Evidence map›Paper›PMID 24818126›Full record

ArticleBioMed research international2014

Association of immunological cell profiles with specific clinical phenotypes of scleroderma disease.

José Manuel López-Cacho, Soledad Gallardo, Manuel Posada, Miriam Aguerri, David Calzada, Teodoro Mayayo, María Luisa González-Rodríguez, Antonio María Rabasco, Carlos Lahoz, Blanca Cárdaba

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

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  14. Innate Immunity in Systemic Sclerosis.Current rheumatology reports · 2017
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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

10 authors at 4 institutions in 1 country.

José Manuel López-CachoDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain.ORCID 0000-0002-9286-8469
Soledad GallardoDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain.ORCID 0000-0002-4046-1130
Manuel PosadaInstitute of Rare Diseases Research, Carlos III Institute of Health, EuroBioBank, and CIBERER, 28029 Madrid, Spain.ORCID 0000-0002-8372-4180
Miriam AguerriDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain.ORCID 0000-0003-2996-2150
David CalzadaDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain.
Teodoro MayayoSani-Red S.L, Barcelona Scientific Park, 08013 Barcelona, Spain.
María Luisa González-RodríguezDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Antonio María RabascoDepartment of Pharmaceutical Technology, Faculty of Pharmacy, University of Seville, 41012 Seville, Spain.
Carlos LahozDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain ; CIBER of Respiratory Diseases (CIBERES), 28029 Madrid, Spain.
Blanca CárdabaDepartment of Immunology, IIS-Jiménez Díaz Foundation, Reyes Católicos Avenue 2, 28040 Madrid, Spain ; CIBER of Respiratory Diseases (CIBERES), 28029 Madrid, Spain.ORCID 0000-0003-0142-9901
Hospital Universitario Fundación Jiménez Díaz · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESUniversidad de Sevilla · ESCentre for Biomedical Network Research on Rare Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to search the correlation among immunological profiles and clinical phenotypes of scleroderma in well-characterized groups of scleroderma patients, comparing forty-nine scleroderma patients stratified according to specific clinical phenotypes with forty-nine healthy controls. Five immunological cell subpopulations (B, CD4(+) and CD8(+) T-cells, NK, and monocytes) and their respective stages of apoptosis and activation were analyzed by flow cytometry, in samples of peripheral blood mononuclear cells (PBMCs). Analyses of results were stratified according to disease stage, time since the diagnosis, and visceral damage (pulmonary fibrosis, pulmonary hypertension, and cardiac affliction) and by time of treatment with corticosteroids. An increase in the percentages of monocytes and a decrease in the B cells were mainly related to the disease progression. A general apoptosis decrease was found in all phenotypes studied, except in localized scleroderma. An increase of B and NK cells activation was found in patients diagnosed more than 10 years ago. Specific cell populations like monocytes, NK, and B cells were associated with the type of affected organ. This study shows how, in a heterogeneous disease, proper patient's stratification according to clinical phenotypes allows finding specific cellular profiles. Our data may lead to improvements in the knowledge of prognosis factors and to aid in the analysis of future specific therapies.

Indexed as

B-LymphocytesFemaleFlow CytometryHumansHypertension, PulmonaryKiller Cells, NaturalLymphocytesMaleMiddle AgedPhenotypePulmonary FibrosisScleroderma, Systemic

Identifiers

PMID24818126
PMCPMC4004116
OpenAlexW1989963870

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.