Evidence map›Paper›PMID 29686680›Full record

ArticleFrontiers in immunology2018

Activation of the MEK-ERK Pathway Is Necessary but Not Sufficient for Breaking Central B Cell Tolerance.

Sarah A Greaves, Jacob N Peterson, Raul M Torres, Roberta Pelanda

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 36% 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, 20 citations in OpenAlex.

  1. Review
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  11. Central human B cell tolerance manifests with a distinctive cell phenotype and is enforced via CXCR4 signaling in hu-mice.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Sarah A GreavesDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
Jacob N PetersonDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
Raul M TorresDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
Roberta PelandaDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
University of Colorado Denver · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Chemokine response in B cell development and functionR01AI052157 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2002 to 2017
$5.4M
Tolerance in Polyclonal and Oligoclonal Immune SystemsR01AI052310 · NIAID · UNIVERSITY OF COLORADO DENVER · PI PELANDA, ROBERTA · 2003 to 2017
$5.0M
Humoral Immunity by Anergic B cellsR01AI136534 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2018 to 2022
$2.6M
Testing an alternative model of central B cell toleranceR21AI131639 · NIAID · UNIVERSITY OF COLORADO DENVER · PI PELANDA, ROBERTA · 2017 to 2018
$428k
Tolerance in Polyclonal and Oligoclonal Immune SystemsR56AI052310 · NIAID · NATIONAL JEWISH HEALTH · PI PELANDA, ROBERTA · 2007 to 2007
$363k
NCI NIH HHS P30 CA046934NIAID NIH HHS R01 AI052157NIAID NIH HHS R01 AI052310NIAID NIH HHS R01 AI136534NIAID NIH HHS R21 AI131639NIAID NIH HHS R56 AI052310
6 · The paper itself

Abstract

Newly generated bone marrow B cells are positively selected into the peripheral lymphoid tissue only when they express a B cell receptor (BCR) that is nonautoreactive or one that binds self-antigen with only minimal avidity. This positive selection process, moreover, is critically contingent on the ligand-independent tonic signals transduced by the BCR. We have previously shown that when autoreactive B cells express an active form of the rat sarcoma (RAS) oncogene, they upregulate the receptor for the B cell activating factor (BAFFR) and undergo differentiation

Indexed as

MAP Kinase Signaling SystemAnimalsAntibody FormationB-Cell Activation Factor ReceptorB-LymphocytesCell DifferentiationCentral ToleranceEnzyme ActivationExtracellular Signal-Regulated MAP KinasesFemaleGene Expression RegulationGenetic VectorsMaleMiceMice, KnockoutMice, TransgenicB-Cell Activation Factor ReceptorExtracellular Signal-Regulated MAP KinasesReceptors, Antigen, B-CellTnfrsf13c protein, mouseautoreactive B cellsB cell developmentB cellsB cell toleranceBCR signalingERKMAP kinasemouse models

Identifiers

PMID29686680
PMCPMC5900439
OpenAlexW2792817390

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.