Evidence map›Paper›PMID 33276479›Full record

ArticleBiomedicines2020

TNF-α Priming Elicits Robust Immunomodulatory Potential of Human Tonsil-Derived Mesenchymal Stem Cells to Alleviate Murine Colitis.

Tae-Hoon Shin, Ji-Su Ahn, Su-Jeong Oh, Ye Young Shin, Ji Won Yang, Min-Jung Kang, Ji Min Kim, Byung-Joo Lee, Yoojin Seo, Hyung-Sik Kim

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Roe-inspired stem cell microcapsules for inflammatory bowel disease treatment.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Review
  8. 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

10 authors at 3 institutions in 2 countries.

Tae-Hoon ShinTranslational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Ji-Su AhnDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Su-Jeong OhDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Ye Young ShinDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Ji Won YangDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Min-Jung KangDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Ji Min KimDepartment of Otorhinolaryngology-Head and Neck Surgery, Biomedical Research Institute, Pusan National University School of Medicine, Pusan National University Hospital, Busan 49241, Korea.ORCID 0000-0002-3608-765X
Byung-Joo LeeDepartment of Otorhinolaryngology-Head and Neck Surgery, Biomedical Research Institute, Pusan National University School of Medicine, Pusan National University Hospital, Busan 49241, Korea.ORCID 0000-0001-7091-6688
Yoojin SeoDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.
Hyung-Sik KimDental and Life Science Institute, Pusan National University, Yangsan 50612, Korea.ORCID 0000-0002-7588-7393
Pusan National University · KRPusan National University Hospital · KRNational Institutes of Health · US

Funding

National Research Foundation of Korea NRF-2018R1A5A2023879 and NRF-2017R1E1A1A01074316
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been spotlighted in the field of cell therapies as a promising tool for the treatment of intractable inflammatory diseases. However, their therapeutic potency still shows a gap between preclinical and clinical settings, and distinctive characteristics of specific tissue-derived MSCs and definitive ways to maximize their beneficial functions have not been fully elucidated yet. We previously identified the unique MSCs population from human palatine tonsil (TMSCs) and revealed their superior properties in proliferation and ROS regulation. Based on these findings, we explored further characteristics of TMSCs particularly focused on immunomodulatory function. We found the merit of TMSCs as a therapeutic agent that retains favorable MSCs properties until relatively late passages and revealed that pre-treatment of TNF-α can enhance the immunomodulatory abilities of TMSCs through the upregulation of the PTGS2/PGE

Indexed as

colitiscyclooxygenase-2immunomodulationmesenchymal stem cellpalatine tonsilprostaglandin E2tumor necrosis factor alpha

Identifiers

PMID33276479
PMCPMC7760130
OpenAlexW3107289800

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.