Evidence map›Paper›PMID 27310015›Full record

ArticlePloS one2016

Remyelination Is Correlated with Regulatory T Cell Induction Following Human Embryoid Body-Derived Neural Precursor Cell Transplantation in a Viral Model of Multiple Sclerosis.

Warren C Plaisted, Angel Zavala, Edna Hingco, Ha Tran, Ronald Coleman, Thomas E Lane, Jeanne F Loring, Craig M Walsh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Brain regulatory T cells.Nature reviews. Immunology · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Neurologic Manifestations of COVID-19.Advances in experimental medicine and biology · 2021
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Promoting remyelination through cell transplantation therapies in a model of viral-induced neurodegenerative disease.Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Review
  17. Article
  18. Article
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Warren C PlaistedDepartment of Molecular Biology & Biochemistry, Sue and Bill Gross Stem Cell Center, Multiple Sclerosis Research Center, Institute for Immunology, University of California Irvine, Irvine, California, United States of America.
Angel ZavalaDepartment of Molecular Biology & Biochemistry, Sue and Bill Gross Stem Cell Center, Multiple Sclerosis Research Center, Institute for Immunology, University of California Irvine, Irvine, California, United States of America.
Edna HingcoDepartment of Molecular Biology & Biochemistry, Sue and Bill Gross Stem Cell Center, Multiple Sclerosis Research Center, Institute for Immunology, University of California Irvine, Irvine, California, United States of America.
Ha TranCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, United States of America.
Ronald ColemanCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, United States of America.
Thomas E LaneDepartment of Pathology, University of Utah, School of Medicine, Salt Lake City, Utah, United States of America.
Jeanne F LoringCenter for Regenerative Medicine, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California, United States of America.
Craig M WalshDepartment of Molecular Biology & Biochemistry, Sue and Bill Gross Stem Cell Center, Multiple Sclerosis Research Center, Institute for Immunology, University of California Irvine, Irvine, California, United States of America.
University of California, Irvine · USScripps Research Institute · USUniversity of Utah · US

Funding

Training Program in Stem Cell Translational Medicine for Neurological DisordersT32NS082174 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PETER John DONOVAN, Leslie Michels Thompson · 2013 to 2026
$3.3M
Human neural precursor cell-mediated therapy in a viral model of demyelinationR01NS092042 · NINDS · UNIVERSITY OF UTAH · PI LANE, THOMAS E, LORING, JEANNE F · 2015 to 2019
$2.8M
NINDS NIH HHS R01 NS092042NINDS NIH HHS T32 NS082174
6 · The paper itself

Abstract

We have recently described sustained clinical recovery associated with dampened neuroinflammation and remyelination following transplantation of neural precursor cells (NPCs) derived from human embryonic stem cells (hESCs) in a viral model of the human demyelinating disease multiple sclerosis. The hNPCs used in that study were derived by a novel direct differentiation method (direct differentiation, DD-NPCs) that resulted in a unique gene expression pattern when compared to hNPCs derived by conventional methods. Since the therapeutic potential of human NPCs may differ greatly depending on the method of derivation and culture, we wanted to determine whether NPCs differentiated using conventional methods would be similarly effective in improving clinical outcome under neuroinflammatory demyelinating conditions. For the current study, we utilized hNPCs differentiated from a human induced pluripotent cell line via an embryoid body intermediate stage (EB-NPCs). Intraspinal transplantation of EB-NPCs into mice infected with the neurotropic JHM strain of mouse hepatitis virus (JHMV) resulted in decreased accumulation of CD4+ T cells in the central nervous system that was concomitant with reduced demyelination at the site of injection. Dampened neuroinflammation and remyelination was correlated with a transient increase in CD4+FOXP3+ regulatory T cells (Tregs) concentrated within the peripheral lymphatics. However, compared to our earlier study, pathological improvements were modest and did not result in significant clinical recovery. We conclude that the genetic signature of NPCs is critical to their effectiveness in this model of viral-induced neurologic disease. These comparisons will be useful for understanding what factors are critical for the sustained clinical improvement.

Indexed as

AnimalsBiomarkersCD4 AntigensCell- and Tissue-Based TherapyCell DifferentiationCoronavirus InfectionsDisease Models, AnimalEmbryoid BodiesForkhead Transcription FactorsGene ExpressionHepatitis, Viral, AnimalHuman Embryonic Stem CellsHumansLymphocyte ActivationMaleMiceBiomarkersCD4 AntigensForkhead Transcription FactorsFoxp3 protein, mouse

Identifiers

PMID27310015
PMCPMC4911106
OpenAlexW2441138583

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.