Evidence map›Paper›PMID 29876779›Full record

ArticleDigestive diseases and sciences2018

Expression of α-Defensins, CD20+ B-lymphocytes, and Intraepithelial CD3+ T-lymphocytes in the Intestinal Mucosa of Patients with Liver Cirrhosis: Emerging Mediators of Intestinal Barrier Function.

Georgios I Tsiaoussis, Eleni C Papaioannou, Eleni P Kourea, Stelios F Assimakopoulos, Georgios I Theocharis, Michalis Petropoulos, Vasileios I Theopistos, Georgia G Diamantopoulou, Zoi Lygerou, Iris Spiliopoulou and 1 more

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Article in Digestive diseases and sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Human α-Defensin 5International journal of molecular sciences · 2023
    Article
  4. The shaping of gut immunity in cirrhosis.Frontiers in immunology · 2023
    Review
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Georgios I TsiaoussisDepartment of Gastroenterology, University Hospital of Patras, CP 26504, Patras, Greece. tsiaoussisgeorgios@yahoo.com.
Eleni C PapaioannouDepartment of Pathology, School of Medicine, University of Patras, CP 26504, Patras, Greece.
Eleni P KoureaDepartment of Pathology, School of Medicine, University of Patras, CP 26504, Patras, Greece.
Stelios F AssimakopoulosDepartment of Internal Medicine, University Hospital of Patras, CP 26504, Patras, Greece.
Georgios I TheocharisDepartment of Gastroenterology, University Hospital of Patras, CP 26504, Patras, Greece.
Michalis PetropoulosDepartment of General Biology, School of Medicine, University of Patras, CP 26504, Patras, Greece.
Vasileios I TheopistosDepartment of Gastroenterology, University Hospital of Patras, CP 26504, Patras, Greece.
Georgia G DiamantopoulouDepartment of Gastroenterology, University Hospital of Patras, CP 26504, Patras, Greece.
Zoi LygerouDepartment of General Biology, School of Medicine, University of Patras, CP 26504, Patras, Greece.
Iris SpiliopoulouDepartment of Microbiology, School of Medicine, University of Patras, CP 26504, Patras, Greece.
Konstantinos C ThomopoulosDepartment of Gastroenterology, University Hospital of Patras, CP 26504, Patras, Greece.
General University Hospital of Patras · GRUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe present study investigates the role of innate and adaptive immune system of intestinal mucosal barrier function in cirrhosis.

methodsForty patients with decompensated (n = 40, group A), 27 with compensated cirrhosis (n = 27, group B), and 27 controls (n = 27, group C) were subjected to duodenal biopsy. Expression of α-defensins 5 and 6 at the intestinal crypts was evaluated by immunohistochemistry and immunofluorescence. Serum endotoxin, intestinal T-intraepithelial, and lamina propria B-lymphocytes were quantified.

resultsCirrhotic patients presented higher endotoxin concentrations (p < 0.0001) and diminished HD5 and HD6 expression compared to healthy controls (p = 0.000287, p = 0.000314, respectively). The diminished HD5 and HD6 expressions were also apparent among the decompensated patients compared to compensated group (p = 0.025, p = 0.041, respectively). HD5 and HD6 expressions were correlated with endotoxin levels (r = -0.790, p < 0.0001, r = - 0.777, p < 0.0001, respectively). Although intraepithelial T-lymphocytes were decreased in group A compared to group C (p = 0.002), no notable alterations between groups B and C were observed. The B-lymphocytic infiltrate did not differ among the investigated groups.

conclusionsThese data demonstrate that decreased expression of antimicrobial peptides may be considered as a potential pathophysiological mechanism of intestinal barrier dysfunction in liver cirrhosis, while remodeling of gut-associated lymphoid tissue as an acquired immune response to bio-pathogens remains an open field to illuminate.

Indexed as

Immunity, Mucosalalpha-DefensinsEndotoxinsFemaleHumansLiver CirrhosisLymphocytesLymphoid TissueMaleMiddle AgedPaneth CellsProspective Studiesalpha-DefensinsEndotoxinsAntimicrobial peptidesBacterial translocationEndotoxinGut-associated lymphoid tissueMucosal defensePaneth cells

Identifiers

PMID29876779
OpenAlexW2806764969

What OpenQuestion holds

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Registered trials

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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.