Evidence map›Paper›PMID 35885030›Full record

ReviewBiomedicines2022

Adipose-Derived Stem Cell Exosomes as a Novel Anti-Inflammatory Agent and the Current Therapeutic Targets for Rheumatoid Arthritis.

Ting-Hui Chang, Chien-Sheng Wu, Shih-Hwa Chiou, Chih-Hung Chang, Hsiu-Jung Liao

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Investigating theResearch in pharmaceutical sciences · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Exosome-Based Therapeutics in Dermatology.Biomaterials research · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Ting-Hui ChangDepartment of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City 220216, Taiwan.
Chien-Sheng WuDepartment of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City 220216, Taiwan.
Shih-Hwa ChiouDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 100136, Taiwan.
Chih-Hung ChangDepartment of Orthopedic Surgery, Far Eastern Memorial Hospital, New Taipei City 220216, Taiwan.
Hsiu-Jung LiaoDepartment of Medical Research, Far Eastern Memorial Hospital, New Taipei City 220216, Taiwan.ORCID 0000-0002-1763-6537
Far Eastern Memorial Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

FEMH 2022-C-042FEMH 2022-C-123Ministry of Science and Technology Grants 108-2314-B-418-010-MY3Ministry of Science and Technology Grants 109-2314-B-239- 366 001-MY3Ministry of Science and Technology Grants 109-2923-M-010-001-MY3Ministry of Science and Technology Grants 111-2321-B-418-002-NYCU-FEMH Cooperation 109DN24NYCU-FEMH Cooperation 110DN22NYCU-FEMH Cooperation 111DN12NYCU-FEMH Cooperation 111DN22
6 · The paper itself

Abstract

Patients with rheumatoid arthritis (RA), a chronic inflammatory joint disorder, may not respond adequately to current RA treatments. Mesenchymal stem cells (MSCs) elicit several immunomodulatory and anti-inflammatory effects and, thus, have therapeutic potential. Specifically, adipose-derived stem cell (ADSC)-based RA therapy may have considerable potency in modulating the immune response, and human adipose tissue is abundant and easy to obtain. Paracrine factors, such as exosomes (Exos), contribute to ADSCs' immunomodulatory function. ADSC-Exo-based treatment can reproduce ADSCs' immunomodulatory function and overcome the limitations of traditional cell therapy. ADSC-Exos combined with current drug therapies may provide improved therapeutic effects. Using ADSC-Exos, instead of ADSCs, to treat RA may be a promising cell-free treatment strategy. This review summarizes the current knowledge of medical therapies, ADSC-based therapy, and ADSC-Exos for RA and discusses the anti-inflammatory properties of ADSCs and ADSC-Exos. Finally, this review highlights the expanding role and potential immunomodulatory activity of ADSC-Exos in patients with RA.

Indexed as

adipose-derived stem cellanti-inflammationexosomerheumatoid arthritis

Identifiers

PMID35885030
PMCPMC9312519
OpenAlexW4285800087

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.