Evidence map›Paper›PMID 35330909›Full record

ArticleFrontiers in immunology2022

Reduced Plasma Extracellular Vesicle CD5L Content in Patients With Acute-On-Chronic Liver Failure: Interplay With Specialized Pro-Resolving Lipid Mediators.

María Belen Sánchez-Rodríguez, Érica Téllez, Mireia Casulleras, Francesc E Borràs, Vicente Arroyo, Joan Clària, Maria-Rosa Sarrias

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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  5. Mechanisms of immunity in acutely decompensated cirrhosis and acute-on-chronic liver failure.Liver international : official journal of the International Association for the Study of the Liver · 2025
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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

7 authors at 4 institutions in 1 country.

María Belen Sánchez-RodríguezBiochemistry and Molecular Genetics Service, Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Érica TéllezInnate Immunity Lab, Health Research Institute Germans Trias i Pujol (IGTP), Badalona, Spain.
Mireia CasullerasBiochemistry and Molecular Genetics Service, Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Francesc E BorràsInnovation in VEsicles and Cells for Application in Therapy (IVECAT), Health Research Institute Germans Trias i Pujol (IGTP), Badalona, Spain.
Vicente ArroyoEuropean Foundation for the Study of Chronic Liver Failure (EF Clif) and Grifols Chair, Barcelona, Spain.
Joan ClàriaBiochemistry and Molecular Genetics Service, Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Maria-Rosa SarriasInnate Immunity Lab, Health Research Institute Germans Trias i Pujol (IGTP), Badalona, Spain.
Consorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESEuropean Foundation for the Study of Chronic Liver Failure · ESInstitut d'Investigació en Ciències de la Salut Germans Trias i Pujol · ESCentre for Biomedical Network Research on Rare Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute-on chronic liver failure (ACLF) is a syndrome that develops in patients with acutely decompensated cirrhosis (AD). It is characterized by a systemic hyperinflammatory state, leading to multiple organ failure. Our objective was to analyze macrophage anti-inflammatory protein CD5L in plasma extracellular vesicles (EVs) and assess its as yet unknown relationship with lipid mediators in ACLF. With this aim, EVs were purified by size exclusion chromatography from the plasma of healthy subjects (HS) (n=6) and patients with compensated cirrhosis (CC) (n=6), AD (n=11) and ACLF (n=11), which were defined as positive for CD9, CD5L and CD63 and their size, number, morphology and lipid mediator content were characterized by NTA, EM, and LC-MS/MS, respectively. Additionally, plasma CD5L was quantified by ELISA in 10 HS, 20 CC and 149 AD patients (69 ACLF). Moreover, macrophage CD5L expression and the biosynthesis of specialized lipid mediators (SPMs) were characterized

Indexed as

Acute-On-Chronic Liver FailureApoptosis Regulatory ProteinsExtracellular VesiclesReceptors, ScavengerChromatography, LiquidFibrosisHumansLipidsLiver CirrhosisPrognosisSeverity of Illness IndexTandem Mass SpectrometryApoptosis Regulatory ProteinsCD5L protein, humanLipidsReceptors, Scavengercirrhosislipid autacoidsmacrophagesresolution of inflammationRvE1

Identifiers

PMID35330909
PMCPMC8940329
OpenAlexW4220830344

What OpenQuestion holds

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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.