Evidence map›Paper›PMID 18941180›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Fas expression on antigen-specific T cells has costimulatory, helper, and down-regulatory functions in vivo for cytotoxic T cell responses but not for T cell-dependent B cell responses.

Irina Puliaeva, Roman Puliaev, Andrei Shustov, Mark Haas, Charles S Via

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. CD4Frontiers in cell and developmental biology · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Life in the Fas lane: differential outcomes of Fas signaling.Cellular and molecular life sciences : CMLS · 2013
    Review
  11. Article
  12. Review
  13. Article
  14. Pro- and anti-apoptotic CD95 signaling in T cells.Cell communication and signaling : CCS · 2011
    Article
  15. Article
  16. Article
  17. Review
  18. 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

5 authors at 4 institutions in 1 country.

Irina PuliaevaDepartment of Pathology, Uniformed Services University of Health Sciences, Bethesda, MD 20814, USA.
Roman Puliaev
Andrei Shustov
Mark Haas
Charles S Via
Uniformed Services University of the Health Sciences · USJohns Hopkins University · USUniversity of Health SciencesUniversity of Maryland, Baltimore · US

Funding

IMMUNOPATHOGENESIS OF LUPUSR01AI047466 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VIA, CHARLES S. · 2001 to 2012
$3.2M
Immunopathogenesis of LupusR56AI047466 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI VIA, CHARLES S. · 2014 to 2014
$189k
NIAID NIH HHS AI 47466NIAID NIH HHS R01 AI047466NIAID NIH HHS R56 AI047466
6 · The paper itself

Abstract

Fas-mediated apoptosis is an important contributor to contraction of Ag-driven T cell responses acting only on activated Ag-specific T cells. The effects of targeted Fas deletion on selected cell populations are well described however little is known regarding the consequences of Fas deletion on only activated Ag-specific T cells. We addressed this question using the parent-into-F(1) (P-->F(1)) model of acute or chronic (lupus-like) graft-vs-host disease (GVHD) as a model of either a CTL-mediated or T-dependent B cell-mediated response, respectively. By transferring Fas-deficient lpr donor T cells into Fas-intact F(1) hosts, the in vivo role of Ag-specific T cell Fas can be determined. Our results demonstrate a novel dichotomy of Ag-specific T cell Fas function in that: 1) Fas expression on Ag-activated T cells has costimulatory, helper, and down-regulatory roles in vivo and 2) these roles were observed only in a CTL response (acute GVHD) and not in a T-dependent B cell response (chronic GVHD). Specifically, CD4 T cell Fas expression is important for optimal CD4 initial expansion and absolutely required for help for CD8 effector CTL. Donor CD8 T cell Fas expression played an important but not exclusive role in apoptosis and down-regulation. By contrast, CD4 Fas expression played no detectable role in modulating chronic GVHD induction or disease expression. These results demonstrate a novel role for Ag-specific T cell Fas expression in in vivo CTL responses and support a review of the paradigm by which Fas deficiency accelerates lupus in MRL/lpr lupus-prone mice.

Indexed as

Acute DiseaseAnimalsB-LymphocytesCD4-Positive T-LymphocytesCell Line, TumorCells, CulturedCrosses, GeneticDown-RegulationEpitopes, T-Lymphocytefas ReceptorGraft vs Host DiseaseLupus NephritisLymphocyte ActivationMaleMiceMice, Inbred C57BLEpitopes, T-Lymphocytefas Receptor

Identifiers

PMID18941180
PMCPMC2775525
OpenAlexW1559302243

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.