Evidence map›Paper›PMID 32893081›Full record

ReviewJournal of autoimmunity2020

Extracellular vesicles and lupus nephritis - New insights into pathophysiology and clinical implications.

Yin Zhao, Wei Wei, Ming-Lin Liu

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Journal of autoimmunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04894695 (Identification of Biomarkers for Lupus Nephritis Using Urine Exosomes), which is not on this map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
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.

NCT04894695 unknown statusnot on this map

Identification of Biomarkers for Lupus Nephritis Using Urine Exosomes

TypeobservationalSponsorRenJi HospitalRan2020 to 2021Enrolled400ConditionsLupus NephritisArmsbiomarkers detection in different groups
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Association ofFrontiers in immunology · 2025
    Pooled it
  2. Observational
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Urinary extracellular vesicle RNAs as novelClinical kidney journal · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Extracellular Vesicles as Source of Biomarkers in Glomerulonephritis.International journal of molecular sciences · 2023
    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

3 authors at 2 institutions in 2 countries.

Yin ZhaoDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300020, China.
Wei WeiDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300020, China. Electronic address: tjweiwei2003@163.com.
Ming-Lin LiuDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA; Corporal Michael J. Crescenz VA Medical Center (Philadelphia), Philadelphia, PA, 19104, USA. Electronic address: lium1@pennmedicine.upenn.edu.
Tianjin Medical University General Hospital · CNPhiladelphia VA Medical Center · US

Funding

Extracellular vesicle-associated MAVS and IFNẞ in DermatomyositisR21AI144838 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI LIU, MING-LIN · 2019 to 2020
$443k
NIAID NIH HHS R21 AI144838
6 · The paper itself

Abstract

Lupus nephritis (LN) is a major cause for overall morbidity and mortality in patients with systemic lupus erythematosus (SLE), while its pathogenic mechanisms are still not well understood. Extracellular vesicles (EVs) are membrane vesicles that are released from almost all cell types. EVs can be subdivided into exosomes, microvesicles, and apoptotic bodies. Latest studies have shown that EVs can be released during several cellular events, including cell activation, autophagy, and several types of programed cell death, i.e. apoptosis, necroptosis, pyroptosis, and NETosis. Emerging evidence demonstrates that EVs harbor different bioactive molecules, including nucleic acids, proteins, lipids, cytokines, immune complexes (ICs), complements, and other molecules, some of which may contribute to pathogenesis of autoimmune diseases. EVs can serve as novel information shuttle to mediate local autocrine or paracrine signals to nearby cells, and distant endocrine signals to cells located far away. In LN, EVs may have pathogenic effects by transportation of autoantigens or complements, promotion of IC deposition or complement activation, and stimulation of inflammatory responses, renal tissue injury, or microthrombus formation. Additionally, EVs released from kidney cells may serve as specific biomarkers for diagnosis or monitoring of disease activity and therapeutic efficacy. In this review, we will summarize the latest progress about EV generation from basic research, their potential pathologic effects on LN, and their clinical implications. The cutting-edge knowledge about EV research provides insights into novel therapeutic strategy, new tools for diagnosis or prognosis, and evaluation approaches for treatment effectiveness in LN.

Indexed as

Autocrine CommunicationBiomarkersExtracellular VesiclesHumansKidneyLupus NephritisParacrine CommunicationPrognosisSeverity of Illness IndexBiomarkersAutoantigenExtracellular vesiclesImmune complexInflammationLupus nephritis

Identifiers

PMID32893081
PMCPMC9107953
OpenAlexW3083181989

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.