResultsCalciumReceptors, Antigen, B-Cell

Identifiers

PMID22365785
PMCPMC3358596
OpenAlexW2024091442

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.