Evidence map›Paper›PMID 24858930›Full record

ReviewBrain research2014

Mesenchymal stem cells as cellular vectors for pediatric neurological disorders.

Donald G Phinney, Iryna A Isakova

Open access · greenAbstract readReview
In one paragraph

Review in Brain research, 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
2.2field-weighted citation impact, top 13% 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, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. A kaleidoscopic view of extracellular vesicles in lysosomal storage disorders.Extracellular vesicles and circulating nucleic acids · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Mesenchymal Stem Cells: Time to Change the Name!Stem cells translational medicine · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Rapid and Efficient Stable Gene Transfer to Mesenchymal Stromal Cells Using a Modified Foamy Virus Vector.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Article
  14. Article
  15. Neurology--the next 10 years.Nature reviews. Neurology · 2015
    Review
  16. 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

2 authors at 2 institutions in 2 countries.

Donald G PhinneyDepartment of Molecular Therapeutics, The Scripps Research Institute, 130 Scripps Way, A213, Jupiter, FL 33458, USA. Electronic address: dphinney@scripps.edu.
Iryna A IsakovaDivision of Clinical Laboratory Diagnostics, Biology Department, National Dnepropetrovsk University, Dnepropetrovsk, Ukraine.
Oles Honchar Dnipro National University · UAScripps Research Institute · US

Funding

Pre-Clinical Trial of MSC-Based Therapy for CNS DiseaseR01NS052301 · NINDS · TULANE UNIVERSITY OF LOUISIANA · PI PHINNEY, DONALD G · 2007 to 2010
$2.2M
Marrow stromal cells for Lysosomal Disease CNS DefectsR01NS039033 · NINDS · TULANE UNIVERSITY OF LOUISIANA · PI PHINNEY, DONALD G · 2001 to 2007
$1.4M
NINDS NIH HHS R01 NS039033NINDS NIH HHS R01 NS052301
6 · The paper itself

Abstract

Lysosomal storage diseases are a heterogeneous group of hereditary disorders characterized by a deficiency in lysosomal function. Although these disorders differ in their etiology and phenotype those that affect the nervous system generally manifest as a profound deterioration in neurologic function with age. Over the past several decades implementation of various treatment regimens including bone marrow and cord blood cell transplantation, enzyme replacement, and substrate reduction therapy have proved effective for managing some clinical manifestations of these diseases but their ability to ameliorate neurologic complications remains unclear. Consequently, there exists a need to develop alternative therapies that more effectively target the central nervous system. Recently, direct intracranial transplantation of tissue-specific stem and progenitor cells has been explored as a means to reconstitute metabolic deficiencies in the CNS. In this chapter we discuss the merits of bone marrow-derived mesenchymal stem cells (MSCs) for this purpose. Originally identified as progenitors of connective tissue cell lineages, recent findings have revealed several novel aspects of MSC biology that make them attractive as therapeutic agents in the CNS. We relate these advances in MSC biology to their utility as cellular vectors for treating neurologic sequelae associated with pediatric neurologic disorders.

Indexed as

AnimalsBrainChildHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNervous System DiseasesCell therapyCentral nervous systemLysosomal storage diseaseMarrow stromal cellMesenchymal stem cellMigrationParacrine signalingPediatric

Identifiers

PMID24858930
PMCPMC4103155
OpenAlexW2046894975

What OpenQuestion holds

Textmetadata
LicenceTDM
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.