Evidence map›Paper›PMID 24107995›Full record

ArticleNature2013

A regenerative approach to the treatment of multiple sclerosis.

Vishal A Deshmukh, Virginie Tardif, Costas A Lyssiotis, Chelsea C Green, Bilal Kerman, Hyung Joon Kim, Krishnan Padmanabhan, Jonathan G Swoboda, Insha Ahmad, Toru Kondo and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 286 papers.

0numbers the graph read from it
0cells of the map it votes in
286citing papers in PubMed
18.1field-weighted citation impact, top 1% 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

286 citing papers in PubMed, 510 citations in OpenAlex.

  1. Review
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  13. Repeated ablations of mature Tmem10Cell death & disease · 2025
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  17. Progressive multiple sclerosis: Evaluating current therapies and exploring future treatment strategies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  18. Article
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Vishal A DeshmukhDepartment of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Virginie TardifDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Costas A LyssiotisDepartment of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Chelsea C GreenDepartment of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Bilal KermanLaboratory of Genetics, The Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.
Hyung Joon KimLaboratory of Genetics, The Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.
Krishnan PadmanabhanLaboratory of Genetics, The Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.
Jonathan G SwobodaDepartment of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Insha AhmadDepartment of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Toru KondoDivision of Stem Cell Biology, Institute for Genetic Medicine, Hokkaido University, Kita-15, Nishi- 7, Kita-ku, Sapporo 060-0815, Japan.
Fred H GageLaboratory of Genetics, The Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.
Argyrios N TheofilopoulosDepartment of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Brian R Lawson *Department of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Peter G Schultz *Department of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Luke L Lairson *Department of Chemistry, The Scripps Research Institute, 10550, North Torrey Pines Road, La Jolla, California 92037, USA.
Scripps Research Institute · USSalk Institute for Biological Studies · USCalifornia Institute for Biomedical Research · USHokkaido University · JP

Funding

Genetic Basis of Systemic AutoimmunityR37AR039555 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2003 to 2012
$4.2M
TYPE I INTERFERONS IN LUPUSR01AR053228 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2006 to 2010
$2.0M
ENGRAFTING HUMAN NEURONS INTO ANIMAL MODELS TO STUDY SCHIZOPHRENIAR00MH101634 · NIMH · UNIVERSITY OF ROCHESTER · PI PADMANABHAN, KRISHNAN · 2016 to 2018
$731k
The endosomal SLC15A4 proton-coupled histidine transporter in lupusR21AR065384 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 2013 to 2014
$443k
Engrafting human neurons into animal models to study schizophreniaK99MH101634 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI PADMANABHAN, KRISHNAN · 2013 to 2014
$175k
NIAMS NIH HHS R01 AR053228NIAMS NIH HHS R21 AR065384NIAMS NIH HHS R37 AR039555NIMH NIH HHS K99 MH101634NIMH NIH HHS R00 MH101634
6 · The paper itself

Abstract

Progressive phases of multiple sclerosis are associated with inhibited differentiation of the progenitor cell population that generates the mature oligodendrocytes required for remyelination and disease remission. To identify selective inducers of oligodendrocyte differentiation, we performed an image-based screen for myelin basic protein (MBP) expression using primary rat optic-nerve-derived progenitor cells. Here we show that among the most effective compounds identifed was benztropine, which significantly decreases clinical severity in the experimental autoimmune encephalomyelitis (EAE) model of relapsing-remitting multiple sclerosis when administered alone or in combination with approved immunosuppressive treatments for multiple sclerosis. Evidence from a cuprizone-induced model of demyelination, in vitro and in vivo T-cell assays and EAE adoptive transfer experiments indicated that the observed efficacy of this drug results directly from an enhancement of remyelination rather than immune suppression. Pharmacological studies indicate that benztropine functions by a mechanism that involves direct antagonism of M1 and/or M3 muscarinic receptors. These studies should facilitate the development of effective new therapies for the treatment of multiple sclerosis that complement established immunosuppressive approaches.

Indexed as

Models, BiologicalAnimalsAntiparkinson AgentsBenztropineCell DifferentiationCoculture TechniquesCuprizoneEncephalomyelitis, Autoimmune, ExperimentalFemaleFingolimod HydrochlorideImmune SystemMiceMice, Inbred C57BLMultiple SclerosisMyelin Proteolipid ProteinMyelin SheathAntiparkinson AgentsBenztropineCuprizoneFingolimod HydrochlorideMyelin Proteolipid ProteinPropylene GlycolsReceptor, Muscarinic M1Receptor, Muscarinic M3Sphingosine

Identifiers

PMID24107995
PMCPMC4431622
OpenAlexW2078482008

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.