Evidence map›Paper›PMID 10792370›Full record

ArticleClinical and experimental immunology2000

Cytolytic mechanisms of intraepithelial lymphocytes in coeliac disease (CoD).

R Ciccocioppo, A Di Sabatino, R Parroni, S D'alò, M A Pistoia, C Doglioni, M G Cifone, G R Corazza

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Evolving Therapy for Celiac Disease.Frontiers in pediatrics · 2019
    Review
  6. Review
  7. Review
  8. Celiac disease: understanding the gluten-free diet.European journal of nutrition · 2017
    Review
  9. Mesenchymal stem cells as potential therapeutic approaches in celiac disease.Gastroenterology and hepatology from bed to bench · 2016
    Review
  10. Are stem cells a potential therapeutic tool in coeliac disease?Cellular and molecular life sciences : CMLS · 2015
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

8 authors at 3 institutions in 1 country.

R CiccocioppoGastroenterology Unit, IRCCS Policlinico S. Matteo, University of Pavia, Pavia, Italy.
A Di Sabatino
R Parroni
S D'alò
M A Pistoia
C Doglioni
M G Cifone
G R Corazza
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of L'Aquila · ITUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effector arm of the mucosal immune system comprises lymphocytes scattered at intraepithelial and lamina propria levels. Intraepithelial lymphocytes (IEL) are a large population of oligoclonal resting cells which exhibit phenotypic and functional characteristics of cytolytic T cells when activated. Several mechanisms have been demonstrated to account for their cytotoxicity. Among them, one is mediated by perforin and granzyme molecules, another is mediated by Fas ligand (FasL) which delivers apoptotic signals through Fas receptor on target cells. There is good evidence that a flat intestinal mucosa may be produced by activated T cells. The aim of our study was to evaluate FasL and perforin expression by IEL, and its possible correlation with the increased enterocyte apoptosis in coeliac mucosa. Endoscopic duodenal biopsy specimens from 10 untreated coeliac patients, 10 treated coeliac patients, and 10 biopsied controls were evaluated for enterocyte apoptosis by terminal deoxynucleotidyl transferase-mediated digoxigenin-deoxyuridine triphosphate nick end label method, for perforin expression by immunohistochemistry, and for FasL expression by immunocytochemistry. In untreated CoD there was a significant increase of percentage of both FasL+ and perforin+ IEL which positively correlated with enterocyte apoptosis in comparison with controls. All these parameters were significantly lower in treated CoD, even though they did not normalize. Our study demonstrates that in untreated CoD FasL and perforin expression by IEL is increased, and significantly correlates with the level of enterocyte apoptosis.

Indexed as

AdolescentAdultAgedCD3 ComplexCeliac DiseaseCytotoxicity, ImmunologicFas Ligand ProteinFemaleHumansImmunoenzyme TechniquesIntestinal MucosaMaleMembrane GlycoproteinsMiddle AgedPerforinPore Forming Cytotoxic ProteinsCD3 ComplexFASLG protein, humanFas Ligand ProteinMembrane GlycoproteinsPerforinPore Forming Cytotoxic Proteins

Identifiers

PMID10792370
PMCPMC1905653
OpenAlexW2061478907

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.