Evidence map›Paper›PMID 31214185›Full record

ReviewFrontiers in immunology2019

The Necrobiology of Mesenchymal Stromal Cells Affects Therapeutic Efficacy.

Daniel J Weiss, Karen English, Anna Krasnodembskaya, Johana M Isaza-Correa, Ian J Hawthorne, Bernard P Mahon

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. The ARDS microenvironment enhances MSC-induced repair via VEGF in experimental acute lung inflammation.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  13. Unraveling the Complexities of Mesenchymal Stromal Cell-based Therapies: One Size Doesn't Fit All.American journal of respiratory and critical care medicine · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Apoptotic MSCs, COX2/PGE2 and clinical efficacy in Crohn fistula.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Daniel J WeissDepartment of Medicine, University of Vermont College of Medicine, Burlington, VT, United States.
Karen EnglishCellular Immunology Laboratory, Biology Department, Human Health Research Institute, Maynooth University, Maynooth, Ireland.
Anna KrasnodembskayaSchool of Medicine, Dentistry and Biomedical Sciences, Wellcome-Wolfson Institute for Experimental Medicine, Queen's University of Belfast, Belfast, United Kingdom.
Johana M Isaza-CorreaImmunology & Cell Biology Laboratory, Biology Department, Human Health Research Institute, Maynooth University, Maynooth, Ireland.
Ian J HawthorneCellular Immunology Laboratory, Biology Department, Human Health Research Institute, Maynooth University, Maynooth, Ireland.
Bernard P MahonImmunology & Cell Biology Laboratory, Biology Department, Human Health Research Institute, Maynooth University, Maynooth, Ireland.
National University of Ireland, Maynooth · IEQueen's University Belfast · GBUniversity of Vermont · US

Funding

Optimizing Functional Recellularization of Acellular Human Lung ScaffoldsR01HL127144 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WEISS, DANIEL J · 2015 to 2018
$1.5M
Decellularized Avian Lungs for Use in Pulmonary TherapeuticsR21EB024329 · NIBIB · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WEISS, DANIEL J · 2017 to 2018
$428k
Medical Research Council MR/R025096/1Medical Research Council MR/S009426/1NHLBI NIH HHS R01 HL127144NIBIB NIH HHS R21 EB024329
6 · The paper itself

Abstract

Rapid progress is occurring in understanding the mechanisms underlying mesenchymal stromal cell (MSC)-based cell therapies (MSCT). However, the results of clinical trials, while demonstrating safety, have been varied in regard to efficacy. Recent data from different groups have shown profound and significant influences of the host inflammatory environment on MSCs delivered systemically or through organ-specific routes, for example intratracheal, with subsequent actions on potential MSC efficacies. Intriguingly in some models, it appears that dead or dying cells or subcellular particles derived from them, may contribute to therapeutic efficacy, at least in some circumstances. Thus, the broad cellular changes that accompany MSC death, autophagy, pre-apoptotic function, or indeed the host response to these processes may be essential to therapeutic efficacy. In this review, we summarize the existing literature concerning the necrobiology of MSCs and the available evidence that MSCs undergo autophagy, apoptosis, transfer mitochondria, or release subcellular particles with effector function in pathologic or inflammatory

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsApoptosisAutophagyBiological TransportCell- and Tissue-Based TherapyCell CommunicationExtracellular VesiclesHumansMacrophagesMesenchymal Stem CellsMitochondriaTreatment Outcomeapoptosisautophagycell therapyefficacyextracellular vesiclesmesenchymal stromal cellmitochondria

Identifiers

PMID31214185
PMCPMC6557974
OpenAlexW2946059227

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.