Evidence map›Paper›PMID 32429209›Full record

ArticleCells2020

Liver Sinusoidal Endothelial Cells Contribute to Hepatic Antigen-Presenting Cell Function and Th17 Expansion in Cirrhosis.

Esther Caparrós, Oriol Juanola, Isabel Gómez-Hurtado, Amaya Puig-Kroger, Paula Piñero, Pedro Zapater, Raquel Linares, Fabián Tarín, Sebastián Martínez-López, Jordi Gracia-Sancho and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  12. Role of liver sinusoidal endothelial cells in liver diseases.Nature reviews. Gastroenterology & hepatology · 2021
    Review
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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

12 authors at 4 institutions in 1 country.

Esther CaparrósDpto Medicina Clínica, Universidad Miguel Hernández, 03550 San Juan de Alicante, Spain.
Oriol JuanolaDpto Medicina Clínica, Universidad Miguel Hernández, 03550 San Juan de Alicante, Spain.
Isabel Gómez-HurtadoCIBERehd, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Amaya Puig-KrogerInstituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.
Paula PiñeroInstituto ISABIAL, Hospital General Universitario Alicante, 03010 Alicante, Spain.
Pedro ZapaterCIBERehd, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Raquel LinaresDpto Medicina Clínica, Universidad Miguel Hernández, 03550 San Juan de Alicante, Spain.
Fabián TarínInstituto ISABIAL, Hospital General Universitario Alicante, 03010 Alicante, Spain.
Sebastián Martínez-LópezDpto Medicina Clínica, Universidad Miguel Hernández, 03550 San Juan de Alicante, Spain.ORCID 0000-0003-1720-845X
Jordi Gracia-SanchoCIBERehd, Instituto de Salud Carlos III, 28029 Madrid, Spain.ORCID 0000-0001-7736-4089
José M González-NavajasCIBERehd, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Rubén FrancésDpto Medicina Clínica, Universidad Miguel Hernández, 03550 San Juan de Alicante, Spain.ORCID 0000-0001-5105-1201
Universitat de Miguel Hernández d'Elx · ESHospital General Universitario de Alicante Doctor Balmis · ESInstituto de Salud Carlos III · ESHospital General Universitario Gregorio Marañón · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic immune function is compromised during cirrhosis. This study investigated the immune features of liver sinusoidal endothelial cells (LSECs) in two experimental models of cirrhosis. Dendritic cells, hepatic macrophages, and LSECs were isolated from carbon tetrachloride and bile duct-ligated rats. Gene expression of innate receptors, bacterial internalization, co-stimulatory molecules induction, and CD4+ T cell activation and differentiation were evaluated. Induced bacterial peritonitis and norfloxacin protocols on cirrhotic rats were also carried out. LSECs demonstrated an active immunosurveillance profile, as shown by transcriptional modulation of different scavenger and cell-adhesion genes, and their contribution to bacterial internalization. LSECs significantly increased their expression of CD40 and CD80 and stimulated CD4+ T cell activation marker CD71 in both models. The pro-inflammatory Th17 subset was expanded in CCl

Indexed as

Adaptive ImmunityAnimalsAntigen-Presenting CellsBiomarkersCell DifferentiationCell MembraneCell ProliferationEndocytosisEndothelial CellsEscherichia coliImmunity, InnateLiverLiver CirrhosisLymphocyte ActivationMaleMicrobial ViabilityBiomarkersNorfloxacinReceptors, Immunologicdendritic cellshepatic macrophagesKeywords: cirrhosisliver sinusoidal endothelial cellsnorfloxacinTh cells

Identifiers

PMID32429209
PMCPMC7290576
OpenAlexW3025612840

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.