Evidence map›Paper›PMID 22511718›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Toll-like receptor 4-activated B cells out-compete Toll-like receptor 9-activated B cells to establish peripheral immunological tolerance.

Melanie P Matheu, Yan Su, Milton L Greenberg, Caroline A Blanc, Ian Parker, David W Scott, Michael D Cahalan

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Regulatory T cells suppress Th17 cell CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  2. Review
  3. Oncoimmunology · 2015
    Article
  4. Two-photon imaging of cellular dynamics in the mouse spinal cord.Journal of visualized experiments : JoVE · 2015
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Orai1 function is essential for T cell homing to lymph nodes.Journal of immunology (Baltimore, Md. : 1950) · 2013
    Article
  11. 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

7 authors at 3 institutions in 2 countries.

Melanie P MatheuDepartment of Physiology and Biophysics, University of California, Irvine, CA 92697, USA.
Yan Su
Milton L Greenberg
Caroline A Blanc
Ian Parker
David W Scott
Michael D Cahalan
Uniformed Services University of the Health Sciences · USUniversity of California, Irvine · USUniversity of Maryland, Baltimore · US

Funding

Elementary Events of Intracellular Calcium SignalingR37GM048071 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARKER, IAN · 2011 to 2020
$5.3M
THE ROLE OF ION CHANNELS IN LYMPHOCYTE ACTIVATIONR01GM041514 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAHALAN, MICHAEL D · 1988 to 2013
$5.2M
SPATIAL AND TEMPORAL ASPECTS OF INSP3 SIGNALLINGR01GM048071 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARKER, IAN · 1992 to 2010
$3.9M
GENE THERAPEUTIC APPROACH FOR TOLERANCE INDUCTIONR01AI035622 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SCOTT, DAVID WILLIAM · 1997 to 2013
$3.7M
NIAID NIH HHS AI035622NIAID NIH HHS R01 AI035622NIGMS NIH HHS GM-41514NIGMS NIH HHS GM-48071NIGMS NIH HHS R01 GM041514NIGMS NIH HHS R01 GM048071NIGMS NIH HHS R37 GM048071
6 · The paper itself

Abstract

B-cell-induced peripheral T-cell tolerance is characterized by suppression of T-cell proliferation and T-cell-dependent antibody production. However, the cellular interactions that underlie tolerance induction have not been identified. Using two-photon microscopy of lymph nodes we show that tolerogenic LPS-activated membrane-bound ovalbumin (mOVA) B cells (LPS B cells) establish long-lived, highly motile conjugate pairs with responding antigen-specific OTII T cells but not with antigen-irrelevant T cells. Treatment with anti-CTLA-4 disrupts persistent B-cell-T-cell (B-T) contacts and suppresses antigen-specific tolerance. Nontolerogenic CpG-activated mOVA B cells (CpG B cells) also form prolonged, motile conjugates with responding OTII T cells when transferred separately. However, when both tolerogenic and nontolerogenic B-cell populations are present, LPS B cells suppress long-lived CpG B-OTII T-cell interactions and exhibit tolerogenic dominance. Contact of LPS B cells with previously established B-T pairs resulted in partner-swapping events in which LPS B cells preferentially migrate toward and disrupt nontolerogenic CpG mOVA B-cell-OTII T-cell pairs. Our results demonstrate that establishment of peripheral T-cell tolerance involves physical engagement of B cells with the responding T-cell population, acting in a directed and competitive manner to alter the functional outcome of B-T interactions.

Indexed as

Adoptive TransferAnimalsAntibodies, MonoclonalB-LymphocytesCTLA-4 AntigenFlow CytometryLymph NodesMiceOvalbuminPeripheral ToleranceStatistics, NonparametricT-LymphocytesToll-Like Receptor 4Toll-Like Receptor 9Antibodies, MonoclonalCTLA-4 AntigenOvalbuminToll-Like Receptor 4Toll-Like Receptor 9

Identifiers

PMID22511718
PMCPMC3356607
OpenAlexW2134139235

What OpenQuestion holds

Textmetadata
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.