Evidence map›Paper›PMID 25383768›Full record

ArticlePloS one2014

High levels of soluble CTLA-4 are present in anti-mitochondrial antibody positive, but not in antibody negative patients with primary biliary cirrhosis.

Daniele Saverino, Giampaola Pesce, Princey Antola, Brunetta Porcelli, Ignazio Brusca, Danilo Villalta, Marilina Tampoia, Renato Tozzoli, Elio Tonutti, Maria Grazia Alessio and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Gene and protein expression of a soluble form of CTLA-4 in a healthy dog.The Journal of veterinary medical science · 2017
    Article
  2. Article
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 7 institutions in 1 country.

Daniele SaverinoDepartment of Experimental Medicine - Section of Human Anatomy, University of Genova, Genova, Italy.
Giampaola PesceAutoimmunity Unit, Department of Internal Medicine, University of Genova, Genova, Italy.
Princey AntolaAutoimmunity Unit, Department of Internal Medicine, University of Genova, Genova, Italy.
Brunetta PorcelliDepartment of Internal Medicine, University of Siena, Siena, Italy.
Ignazio BruscaDepartment of Clinical Pathology, Buccheri La Ferla Hospital, Palermo, Italy.
Danilo VillaltaAllergology and Clinical Immunology, S. Maria degli Angeli Hospital, Pordenone, Italy.
Marilina TampoiaLaboratory of Clinical Pathology, University Hospital, Bari, Italy.
Renato TozzoliClinical Pathology, Department of Laboratory Medicine, S. Maria degli Angeli Hospital, Pordenone, Italy.
Elio TonuttiImmunopathology and Allergology Unit, S. Maria della Misericordia Hospital, Udine, Italy.
Maria Grazia AlessioDepartment of Laboratory Medicine, Biochemistry Laboratory, Riuniti Hospital, Bergamo, Italy.
Marcello BagnascoAutoimmunity Unit, Department of Internal Medicine, University of Genova, Genova, Italy.
Nicola BizzaroLaboratory of Clinical Pathology, San Antonio Hospital, Tolmezzo, Udine, Italy.
University of Genoa · ITAzienda Ospedaliera Santa Maria Degli Angeli · ITOspedale Buccheri la Ferla Fatebenefratelli · ITOspedale Santa Maria della Misericordia di Udine · ITOspedale Sant Antonio · ITUniversity of Bari Aldo Moro · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary biliary cirrhosis (PBC) is a chronic autoimmune cholestatic liver disease frequently characterized by anti-mitochondrial autoantibodies (AMA). A minority of patients are AMA-negative. Cytotoxic-T-Lymphocyte-Antigen-4 (CTLA-4) is a surface molecule expressed on activated T-cells delivering a critical negative immunoregulatory signal. A soluble form of CTLA-4 (sCTLA-4) has been detected at high concentrations in several autoimmune diseases, and its possible functional meaning has been suggested. We aimed to evaluate sCTLA-4 concentration in sera of patients with PBC and to correlate it to immunological abnormalities associated with the disease. Blood samples were collected from 82 PBC-patients diagnosed according to international criteria (44 AMA-positive/MIT3-positive and 38 AMA-negative-MIT3-negative), and 65 controls. sCTLA-4 levels were evaluated by ELISA and Western blot. Increased sCTLA-4 concentrations were found in all AMA-positive PBC-patients, but in none of the AMA-negative ones, nor in normal controls or in controls with unrelated liver diseases. sCTLA-4 presence was associated with autoantibodies against MIT3, but not with nuclear autoantibodies (sp100, gp210). This is the first study to demonstrate that levels of sCTLA-4 are elevated in sera of PBC patients. However, they are clearly restricted to patients with AMA positivity, suggesting an immunological difference with respect to AMA-negative ones.

Indexed as

AdultAntigens, NuclearAutoantibodiesAutoantigensCase-Control StudiesCTLA-4 AntigenFemaleHumansLiver Cirrhosis, BiliaryMaleMiddle AgedMitochondriaNuclear Pore Complex ProteinsRecombinant Fusion ProteinsUp-RegulationAntigens, NuclearAutoantibodiesAutoantigensCTLA-4 AntigenCTLA4 protein, humanMIT3 fusion proteinNuclear Pore Complex ProteinsNUP210 protein, humanRecombinant Fusion ProteinsSP100 protein, human

Identifiers

PMID25383768
PMCPMC4226553
OpenAlexW2051724161

What OpenQuestion holds

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LicenceCC BY
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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.