Evidence map›Paper›PMID 22904299›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

CD5-dependent CK2 activation pathway regulates threshold for T cell anergy.

Christine M Sestero, Donald J McGuire, Patrizia De Sarno, Emily C Brantley, Gloria Soldevila, Robert C Axtell, Chander Raman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
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  8. Article
  9. Review
  10. Review
  11. CD5 dynamically calibrates basal NF-κB signaling in T cells during thymic development and peripheral activation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. CD5 signalosome coordinates antagonist TCR signals to control the generation of Treg cells induced by foreign antigens.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. CD5, an Undercover Regulator of TCR Signaling.Frontiers in immunology · 2018
    Review
  20. 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 4 institutions in 2 countries.

Christine M SesteroDivision of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Donald J McGuire
Patrizia De Sarno
Emily C Brantley
Gloria Soldevila
Robert C Axtell
Chander Raman
University of Alabama at Birmingham · USStanford University · USThe University of Texas MD Anderson Cancer Center · USUniversidad Nacional Autónoma de México · MX

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
Mentored Experiences in Research, Instruction and Teaching (MERIT) Program - administrative supplementK12GM088010 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHNEIDER, DAVID ALAN · 2009 to 2024
$9.2M
TRAINING PROGRAM IN RHEUMATIC DISEASES RESEARCHT32AR007450 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRIDGES, S LOUIS · 1986 to 2011
$2.2M
The Role of CD5 in B-Cell Development and AutoimmunityR01AI076562 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RAMAN, CHANDER · 2008 to 2012
$1.8M
GSK3: immunoregulator in experimental autoimmune encephalomyelitis (EAE)R01NS064261 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE SARNO, PATRIZIA · 2009 to 2012
$1.1M
Developing and Improving Institutional Animal ResourcesG20RR022807 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CARTNER, SAMUEL CORBIN · 2006 to 2006
$647k
Developing and Improving Institutional Animal ResourcesG20RR025858 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CARTNER, SAMUEL CORBIN · 2009 to 2009
$499k
NCI NIH HHS P30 CA013148NCI NIH HHS P30 CA-13148NCRR NIH HHS G20 RR022807NCRR NIH HHS G20 RR022807-01NCRR NIH HHS G20 RR025858NIAID NIH HHS AI1076562NIAID NIH HHS P30 AI027767NIAID NIH HHS R01 AI076562NIAID NIH HHS T32 AI007051NIAMS NIH HHS P30 AR048311NIAMS NIH HHS P30 AR 48311NIAMS NIH HHS P30 AR48311NIAMS NIH HHS T32 AR007450NIAMS NIH HHS T32 AR07450NIGMS NIH HHS 5K12GM088010NIGMS NIH HHS K12 GM088010NINDS NIH HHS NS064261NINDS NIH HHS R01 NS064261
6 · The paper itself

Abstract

CD5 activates casein kinase 2 (CK2), a serine/threonine kinase that constitutively associates with the CK2-binding domain at the end of its cytoplasmic tail. To determine the physiological significance of CD5-dependent CK2 activation in T cells, we generated a knock-in mouse that expresses a CD5 protein containing a microdeletion with selective inability to interact with CK2 (CD5ΔCK2BD). The levels of CD5 on developing and mature T cell populations from CD5ΔCK2BD mice and CD5 wild-type (WT) mice were similar. The thymus of CD5ΔCK2BD mice contained fewer double-positive thymocytes than did that of both CD5WT and CD5 knockout (KO) mice, although the numbers of all other immature and mature T cell populations were unaltered. CD5ΔCK2BD T cells hypoproliferated and exhibited enhanced activation-induced cell death when stimulated with anti-CD3 or cognate peptide in comparison with CD5WT T cells. We also found that functional CD5-dependent CK2 signaling was necessary for efficient differentiation of naive CD4+ T cells into Th2 and Th17 cells, but not Th1 cells. We previously showed that experimental autoimmune encephalomyelitis (EAE) in CD5KO mice was less severe and delayed in onset than in CD5WT mice. Remarkably, CD5ΔCK2BD mice recapitulated both EAE severity and disease onset of CD5KO mice. Increasing the immunization dose of myelin oligodendrocyte glycoprotein 35-55 peptide, a model that mimics high-dose tolerance, led to decreased severity of EAE in CD5WT mice but not in CD5KO or CD5ΔCK2BD mice. This property was recapitulated in in vitro restimulation assays. These results demonstrate that CD5-CK2 signaling sets the threshold for T cell responsiveness and is necessary for efficient generation of Th2 and Th17 cells.

Indexed as

AnimalsCasein Kinase IICD5 AntigensCell DifferentiationClonal AnergyEncephalomyelitis, Autoimmune, ExperimentalEnzyme ActivationFemaleGene Knock-In TechniquesMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicSignal TransductionTh17 CellsCasein Kinase IICD5 AntigensCd5 protein, mouse

Identifiers

PMID22904299
PMCPMC3436980
OpenAlexW2120194551

What OpenQuestion holds

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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.