Evidence map›Paper›PMID 36044737›Full record

ReviewStem cells (Dayton, Ohio)2022

Mesenchymal Stromal/Stem Cell Extracellular Vesicles and Perinatal Injury: One Formula for Many Diseases.

Eleni Delavogia, Dimitrios P Ntentakis, John A Cortinas, Angeles Fernandez-Gonzalez, S Alex Mitsialis, Stella Kourembanas

Open access · greenAbstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

6 authors at 2 institutions in 1 country.

Eleni DelavogiaDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-3363-4854
Dimitrios P NtentakisRetina Service, Angiogenesis Laboratory, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, USA.
John A CortinasDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
Angeles Fernandez-GonzalezDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-1219-9128
S Alex MitsialisDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
Stella KourembanasDivision of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
Boston Children's Hospital · USMassachusetts Eye and Ear Infirmary · US

Funding

MSC Exosome Treatment for BPD: Impact on Immunity and Lung DevelopmentR01HL146128 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI Stella Kourembanas · 2019 to 2026
$6.6M
Mesenchymal Stem Cell Regulation by Syndecan-1 in Lung InjuryR21AI134025 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI KOUREMBANAS, STELLA, PARK, PYONG WOO · 2018 to 2019
$487k
NHLBI NIH HHS R01 HL146128NIAID NIH HHS R21 AI134025
6 · The paper itself

Abstract

Over the past decades, substantial advances in neonatal medical care have increased the survival of extremely premature infants. However, there continues to be significant morbidity associated with preterm birth with common complications including bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), neuronal injury such as intraventricular hemorrhage (IVH) or hypoxic ischemic encephalopathy (HIE), as well as retinopathy of prematurity (ROP). Common developmental immune and inflammatory pathways underlie the pathophysiology of such complications providing the opportunity for multisystem therapeutic approaches. To date, no single therapy has proven to be effective enough to prevent or treat the sequelae of prematurity. In the past decade mesenchymal stem/stromal cell (MSC)-based therapeutic approaches have shown promising results in numerous experimental models of neonatal diseases. It is now accepted that the therapeutic potential of MSCs is comprised of their secretome, and several studies have recognized the small extracellular vesicles (sEVs) as the paracrine vector. Herein, we review the current literature on the MSC-EVs as potential therapeutic agents in neonatal diseases and comment on the progress and challenges of their translation to the clinical setting.

Indexed as

Bronchopulmonary DysplasiaEnterocolitis, NecrotizingExtracellular VesiclesInfant, Newborn, DiseasesMesenchymal Stem CellsPremature BirthFemaleHumansInfantInfant, NewbornPregnancybronchopulmonary dysplasiaextracellular vesiclesmesenchymal stem/stromal cellsMSC-EVsneonatalprematurity

Identifiers

PMID36044737
PMCPMC9707037
OpenAlexW4294125487

What OpenQuestion holds

Textmetadata
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.