# Mesenchymal stem cell-derived extracellular vesicles: emerging cell-free therapeutics for kidney diseases

**Authors:** Si-Jie Chen, Tao-Tao Tang, Yi-Lin Zhang, Lin-Li Lv, Bi-Cheng Liu

PMC · DOI: 10.3389/fimmu.2026.1738491 · Frontiers in Immunology · 2026-03-04

## TL;DR

Mesenchymal stem cell-derived extracellular vesicles show promise as cell-free treatments for kidney diseases due to their regenerative and drug delivery capabilities.

## Contribution

This review systematically summarizes the mechanisms and therapeutic potential of MSC-EVs in kidney diseases.

## Key findings

- MSC-EVs have intrinsic therapeutic effects via their cargo that regulate inflammation and promote cell repair.
- MSC-EVs serve as biocompatible vehicles for drug delivery in kidney disease treatment.
- Ongoing progress suggests MSC-EVs could become next-generation therapies despite standardization challenges.

## Abstract

The increasing global impact of kidney diseases highlights a pressing and unmet need for new treatment strategies. In this context, mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) have emerged as a promising cell-free therapeutic approach, attracting growing interest due to their dual regenerative functions. MSC-EVs not only possess intrinsic therapeutic effects mediated by their cargo of mRNAs, proteins, and miRNAs that regulate inflammation, promote cell repair, reduce fibrosis, but also serve as highly biocompatible vehicles for drug delivery. This versatility places them at the forefront of a potential shift in how kidney diseases may be treated. In this review, we systematically summarize current knowledge on the mechanisms and therapeutic potential of MSC-EVs in various kidney diseases. Although challenges related to standardization and clinical translation persist, ongoing progress supports the view that MSC-EVs are poised to become key next-generation therapies for kidney diseases.

## Full-text entities

- **Diseases:** kidney diseases (MESH:D007674), fibrosis (MESH:D005355), inflammation (MESH:D007249)

## Full text

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## Figures

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## References

111 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996155/full.md

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Source: https://tomesphere.com/paper/PMC12996155