Evidence map›Paper›PMID 36052734›Full record

ArticleJournal of cellular and molecular medicine2022

Impaired repair properties of endothelial colony-forming cells in patients with granulomatosis with polyangiitis.

Ana Paula Toledo Del Rio, Jéssica O Frade-Guanaes, Stephanie Ospina-Prieto, Bruno K L Duarte, Manoel Barros Bertolo, Margareth C Ozelo, Zoraida Sachetto

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. 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
–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

2 citing papers in PubMed.

  1. Endothelial Progenitor Cells in Autoimmune Disorders.Stem cell reviews and reports · 2023
    Review
  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

7 authors.

Ana Paula Toledo Del RioRheumatology Discipline, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0002-2874-0268
Jéssica O Frade-GuanaesHemocentro UNICAMP, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0003-1008-4458
Stephanie Ospina-PrietoHemocentro UNICAMP, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.
Bruno K L DuarteHemocentro UNICAMP, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0002-6155-3253
Manoel Barros BertoloRheumatology Discipline, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0002-0254-4330
Margareth C OzeloHemocentro UNICAMP, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0001-5938-0675
Zoraida SachettoRheumatology Discipline, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.ORCID 0000-0003-1216-9690

Funding

São Paulo Research Foundation (Fundação de Amparo à Pesquisa do Estado de São Paulo, FAPESP) grant2014/00984-3This research was funded by the Coordination for the Improvement of Higher Education Personnel-Brazil (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, CAPES) FinancingCode001
6 · The paper itself

Abstract

In patients with ANCA-associated vasculitis, interactions between neutrophils and endothelial cells cause endothelial damage and imbalance. Endothelial colony-forming cells (ECFCs) represent a cellular population of the endothelial lineage with proliferative capacity and vasoreparative properties. This study aimed to evaluate the angiogenic capacity of ECFCs of patients with granulomatosis with polyangiitis (GPA). The ECFCs of 13 patients with PR3-positive GPA and 14 healthy controls were isolated and characterized using fluorescence-activated cell sorting, capillary tube formation measurement, scratching assays and migration assays with and without plasma stimulation. Furthermore, three patients with active disease underwent post-treatment recollection of ECFCs for longitudinal evaluation. The ECFCs from the patients and controls showed similar capillary structure formation. However, the ECFCs from the patients with inactive GPA exhibited early losses of angiogenic capacity. Impairments in the migration capacities of the ECFCs were also observed in patients with GPA and controls (12th h, p = 0.05). Incubation of ECFCs from patients with GPA in remission with plasma from healthy controls significantly decreased migration capacity (p = 0.0001). Longitudinal analysis revealed that treatment significantly lowered ECFC migration rates. This study revealed that ECFCs from the patients with PR3-positive GPA in remission demonstrated early losses of tube formation and reduced migration capacity compared to those of the healthy controls, suggesting impairment of endothelial function.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisGranulomatosis with PolyangiitisCells, CulturedEndothelial CellsHumansanti-neutrophil cytoplasmic antibody-associated vasculitisendothelial colony-forming cellsendothelial progenitor cellsgranulomatosis with polyangiitis

Identifiers

PMID36052734
PMCPMC9549508

What OpenQuestion holds

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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.