Evidence map›Paper›PMID 32266268›Full record

ArticleFrontiers in cell and developmental biology2020

Mesenchymal Stem Cell Derived Extracellular Vesicles Ameliorate Kidney Injury in Aristolochic Acid Nephropathy.

Sharad Kholia, Maria Beatriz Herrera Sanchez, Massimo Cedrino, Elli Papadimitriou, Marta Tapparo, Maria Chiara Deregibus, Stefania Bruno, Federica Antico, Maria Felice Brizzi, Peter J Quesenberry and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Biomimetic materials for medical applications.Chinese medical journal · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Therapeutic application of extracellular vesicles in human diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Overview of aristolochic acid nephropathy: an update.Kidney research and clinical practice · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Extracellular vesicles derived from patients with antibody-mediated rejection induce tubular senescence and endothelial to mesenchymal transition in renal cells.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  20. Extracellular vesicles in kidney disease.Nature reviews. Nephrology · 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

11 authors at 2 institutions in 2 countries.

Sharad KholiaDepartment of Medical Sciences, University of Turin, Turin, Italy.
Maria Beatriz Herrera SanchezMolecular Biotechnology Center, University of Turin, Turin, Italy.
Massimo CedrinoMolecular Biotechnology Center, University of Turin, Turin, Italy.
Elli PapadimitriouMolecular Biotechnology Center, University of Turin, Turin, Italy.
Marta TapparoDepartment of Medical Sciences, University of Turin, Turin, Italy.
Maria Chiara DeregibusMolecular Biotechnology Center, University of Turin, Turin, Italy.
Stefania BrunoDepartment of Medical Sciences, University of Turin, Turin, Italy.
Federica AnticoFORB, Molecular Biotechnology Centre, University of Turin, Turin, Italy.
Maria Felice BrizziDepartment of Medical Sciences, University of Turin, Turin, Italy.
Peter J QuesenberryDivision of Hematology/Oncology, Rhode Island Hospital, Brown University, Providence, RI, United States.
Giovanni CamussiDepartment of Medical Sciences, University of Turin, Turin, Italy.
University of Turin · ITBrown University · US

Funding

Regulation of renal and bone marrow injury by extracellular vesicle non-coding RNUH3TR000880 · NCATS · RHODE ISLAND HOSPITAL · PI QUESENBERRY, PETER J. · 2015 to 2017
$1.1M
Regulation of renal and bone marrow injury by extracellular vesicle non-coding RNUH2TR000880 · NCATS · RHODE ISLAND HOSPITAL · PI QUESENBERRY, PETER J. · 2013 to 2014
$498k
NCATS NIH HHS UH2 TR000880NCATS NIH HHS UH3 TR000880
6 · The paper itself

Abstract

Limitations in the current therapeutic strategies for the prevention of progression of chronic kidney disease (CKD) to end stage renal disease has been a drawback to improving patient recovery. It is therefore imperative that a solution is found to alleviate this problem and improve the health and well-being of patients overall. Aristolochic acid (AA) induced nephropathy, a type of nephrotoxic CKD is characterised by cortical tubular injury, inflammation, leading to interstitial fibrosis. Extracellular vesicles derived from human bone marrow mesenchymal stem cells (MSC-EVs) display therapeutic properties in various disease models including kidney injury. In the current study, we intended to investigate the ability of MSC-EVs on ameliorating tubular injury and interstitial fibrosis in a mouse model of aristolochic acid nephropathy (AAN). The chronic model of AAN is comprised of an intraperitoneal injection of AA in NSG mice, followed by a three-day incubation period and then inoculation of MSC-EVs intravenously. This routine was performed on a weekly basis for four consecutive weeks, accompanied by the monitoring of body weight of all mice. Blood and tissue samples were collected post sacrifice. All animals administered with AA developed kidney injury and renal fibrosis. A gradual loss of body weight was observed, together with a deterioration in kidney function. Although no significant recovery was observed in weight loss following treatment with MSC-EVs, a significant reduction in: blood creatinine and blood urea nitrogen (BUN), tubular necrosis, and interstitial fibrosis was observed. In addition, infiltration of CD45 positive immune cells, fibroblasts, and pericytes which were elevated in the interstitium post AA induced injury, were also significantly reduced by MSC-EVs. Kidneys were also subjected to molecular analyses to evaluate the regulation of pro-fibrotic genes. MSC-EVs significantly reduced AA induction of the pro-fibrotic genes α

Indexed as

aristolochic acid nephropathychronic kidney diseaseextracellular vesiclesfibrosismesenchymal stem cellsmiRNA

Identifiers

PMID32266268
PMCPMC7105599
OpenAlexW3012571543

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.