Evidence map›Paper›PMID 41368286›Full record

ReviewInternational journal of nanomedicine2025

Mesenchymal Stem Cell-Derived Exosomes in Anti-NET Therapy: Mechanisms, Challenges, and Future Perspectives.

Yihao Ye, Yushan Ye, Mei Tian, Yitao Zhao, Ziwei Guo, Chenghong Jin, Shiwei Duan, Yueliang Zheng

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

8 authors.

Yihao Ye *The Second School of Clinical Medicine, Hangzhou Normal University, Hangzhou, Zhejiang, 311121, People's Republic of China.
Yushan Ye *Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, People's Republic of China.
Mei TianKey Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, People's Republic of China.
Yitao ZhaoKey Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, People's Republic of China.
Ziwei GuoEmergency and Critical Care Center, Department of Emergency Medicine, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 314408, People's Republic of China.
Chenghong JinKey Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, People's Republic of China.
Shiwei DuanKey Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, People's Republic of China.
Yueliang ZhengEmergency and Critical Care Center, Department of Emergency Medicine, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, 314408, People's Republic of China.ORCID 0000-0002-2152-6031

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils, a key component of the innate immune system, play a crucial role in immune responses. In 2004, Brinkmann et al identified neutrophil extracellular traps (NETs) as a novel antibacterial mechanism. However, NETs have since been implicated in the pathogenesis of various diseases, including autoimmune disorders, sepsis, and cancer. Consequently, targeting NETs has emerged as a promising therapeutic approach. Mesenchymal stem cells (MSCs) have demonstrated efficacy in modulating NET formation, but MSC-derived exosomes offer distinct advantages over whole MSCs due to their lower immunogenicity, higher biological stability, and ability to deliver bioactive molecules like miRNAs and CD59. These exosomes can block critical signaling pathways involved in NET formation and protect neutrophil mitochondria, inhibiting NET release. Despite challenges such as low yield and targeting efficiency, ongoing research has made significant strides in addressing these issues. This article reviews the current progress in MSC-derived exosome-based anti-NET therapies and discusses potential strategies to enhance their therapeutic application.

Indexed as

ExosomesExtracellular TrapsMesenchymal Stem CellsAnimalsHumansMesenchymal Stem Cell TransplantationMicroRNAsNeutrophilsMicroRNAsexosomesMSCMSC-exoneutrophil extracellular trapsneutrophils

Identifiers

PMID41368286
PMCPMC12684992

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.