Evidence map›Paper›PMID 33798448›Full record

ArticleStem cell reports2021

Autophagy-Mediated Activation of Mucosal-Associated Invariant T Cells Driven by Mesenchymal Stem Cell-Derived IL-15.

Guiwen Ye, Peng Wang, Zhongyu Xie, Qian Cao, Jinteng Li, Guan Zheng, Shan Wang, Ming Li, Wenjie Liu, Shuizhong Cen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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

14 authors at 1 institution in 1 country.

Guiwen YeDepartment of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, P.R. China.
Peng WangDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Zhongyu XieDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Qian CaoCenter for Biotherapy, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Jinteng LiDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Guan ZhengDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Shan WangCenter for Biotherapy, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Ming LiDepartment of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, P.R. China.
Wenjie LiuDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Shuizhong CenDepartment of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, P.R. China.
Zhaofeng LiDepartment of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, P.R. China.
Wenhui YuDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China.
Yanfeng WuCenter for Biotherapy, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China. Electronic address: wuyf@mail.sysu.edu.cn.
Huiyong ShenDepartment of Orthopedics, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, P.R. China; Department of Orthopedics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, P.R. China. Electronic address: shenhuiy@mail.sysu.edu.cn.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucosal-associated invariant T (MAIT) cells are innate-like unconventional T cells that are abundant in humans and have attracted increasing attention in recent years. Mesenchymal stem cells (MSCs) are crucial regulators of immune cells. However, whether MAIT cells are regulated by MSCs is unclear. Here, we explored the effect of MSCs on MAIT cells and revealed the underlying mechanism. We found that MSCs did not influence the proliferation of MAIT cells but strikingly induced an activated phenotype with an increased expression of CD69, TNF-α, IFN-γ, and granzyme B. Moreover, MSCs activated MAIT cells in a TCR-MR1-independent mechanism through MSC-secreted IL-15. We revealed that MSC-derived IL-15 activated MAIT cells by enhancing autophagy activity, which was abolished by the autophagy inhibitor 3-methyladenine. Based on our findings, MAIT cells are activated by MSCs through IL-15-induced autophagy, which may help elucidate the mechanisms underlying some immune responses and diseases and provide guidance for future research.

Indexed as

AutophagyCell ProliferationHistocompatibility Antigens Class IHumansInterleukin-15Mesenchymal Stem CellsMinor Histocompatibility AntigensMucosal-Associated Invariant T CellsReceptors, Antigen, T-CellHistocompatibility Antigens Class IInterleukin-15Minor Histocompatibility AntigensMR1 protein, humanReceptors, Antigen, T-Cellautophagyinterleukin-15mesenchymal stem cellsmucosal-associated invariant T cell

Identifiers

PMID33798448
PMCPMC8072065
OpenAlexW3141080251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.