Evidence map›Paper›PMID 39872532›Full record

ArticleFrontiers in immunology2024

The bronchoalveolar lavage fluid

Magda Suchankova, Eszter Zsemlye, Jan Urban, Peter Baráth, Lenka Kohútová, Barbara Siváková, Martina Ganovska, Elena Tibenska, Kinga Szaboova, Eva Tedlova and 8 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

18 authors.

Magda SuchankovaLaboratory of Molecular Immunology, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia.
Eszter ZsemlyeLaboratory of Molecular Immunology, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia.
Jan UrbanNational Institute for Tuberculosis, Lung Diseases and Thoracic Surgery, Vysne Hagy, Slovakia.
Peter BaráthDepartment of Glycobiology, Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia.
Lenka KohútováDepartment of Glycobiology, Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia.
Barbara SivákováDepartment of Glycobiology, Institute of Chemistry, Slovak Academy of Sciences, Bratislava, Slovakia.
Martina GanovskaNational Institute for Tuberculosis, Lung Diseases and Thoracic Surgery, Vysne Hagy, Slovakia.
Elena TibenskaMedirex Ltd., Medirex Group Academy n.p.o., Bratislava, Slovakia.
Kinga SzaboovaMedirex Ltd., Medirex Group Academy n.p.o., Bratislava, Slovakia.
Eva TedlovaDepartment of Pneumology and Phthisiology, Faculty of Medicine Comenius University and University Hospital, Bratislava, Slovakia.
Dominik JuskanicJessenius Diagnostic Center, Nitra, Slovakia.
Kristina KluckovaClinic for Children and Adolescents, Faculty Hospital Nitra, Nitra, Slovakia.
Michaela KardohelyovaInstitute of Immunology, Faculty of Medicine Comenius University, Bratislava, Slovakia.
Tetiana MoskaletsLaboratory of Molecular Immunology, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia.
Anna Ohradanova-RepicMolecular Immunology Unit, Institute for Hygiene and Applied Immunology, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Patrik BabulicLaboratory of Molecular Immunology, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia.
Maria BucovaInstitute of Immunology, Faculty of Medicine Comenius University, Bratislava, Slovakia.
Vladimir LeksaLaboratory of Molecular Immunology, Institute of Molecular Biology, Slovak Academy of Sciences, Bratislava, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Diffuse parenchymal lung diseases (DPLD) cover heterogeneous types of lung disorders. Among many pathological phenotypes, pulmonary fibrosis is the most devastating and represents a characteristic sign of idiopathic pulmonary fibrosis (IPF). Despite a poor prognosis brought by pulmonary fibrosis, there are no specific diagnostic biomarkers for the initial development of this fatal condition. The major hallmark of lung fibrosis is uncontrolled activation of lung fibroblasts to myofibroblasts associated with extracellular matrix deposition and the loss of both lung structure and function. Methods: Here, we used this peculiar feature in order to identify specific biomarkers of pulmonary fibrosis in bronchoalveolar lavage fluids (BALF). The primary MRC-5 human fibroblasts were activated with BALF collected from patients with clinically diagnosed lung fibrosis; the activated fibroblasts were then washed rigorously, and further incubated to allow secretion. Afterwards, the secretomes were analysed by mass spectrometry. Results: In this way, the

Indexed as

Bronchoalveolar Lavage FluidHyaluronan ReceptorsIdiopathic Pulmonary FibrosisLung Diseases, InterstitialPulmonary FibrosisAgedBiomarkersCell LineExosomesFemaleFibroblastsHumansMaleMiddle AgedBiomarkersCD44 protein, humanHyaluronan Receptorsbronchoalveolar lavage fluidsCD44diffuse parenchymal lung diseasesexosomespulmonary fibrosis

Identifiers

PMID39872532
PMCPMC11769834

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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.