Evidence map›Paper›PMID 34527418›Full record

ArticleAging and disease2021

Identification of Molecules Responsible for Therapeutic Effects of Extracellular Vesicles Produced from iPSC-Derived MSCs on Sjo¨gren's Syndrome.

Hyemee Kim, Qingguo Zhao, Heather Barreda, Gagandeep Kaur, Bo Hai, Jong Min Choi, Sung Youn Jung, Fei Liu, Ryang Hwa Lee

Open access · goldAbstract read
In one paragraph

Article in Aging and disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 4 pooled it
2.6field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 4 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  18. Cell therapy in Sjögren's syndrome: opportunities and challenges.Expert reviews in molecular medicine · 2024
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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

9 authors at 1 institution in 1 country.

Hyemee Kim1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Qingguo Zhao1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Heather Barreda1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Gagandeep Kaur1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Bo Hai1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Jong Min Choi2Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Sung Youn Jung2Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Fei Liu1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Ryang Hwa Lee1Department of Molecular and Cellular Medicine, Institute for Regenerative Medicine, College of Medicine, Texas A&M University, College Station, Texas 77845, USA.
Baylor College of Medicine · US

Funding

Extracellular Vesicles Produced by Mesenchymal Stem Cells as Novel Therapy for Autoimmune UveitisR01EY029350 · NEI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LEE, RYANG HWA · 2019 to 2023
$1.8M
Therapeutic effects of MSC-derived extracellular vesicles on Sjögren's SyndromeR21DE027457 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LEE, RYANG HWA, LIU, FEI · 2018 to 2019
$408k
NEI NIH HHS R01 EY029350NIDCR NIH HHS R21 DE027457
6 · The paper itself

Abstract

Recent research indicated that extracellular vesicles (EVs) derived from mesenchymal stem/stromal cells (MSCs) are a promising alternative to MSCs for immunomodulatory therapy. However, the contents of MSC-EVs would change as their parent MSCs change, hence the therapeutic efficacy of MSC-derived EVs (MSC-EVs) would largely depend on donors, tissue sources and culture conditions of MSCs. To overcome limitations of tissue-derived MSCs, we previously used MSCs derived from human induced pluripotent stem cells (iMSCs) to produce EVs and demonstrated their therapeutic potential in a mouse model of secondary Sjo¨gren's Syndrome. Here, we further found that EVs from early-passage iMSCs had better immunomodulatory potency than EVs from late-passage iMSCs in TLR4-stimulated splenocytes and in a mouse model of primary Sjögren's syndrome. Comparative molecular profiling using proteomics and microRNA sequencing revealed distinctive molecular profiles of iMSC-EVs with or without immunomodulation capacity. Amongst them, manipulation of TGF-β1, miR-21 and miR-125b levels in iMSC-EVs significantly affected their immunosuppressive effects. These findings would help improve our understanding of the molecular mechanism underlying iMSC-EV-mediated immunomodulation and further provide strategies to improve regulatory function of EVs for the treatment of immune-mediated diseases.

Indexed as

extracellular vesicles Mesenchymal stem/stromal cellsiPS cellsmolecular profilingsialadenitisSjögren’s syndrome

Identifiers

PMID34527418
PMCPMC8407887
OpenAlexW3198157047

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.