Evidence map›Paper›PMID 36153571›Full record

ArticleStem cell research & therapy2022

TNFAIP6 defines the MSC subpopulation with enhanced immune suppression activities.

Lingyun Li, Lei Yang, Xian Chen, Xiangjuan Chen, Lianghui Diao, Yong Zeng, Jianyong Xu

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Improved therapeutic consistency and efficacy of CD317Stem cell research & therapy · 2024
    Article
  13. CD317Stem cell research & therapy · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. 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

7 authors at 3 institutions in 1 country.

Lingyun Li *Department of Immunology, School of Medicine, Health Science Center, Shenzhen University, Nanhai Avenue 3688, Shenzhen, 518060, Guangdong, People's Republic of China.
Lei Yang *Department of Immunology, School of Medicine, Health Science Center, Shenzhen University, Nanhai Avenue 3688, Shenzhen, 518060, Guangdong, People's Republic of China.
Xian Chen *Shenzhen Key Laboratory for Reproductive Immunology of Peri-Implantation, Shenzhen Zhongshan Institute for Reproduction and Genetics, Fertility Center, Shenzhen Zhongshan Urology Hospital, Shenzhen, 518060, Guangdong, People's Republic of China.
Xiangjuan Chen *Department of Obstetrics, Shenzhen University General Hospital, Shenzhen University, Shenzhen, People's Republic of China.
Lianghui DiaoShenzhen Key Laboratory for Reproductive Immunology of Peri-Implantation, Shenzhen Zhongshan Institute for Reproduction and Genetics, Fertility Center, Shenzhen Zhongshan Urology Hospital, Shenzhen, 518060, Guangdong, People's Republic of China.
Yong ZengShenzhen Key Laboratory for Reproductive Immunology of Peri-Implantation, Shenzhen Zhongshan Institute for Reproduction and Genetics, Fertility Center, Shenzhen Zhongshan Urology Hospital, Shenzhen, 518060, Guangdong, People's Republic of China.
Jianyong XuDepartment of Immunology, School of Medicine, Health Science Center, Shenzhen University, Nanhai Avenue 3688, Shenzhen, 518060, Guangdong, People's Republic of China. xujianyong820915@163.com.ORCID 0000-0003-1910-4603
Shenzhen University Health Science Center · CNShenzhen University · CNShenzhen Zhongshan Urological Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stromal/stem cells (MSCs) have been intensively investigated in both pre-clinical and clinical studies. However, the therapeutic efficacy varies resulting from the heterogenicity of MSCs. Therefore, purifying the specific MSC subpopulation with specialized function is necessary for their therapeutic applications.

methodsThe large-scale RNA sequencing analysis was performed to identify potential cell markers for the mouse MSCs. Then, the immune suppression activities of the purified MSC subpopulation were assessed in vitro and in vivo.

resultsThe TNFAIP6 (tumor necrosis factor alpha-induced protein 6) has been identified as a potential cell marker for mouse MSCs, irrespective of tissue origin and laboratory origin. The TNFAIP6

conclusionsTherefore, we have demonstrated that the TNFAIP6

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsDisease Models, AnimalImmunosuppression TherapyMiceTumor Necrosis Factor-alphaTumor Necrosis Factor-alphaImmune suppressionMesenchymal stromal/stem cellsMSCsTNFAIP6Tumor necrosis factor alpha-induced protein 6

Identifiers

PMID36153571
PMCPMC9509641
OpenAlexW4296946251

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.