Evidence map›Paper›PMID 33824286›Full record

ArticleCell death & disease2021

Eradication of specific donor-dependent variations of mesenchymal stem cells in immunomodulation to enhance therapeutic values.

Chunxue Zhang, Liqiang Zhou, Zhen Wang, Wenxia Gao, Wei Chen, Huina Zhang, Bo Jing, Xu Zhu, Lei Chen, Changhong Zheng and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. HBEGF/EGFR pathway activation by hUC-MSCs improves cognitive outcomes in anti-NMDAR encephalitis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Unlocking the Therapeutic Code of Mesenchymal Stromal Cells.American journal of respiratory and critical care medicine · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. N-CADHERINStem cell research & therapy · 2024
    Article
  20. 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

15 authors at 3 institutions in 1 country.

Chunxue Zhang *Stem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Liqiang Zhou *Stem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Zhen WangStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Wenxia GaoStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Wei ChenStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Huina ZhangStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Bo JingSchool of Life Science, Southern University of Science and Technology (SUSTech), Shenzhen, 518055, China.
Xu ZhuKey Laboratory of Spine and Spinal Cord Injury Repair and Regeneration (Tongji University), Ministry of Education, Shanghai, 200065, China.
Lei ChenKey Laboratory of Spine and Spinal Cord Injury Repair and Regeneration (Tongji University), Ministry of Education, Shanghai, 200065, China.
Changhong ZhengShanghai Institute of Stem Cell Research and Clinical Translation, Shanghai East Hospital, Tongji University, School of Medicine, Shanghai, 200120, China.
Kaiyan ShiShanghai Institute of Stem Cell Research and Clinical Translation, Shanghai East Hospital, Tongji University, School of Medicine, Shanghai, 200120, China.
Li WuShanghai Institute of Stem Cell Research and Clinical Translation, Shanghai East Hospital, Tongji University, School of Medicine, Shanghai, 200120, China.
Liming ChengStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China.
Kunshan ZhangStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China. zhangkunshan@tongji.edu.cn.ORCID 0000-0003-0562-419X
Yi Eve SunStem Cell Translational Research Center, Tongji Hospital, Tongji University, School of Medicine, Shanghai, 200065, China. yi.eve.sun@gmail.com.
Tongji University · CNShanghai East Hospital · CNSouthern University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are one of the most widely clinically trialed stem cells, due to their abilities to differentiate into multiple cell lineages, to secrete regenerative/rejuvenative factors, and to modulate immune functions, among others. In this study, we analyzed human umbilical-cord-derived MSCs from 32 donors and revealed donor-dependent variations in two non-correlated properties, (1) cell proliferation, and (2) immune modulatory functions in vitro and in vivo, which might explain inconsistent clinical efficacies of MSCs. Through unbiased transcriptomic analyses, we discovered that IFN-γ and NF-κB signaling were positively associated with immune modulatory function of MSCs. Activation of these two pathways via IFN-γ and TNF-α treatment eradicated donor-dependent variations. Additional transcriptomic analyses revealed that treatment with these two factors, while having abolished donor-dependent variations in immune modulatory function, did not overall make different donor-derived MSCs the same at whole transcriptomic levels, demonstrating that the cells were still different in many other biological perspectives, and may not perform equally for therapeutic purposes other than immune modulation. Pre-selection or pre-treatment to eradicate MSC variations in a disease-treatment-specific manner would therefore be necessary to ensure clinical efficacies. Together this study provided novel insights into the quality control perspective of using different-donor-derived MSCs to treat inflammation-related clinical conditions and/or autoimmune diseases.

Indexed as

Autoimmune DiseasesCell ProliferationCells, CulturedHumansImmunomodulationInterferon-gammaMesenchymal Stem CellsMesenchymal Stem Cell TransplantationUmbilical CordInterferon-gamma

Identifiers

PMID33824286
PMCPMC8024246
OpenAlexW3152276990

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.