Evidence map›Paper›PMID 20807702›Full record

ArticleJournal of leukocyte biology2010

TRAIL-expressing CD8+ T cells mediate tolerance following soluble peptide-induced peripheral T cell deletion.

Prajwal Gurung, Tamara A Kucaba, Stephen P Schoenberger, Thomas A Ferguson, Thomas S Griffith

Open access · greenAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2010. 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
0.9field-weighted citation impact, top 25% 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, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Impact of sepsis on CD4 T cell immunity.Journal of leukocyte biology · 2014
    Review
  6. Review
  7. Review
  8. Article
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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

5 authors at 2 institutions in 1 country.

Prajwal GurungDepartment of Urology, University of Iowa, Iowa City, Iowa 52242-1089, USA.
Tamara A Kucaba
Stephen P Schoenberger
Thomas A Ferguson
Thomas S Griffith
University of Iowa · USLa Jolla Institute for Immunology · US

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Steven Bassnett · 1985 to 2026
$18.4M
MODULATION OF ACAID BY MONOCLONAL ANTIBODIES TO TSFR01EY006765 · NEI · WASHINGTON UNIVERSITY · PI FERGUSON, THOMAS ALMON · 1987 to 2011
$5.4M
REGULATION OF IMMUNITY BY DEAD CELLSR01EY015570 · NEI · WASHINGTON UNIVERSITY · PI FERGUSON, THOMAS ALMON · 2005 to 2012
$3.0M
TRAIL-mediated regulation of T help for CTLR01CA081261 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SCHOENBERGER, STEPHEN PHILIP · 2000 to 2009
$2.7M
TRAIL-expressing Recombinant Adenovirus Based Immunotherapy for RCCR01CA109446 · NCI · UNIVERSITY OF MINNESOTA · PI GRIFFITH, THOMAS S · 2004 to 2013
$2.6M
Apoptotic cells induce tolerance through TRAIL-expressing CD8+ regulatory T cellsR56AI077565 · NIAID · UNIVERSITY OF IOWA · PI GRIFFITH, THOMAS S · 2009 to 2009
$372k
PATHOGENESIS OF UVEITIS IN HLA B27 TRANSGENIC RATSF32EY006765 · NEI · OREGON HEALTH AND SCIENCE UNIVERSITY · PI MARTIN, TAMMY M · 1996 to 1998
–
NCI NIH HHS CA109446NCI NIH HHS CA81261NCI NIH HHS R01 CA081261NCI NIH HHS R01 CA109446NEI NIH HHS EY015570NEI NIH HHS EY02687NEI NIH HHS EY06765NEI NIH HHS F32 EY006765NEI NIH HHS P30 EY002687NEI NIH HHS R01 EY006765NEI NIH HHS R01 EY015570NIAID NIH HHS AI 077565NIAID NIH HHS R56 AI077565
6 · The paper itself

Abstract

Peripheral tolerance controls the action of self-reactive T cells that escape thymic deletion. We showed previously that deletion of Ag-specific CD4+ T cells induced a CD8+ T(reg) population that maintained tolerance by deleting T cells with the same Ag specificity. The present study explored the mechanism of action of these CD8+ T(reg). Following OT-II T cell deletion by soluble OVA₃₂₃₋₃₃₉, B6 mice were unresponsive to challenge after CFA/OVA immunization, and Trail⁻/⁻ or Dr5⁻/⁻ mice were immune, although all strains displayed similar OT-II peripheral deletion. Interestingly, B6 mice remained tolerant to OVA even after a second infusion of OT-II T cells. Tolerance could be transferred to naïve recipients using CD8+ T cells from B6 or Dr5⁻/⁻ mice that experienced peptide-induced peripheral OT-II deletion but not from Trail⁻/⁻ mice. Subsequent investigation found that the mechanism of action of the CD8+ T(reg) was TRAIL-mediated OT-II T cell deletion in a TCR-specific manner. Furthermore, the tolerance was transient, as it was established by 14 days after peptide injection but lost by Day 56. Together, these data provide evidence to suggest that the mechanism behind transient peripheral tolerance induced following T cell deletion is the cytotoxic activity of TRAIL-expressing CD8+ T(reg).

Indexed as

Immune ToleranceLymphocyte DepletionAnimalsCD8-Positive T-LymphocytesCytotoxicity, ImmunologicMiceOvalbuminReceptors, Antigen, T-CellReceptors, TNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing LigandOvalbuminReceptors, Antigen, T-CellReceptors, TNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing LigandTnfsf10 protein, mouse

Identifiers

PMID20807702
PMCPMC2996898
OpenAlexW2159304397

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.