Evidence map›Paper›PMID 19191336›Full record

ArticleGlia2009

Human bone marrow-derived mesenchymal stem cells induce Th2-polarized immune response and promote endogenous repair in animal models of multiple sclerosis.

Lianhua Bai, Donald P Lennon, Valerie Eaton, Kari Maier, Arnold I Caplan, Stephen D Miller, Robert H Miller

Abstract read
In one paragraph

Article in Glia, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 236 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
236citing papers in PubMed, 4 pooled it
18.6field-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

236 citing papers in PubMed, 4 syntheses or guidelines pooled it, 538 citations in OpenAlex.

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176 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

7 authors at 2 institutions in 1 country.

Lianhua BaiCase Western Reserve University, Centers for Stem Cells and Regenerative Medicine, Translational Neuroscience, Department of Neurosciences, Case School of Medicine, Cleveland, Ohio 44106, USA.
Donald P Lennon
Valerie Eaton
Kari Maier
Arnold I Caplan
Stephen D Miller
Robert H Miller
Case Western Reserve University · USNorthwestern University · US

Funding

Development of Oligodendrycytes in the Spinal CordR01NS030800 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI MILLER, ROBERT H. · 1995 to 2018
$5.7M
Chemokine Synergy with PDGF Oligodendrocyte PrecursorsR37NS036674 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI MILLER, ROBERT H · 2001 to 2007
$2.6M
CHEMOKINE SYNERGY WITH PDGF--OLIGODENDROCYTE PRECURSORSR01NS036674 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI MILLER, ROBERT H · 1997 to 2000
$201k
NINDS NIH HHS NS-30800NINDS NIH HHS NS-36674NINDS NIH HHS R01 NS030800NINDS NIH HHS R01 NS036674NINDS NIH HHS R37 NS036674
6 · The paper itself

Abstract

Cell-based therapies are attractive approaches to promote myelin repair. Recent studies demonstrated a reduction in disease burden in mice with experimental allergic encephalomyelitis (EAE) treated with mouse mesenchymal stem cells (MSCs). Here, we demonstrated human bone marrow-derived MSCs (BM-hMSCs) promote functional recovery in both chronic and relapsing-remitting models of mouse EAE, traced their migration into the injured CNS and assayed their ability to modulate disease progression and the host immune response. Injected BM-hMSCs accumulated in the CNS, reduced the extent of damage and increased oligodendrocyte lineage cells in lesion areas. The increase in oligodendrocytes in lesions may reflect BM-hMSC-induced changes in neural fate determination, since neurospheres from treated animals gave rise to more oligodendrocytes and less astrocytes than nontreated neurospheres. Host immune responses were also influenced by BM-hMSCs. Inflammatory T-cells including interferon gamma producing Th1 cells and IL-17 producing Th17 inflammatory cells and their associated cytokines were reduced along with concomitant increases in IL-4 producing Th2 cells and anti-inflammatory cytokines. Together, these data suggest that the BM-hMSCs represent a viable option for therapeutic approaches.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBone Marrow CellsBrainCytokinesDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansInterleukin-17Interleukin-4Mesenchymal Stem CellsMiceMice, Inbred C57BLMice, TransgenicMultiple SclerosisCytokinesInterleukin-17Interleukin-4

Identifiers

PMID19191336
PMCPMC2706928
OpenAlexW2154677662

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.