Evidence map›Paper›PMID 29892282›Full record

ArticleFrontiers in immunology2018

MIS416 Enhances Therapeutic Functions of Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Against Experimental Colitis by Modulating Systemic Immune Milieu.

Byung-Chul Lee, Nari Shin, Jin Young Lee, Insung Kang, Jae-Jun Kim, Seung Eun Lee, Soon Won Choi, Gill A Webster, Kyung-Sun Kang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

9 authors.

Byung-Chul LeeAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Nari ShinAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Jin Young LeeAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Insung KangAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Jae-Jun KimAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Seung Eun LeeAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Soon Won ChoiAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.
Gill A WebsterInnate Therapeutics Ltd., AMSC, Auckland, New Zealand.
Kyung-Sun KangAdult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human adult stem cells, including umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs), have recently been considered a promising alternative treatment for inflammatory bowel disease (IBD) due to their unique immunomodulatory properties and ability to promote tissue regeneration. However, despite many years of research and pre-clinical studies, results from clinical trials using these cells have been diverse and conflicting. This discrepancy is caused by several factors, such as poor engraftment, low survival rate, and donor-dependent variation of the cells. Enhancement of consistency and efficacy of MSCs remains a challenge for the feasibility of cell-based therapy. In this study, we investigated whether administration of MIS416, a novel microparticle that activates NOD2 and TLR9 signaling, could enhance the therapeutic efficacy of hUCB-MSCs against Crohn's disease, using dextran sulfate sodium (DSS)-induced colitis model. Colitis was experimentally induced in mice by using 3% DSS, and mice were administered a retro-orbital injection of MIS416 and subsequent intraperitoneal injection of hUCB-MSCs. Mice were examined grossly, and blood, spleen, and colon tissues were subsequently collected for further

Indexed as

ImmunomodulationMesenchymal Stem Cell TransplantationAnimalsCancer VaccinesCell CycleCell MovementCellular MicroenvironmentChemokine CCL2ColitisCytokinesDextran SulfateDisease Models, AnimalFetal BloodHumansImmunity, InnateMacrophage ActivationCancer VaccinesChemokine CCL2CytokinesDextran SulfateMIS416 vaccineimmune modulatorimmunosuppressioninflammatory bowel diseasesmigration capacityNOD2 and TLR9 signalingstem cell therapy

Identifiers

PMID29892282
PMCPMC5985498

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Registered trials

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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.