Evidence map›Paper›PMID 33951487›Full record

ReviewFree radical biology & medicine2021

Recent advances in Extracellular Vesicles and their involvements in vasculitis.

Nan Yang, Yin Zhao, Xiuhua Wu, Na Zhang, Haoming Song, Wei Wei, Ming-Lin Liu

Open access · greenAbstract readReview
In one paragraph

Review in Free radical biology & medicine, 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
1.0field-weighted citation impact, top 26% 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, 12 citations in OpenAlex.

  1. Article
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  6. Exosome to Promote Cancer Progression via Its Bioactive Cargoes.Archives of cancer biology and therapy · 2021
    Article
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

7 authors at 3 institutions in 2 countries.

Nan YangDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300052, PR China.
Yin ZhaoDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300052, PR China.
Xiuhua WuDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300052, PR China.
Na ZhangDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300052, PR China.
Haoming SongDepartment of Cardiology, Tongji Hospital, Tongji University School of Medicine, Shanghai, 200065, PR China.
Wei WeiDepartment of Rheumatology and Immunology, Tianjin Medical University General Hospital, Tianjin, 300052, PR 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 · USTongji University · CN

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

Systemic vasculitis is a heterogeneous group of multisystem autoimmune disorders characterized by inflammation of blood vessels. Although many progresses in diagnosis and immunotherapies have been achieved over the past decades, there are still many unanswered questions about vasculitis from pathological understanding to more advanced therapies. Extracellular vesicles (EVs) are double-layer phospholipid membrane vesicles harboring various cargoes. EVs can be classified into exosomes, microvesicles (MVs), and apoptotic bodies depending on their size and origin of cellular compartment. EVs can be released by almost all cell types and may be involved in physical and pathological processes including inflammation and autoimmune responses. In systemic vasculitis, EVs may have pathogenic involvement in inflammation, autoimmune responses, thrombosis, endothelium injury, angiogenesis and intimal hyperplasia. EV-associated redox reaction may also be involved in vasculitis pathogenesis by inducing inflammation, endothelial injury and thrombosis. Additionally, EVs may serve as specific biomarkers for diagnosis or monitoring of disease activity and therapeutic efficacy, i.e. AAV-associated renal involvement. In this review, we have discussed the recent advances of EVs, especially their roles in pathogenesis and clinical involvements in vasculitis.

Indexed as

Autoimmune DiseasesCell-Derived MicroparticlesExosomesExtracellular VesiclesVasculitisHumansAutoimmunityExtracellular vesiclesInflammationRedoxSystemic vasculitis

Identifiers

PMID33951487
PMCPMC9107955
OpenAlexW3157534999

What OpenQuestion holds

Textmetadata
LicenceTDM
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.