Evidence map›Paper›PMID 33997712›Full record

ArticleiScience2021

Adipose-mesenchymal stromal cells suppress experimental Sjögren syndrome by IL-33-driven expansion of ST2

Ousheng Liu, Junji Xu, Fu Wang, Wenwen Jin, Peter Zanvit, Dandan Wang, Nathan Goldberg, Alexander Cain, Nancy Guo, Yichen Han and 5 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. The Involvement of Alarmins in the Pathogenesis of Sjögren's Syndrome.International journal of molecular sciences · 2022
    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

15 authors at 4 institutions in 2 countries.

Ousheng LiuMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Junji XuMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Fu WangMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Wenwen JinMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Peter ZanvitMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Dandan WangMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Nathan GoldbergMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Alexander CainMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Nancy GuoMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Yichen HanMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Andrew BynumMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
Guowu MaDalian Medical University, School of Stomatology, Dalian 116044, China.
Songlin WangMolecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, Beijing 100050, China.
Zhangui TangHunan Key Laboratory of Oral Health Research & Hunan 3D Printing Engineering Research Center of Oral Care & Hunan Clinical Research Center of Oral Major Diseases and Oral Health & Xiangya Stomatological Hospital & Xiangya School of Stomatology, Central South University, Changsha 410008, China.
Wanjun ChenMucosal Immunology Section, NIDCR, NIH, Bethesda, MD 20892, USA.
National Institute of Dental and Craniofacial Research · USCapital Medical University · CNCentral South University · CNDalian Medical University · CN

Funding

TGF-beta Regulation of Mucosal and Systemic T Cell Immunity and ToleranceZIADE000101 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI CHEN, WANJUN · 2009 to 2025
$36.9M
Immunotherapy of inflammation, autoimmune disease and cancer ZIADE000737 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI CHEN, WANJUN · 2021 to 2025
$3.8M
6 · The paper itself

Abstract

Adipose-derived mesenchymal stromal cells (ADSCs) play important roles in the alleviation of inflammation and autoimmune diseases. Interleukin-33 (IL-33), a member of the IL-1 family, has been shown to regulate innate and adaptive immunity. However, it is still unknown whether ADSCs regulate immune responses via IL-33. We show here that ADSCs produced IL-33 in response to IL-1β stimulation, which depended on TAK1, ERK, and p38 pathways. ADSCs-derived IL-33 drove the proliferation of CD4

Indexed as

Cell BiologyImmunology

Identifiers

PMID33997712
PMCPMC8105666
OpenAlexW3154606485

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.