Evidence map›Paper›PMID 10727450›Full record

ArticleThe Journal of clinical investigation2000

Antigen presenting cells expressing Fas ligand down-modulate chronic inflammatory disease in Fas ligand-deficient mice.

H G Zhang, M Fleck, E R Kern, D Liu, Y Wang, H C Hsu, P Yang, Z Wang, D T Curiel, T Zhou and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 57 citations in OpenAlex.

  1. FAS mediates apoptosis, inflammation, and treatment of pathogen infection.Frontiers in cellular and infection microbiology · 2025
    Review
  2. Article
  3. Review
  4. Article
  5. Review
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  7. Article
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  11. Tumor counterattack: fact or fiction?Cancer immunology, immunotherapy : CII · 2005
    Review
  12. Article
  13. Review
  14. Article
  15. Gene therapy for autoimmune disorders.Journal of clinical immunology · 2000
    Review
  16. 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

11 authors at 2 institutions in 2 countries.

H G ZhangDepartment of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama-Birmingham, Birmingham, Alabama 35294, USA.
M Fleck
E R Kern
D Liu
Y Wang
H C Hsu
P Yang
Z Wang
D T Curiel
T Zhou
J D Mountz
University of Alabama at Birmingham · USUniversity of Regensburg · DE

Funding

A multiverse analysis of the affect-alcohol use associationR01AA030744 · NIAAA · UNIVERSITY OF WASHINGTON · PI Kevin Michael King, Aidan Gregory Craver Wright · 2024 to 2026
$2.1M
ABLATION OF IMMUNE RESPONSE TO ADENOVIRUS VECTORSR01AI042900 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 1999 to 2003
$843k
GENE THERAPY TO CORRECT ARTHRITIS IN AUTOIMMUNE MICEN01AR062224 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 1996 to 2000
$328k
EXPRESSION OF TRANSGENIC TCR GENES IN AUTOIMMUNE 1PR/1PRR01AI030744 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 1991 to 1993
–
MRI GRADIENT SAFETY STUDIESR01CA062224 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI BOURLAND, JOE D · 1994 to 1997
–
NCI NIH HHS N01 AR062224NIAAA NIH HHS R01 AA030744NIAID NIH HHS R01 AI042900NIAID NIH HHS R01 AI30744NIAID NIH HHS R01-AI-42900NIAMS NIH HHS N01-AR-62224
6 · The paper itself

Abstract

We assessed the effect of modified antigen presenting cells (APCs) expressing high levels of Fas ligand (APC-FasL) on post-viral chronic inflammatory disease. FasL-deficient B6-gld/gld mice infected with murine cytomegalovirus (MCMV) cleared the virus from their lungs, kidneys, and livers within 2 weeks of infection. However, inflammation persisted in these organs for more than 8 weeks, with a chronically increased T-cell response to MCMV-infected APCs and production of autoantibodies. Administration of APC-AdFasL at 4 weeks suppressed this inflammation and diminished the T-cell response and autoantibody production. APC-AdFasL that had been transfected with ultraviolet-irradiated MCMV were more effective than uninfected APC-AdFasL in ameliorating the chronic inflammation. APC-AdFasL migrated preferentially to the spleen, where they triggered apoptosis of lymphocytes in the marginal zone of the spleen. These results confirm that Fas-mediated apoptosis is not required for clearance of virus, but is required for down-modulation of the virally induced chronic inflammatory response. This organwide effect of APC-AdFasL appears to be mediated by elimination of activated T lymphocytes in the spleen before their emigration to the target organs.

Indexed as

ApoptosisAdenoviridaeAnimalsAntigen-Presenting CellsAutoantibodiesCytomegalovirus InfectionsFas Ligand Proteinfas ReceptorFemaleGenetic VectorsHepatitis, Viral, AnimalInflammationKidneyLiverLungLung Diseases, InterstitialAutoantibodiesFas Ligand ProteinFasl protein, mousefas ReceptorMembrane Glycoproteins

Identifiers

PMID10727450
PMCPMC377462
OpenAlexW2083601744

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.