Evidence map›Paper›PMID 19737142›Full record

ArticleClinical and experimental immunology2009

Chronic antigenic stimuli as a possible explanation for the immunodepression caused by liver cirrhosis.

M Márquez, C Fernández-Gutiérrez, M Montes-de-Oca, M J Blanco, F Brun, C Rodríguez-Ramos, J A Girón-González

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Liver cirrhosis and immune dysfunction.International immunology · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Case reports in hepatology · 2020
    Article
  10. Observational
  11. Article
  12. Article
  13. Immune Dysfunction in Cirrhosis.Journal of clinical and translational hepatology · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Immune dysfunction in cirrhosis.World journal of gastroenterology · 2014
    Review
  20. Review
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

7 authors at 1 institution in 1 country.

M MárquezInfectious Diseases Units, Internal Medicine, Hospital Universitario Puerta del Mar, Cadiz, Spain.
C Fernández-Gutiérrez
M Montes-de-Oca
M J Blanco
F Brun
C Rodríguez-Ramos
J A Girón-González
Hospital Universitario Puerta del Mar · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objectives of this work were the analysis of the functional characteristics of circulating monocytes and T lymphocytes in patients with liver cirrhosis, and evaluation of the relationship with an increased exposure to antigens due to bacterial translocation. Forty patients with liver cirrhosis (20 with compensated cirrhosis and 20 with ascitic decompensation) and 20 healthy control subjects were studied. Bacterial translocation was evaluated by serum levels of lipopolysaccharide binding protein (LBP). Macrophage activation was studied by CD40 antigen expression. T lymphocytes were analysed for activation (CD25(+), CD122(+)), effector function (CD8(+)CD45RO(+)CD57(+)), apoptosis (CD95(+)) and regulatory abilities, either by analysis of the membrane expression of co-stimulatory molecules CD80, CD86 and CD28, or by quantification of regulatory T cells CD4(+)CD25(high)forkhead box P3 (FoxP3). The percentage of activated monocytes and T lymphocytes in patients was increased significantly. The proportions of effector senescent cells and of those near to apoptosis were also significantly higher. With respect to these proportions, there were no significant differences between patients in function of the presence or absence of decompensation or in function of the increased or normal values of LBP. Conversely, those patients with elevated levels of LBP presented a significantly higher frequency of regulatory T cells than those with normal levels. In conclusion, patients with liver cirrhosis showed an intensive activation state with a higher percentage of cells committed to activation-induced death, even in non-advanced stages. It is possible that bacterial permeability and endotoxaemia contribute to the expansion of those lymphocyte populations implicated in the prevention of a more severe antigen-induced immunopathology.

Indexed as

Immune ToleranceAcute-Phase ProteinsAgedAntigens, BacterialBacterial TranslocationCarrier ProteinsFemaleHumansInflammation MediatorsLipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsLiver CirrhosisLymphocyte ActivationLymphopeniaMacrophage ActivationMaleAcute-Phase ProteinsAntigens, BacterialCarrier ProteinsInflammation MediatorsLipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsMembrane Glycoproteins

Identifiers

PMID19737142
PMCPMC2768811
OpenAlexW2094228659

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.