Evidence map›Paper›PMID 40292402›Full record

ReviewInternational journal of nanomedicine2025

Exosomes in Systemic Autoimmune Diseases: Recent Advances in Diagnostic Biomarkers and Therapeutic Applications.

Xinchen Lv, Wendong Liu, Xue Zhou, Yu Yang, Wangqian Zhao, Linfeng Meng, Fenghuoyi Mu, Zhixiang Zhang, Shaohua Zhu, Shuai Zhang and 1 more

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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

11 authors.

Xinchen LvDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.ORCID 0009-0003-3648-0798
Wendong LiuDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Xue ZhouDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Yu YangDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Wangqian ZhaoDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Linfeng MengDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Fenghuoyi MuDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Zhixiang ZhangDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Shaohua ZhuDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Shuai ZhangDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.
Ying WangDepartment of Forensic Medicine, School of Basic Medical Sciences, Soochow University, Suzhou, 215123, People's Republic of China.ORCID 0000-0001-8894-373X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic autoimmune diseases (SADs) encompass a spectrum of organ involvement, clinical heterogeneity, and therapeutic challenges meriting significant research. These conditions involve the immune system mistakenly attacking and damaging multiple body tissues and organs, leading to chronic inflammation and damage. Exosomes are nanoscale extracellular vesicles secreted by cells that modulate intercellular communication and immunity. Accumulating evidence indicates that exosomes have multifaceted roles in the pathogenesis of SADs through processes like cellular signaling, immune modulation, antigen presentation, and inflammatory response. The cargo of exosomes, such as proteins, miRNAs, and lipids, are vital determinants of cellular and humoral immunity. This review examines key signaling pathways in four common SADs, rheumatoid arthritis, systemic lupus erythematosus, systemic sclerosis, and Sjögren's syndrome, and explores exosome as non-invasive biomarkers for diagnosis, disease monitoring, and therapeutic response prediction. Additionally, the therapeutic potential of mesenchymal stromal cells (MSCs) or various type of mesenchymal stem cells derived exosomes as cell-free immunotherapies for SADs is highlighted. Engineered exosomes, with enhanced targeting, bioavailability, low toxicity, are emerging as promising drug delivery vehicles. However, challenges such as high production costs, technical complexity, and inefficiency, along with the lack of standardized protocols, limit clinical implementation in SADs. A deeper understanding of exosome roles in SADs pathogenesis and innovative immunotherapies may provide valuable theoretical support for the diagnosis and treatment of these challenging conditions.

Indexed as

Autoimmune DiseasesExosomesAnimalsArthritis, RheumatoidBiomarkersDrug Delivery SystemsHumansImmunotherapyMesenchymal Stem CellsSignal TransductionBiomarkersbiomarkersexosomesimmunoregulationMSC-therapysystemic autoimmune diseases

Identifiers

PMID40292402
PMCPMC12024484

What OpenQuestion holds

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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.