Cutting-edge insights into liver fibrosis: advanced therapeutic strategies and future perspectives using engineered mesenchymal stem cell-derived exosomes
Open accessAbstract
Liver fibrosis is still a serious health concern worldwide, and there is increasing interest in mesenchymal stem cells (MSCs) with tremendous potential for treating this disease because of their regenerative and paracrine effects. Recently, many researches have focused on using the released exosomes (EXOs) from stem cells to treat liver fibrosis rather than using parent stem cells themselves. MSC-derived EXOs (MSC-EXOs) have demonstrated favourable outcomes similar to cell treatment in terms of regenerative, immunomodulatory, anti-apoptotic, anti-oxidant, anti-necroptotic, anti-inflammatory and anti-fibrotic actions in several models of liver fibrosis. EXOs are superior to their parent cells in several terms, including lower immunogenicity and risk of tumour formation. However, maintaining the stability and efficacy of EXOs after in vivo transplantation remains a major challenge in their clinical applicability. Therefore, several strategies have been applied in EXOs engineering, such as parental cell modification or modifying EXOs directly to achieve optimum performance of EXOs in treating liver fibrosis. Herein, we discuss the underlying mechanisms of liver fibrosis with an overview of the available therapies, among them EXOs. We also summarise the recent developments in improving the effectiveness of EXOs with the advantages and limitations of these approaches in terms of the upcoming clinical applications.
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Bioengineering or using biomaterials such as hydrogels to deliver EVs may be a potential improvement measure.
“Bioengineering or using biomaterials such as hydrogels to deliver EVs may be a potential improvement measure [198, 259].”
From Mechanisms, efficacy, and future perspectives of cellular-based therapies for liver fibrosis/cirrhosis: focusing on mesenchymal stromal cells (2025) · cites this paper as [198]
The ‘Engineering approaches of EXOs > Cargo loading into EXOs’ section (page unavailable) says surface engineering can improve exosome targeting and therapeutic efficacy, supporting bioengineering as a potential improvement. It also describes a biomaterial used to modify exosome surfaces, but does not describe using hydrogels to deliver EVs; that specific example is unsupported. (LLM, conf=0.85)
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Cited by
Sorted by citations
Pan, X., Gao, T., & Wang, B. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01520-9 · Cited by 2 · see citing works
“Bioengineering or using biomaterials such as hydrogels to deliver EVs may be a potential improvement measure [198, 259].”
- Authors
- Didamoony, M. A., Soubh, A. A., & Ahmed, L. A.
- Affiliations
- Egyptian Russian University (EG)
- Ahram Canadian University (EG)
- Cairo University (EG)
- Corresponding author
- Didamoony, Manar A.
- Ahmed, Lamiaa A.
- Venue
- Drug Delivery and Translational Research
- Published
- 2025-01-24
- Volume
- 15
- Issue
- 8
- Pages
- 2608-2623
- ISSN
- 2190-393X (ISSN-L)
- 2190-3948
- PMC
- PMC12213925
- OpenAlex
- W4406801113
- Cited by
- 9
- References
- 7
- Citations by year
- 2026: 3 · 2025: 6
- FWCI
- 0.80
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Drug Delivery and Translational Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Cairo University
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Keywords
- liver fibrosis, mesenchymal stem cells, exosomes, exosome engineering, stem cell-derived exosomes, exosome stability, immunomodulation, anti-inflammatory activity, antifibrotic therapy, regenerative therapy, clinical translation
- MeSH terms
- Animals, Humans, Liver Cirrhosis, Mesenchymal Stem Cell Transplantation, Exosomes, Mesenchymal Stem Cells
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