Engineered Extracellular Vesicles/Exosomes as a New Tool against Neurodegenerative Diseases
Open accessAbstract
Neurodegenerative diseases are commonly generated by intracellular accumulation of misfolded/aggregated mutated proteins. These abnormal protein aggregates impair the functions of mitochondria and induce oxidative stress, thereby resulting in neuronal cell death. In turn, neuronal damage induces chronic inflammation and neurodegeneration. Thus, reducing/eliminating these abnormal protein aggregates is a priority for any anti-neurodegenerative therapeutic approach. Although several antibodies against mutated neuronal proteins have been already developed, how to efficiently deliver them inside the target cells remains an unmet issue. Extracellular vesicles/exosomes incorporating intrabodies against the pathogenic products would be a tool for innovative therapeutic approaches. In this review/perspective article, we identify and describe the major molecular targets associated with neurodegenerative diseases, as well as the antibodies already developed against them. Finally, we propose a novel targeting strategy based on the endogenous engineering of extracellular vesicles/exosomes constitutively released by cells of the central nervous system.
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Nefmut loaded into exosomes and fused with a single-chain fragment variable antibody at its C-terminus forms engineered exosomes, proposing a novel targeted strategy for neurodegenerative diseases.
“The researchers loaded Nefmut into exosomes and fused a single-chain fragment variable antibody at its C-terminus to form engineered exosomes, which proposed a novel targeted strategy for endogenous engineering in the treatment of neurodegenerative diseases based on exosomes released by the cellular composition of the CNS [73].”
From The Therapeutic Potential and Clinical Significance of Exosomes as Carriers of Drug Delivery System (2022) · cites this paper as [73]
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References 118 · Cited by 17
Research works printed but not linked: 1
- [63]Caron N.S. Wright G.E. Hayden M.R. Huntington Disease GeneReviews® Adam M.P. Ardinger H.H. Pagon R.A. Wallace S.E. Bean L.J. Stephens K. Amemiya A. University of Washington Seattle, WA, USA 1993 20301482
- Authors
- Ferrantelli, F., Chiozzini, C., Leone, P., Manfredi, F., & Federico, M.
- Affiliations
- Istituto Superiore di Sanità (IT)
- Corresponding author
- Ferrantelli, Flavia
- Federico, Maurizio
- Venue
- Pharmaceutics
- Publisher
- MDPI AG
- Published
- 2020-06-09
- Volume
- 12
- Issue
- 6
- Pages
- 529
- ISSN
- 1999-4923 (ISSN-L)
- PMC
- PMC7357062
- OpenAlex
- W3034234364
- Cited by
- 17
- References
- 118
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 1 · 2021: 4 · 2020: 3
- FWCI
- 0.26
- Type
- journal article
- Language
- en
- Open access
- gold
- dx.doi.org
- Licence
- Locations
- Pharmaceutics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Ministero degli Affari Esteri e della Cooperazione Internazionale (PGR00810)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- engineered extracellular vesicles, exosomes, neurodegenerative diseases, intrabodies, protein aggregation, antibody delivery, central nervous system, oxidative stress, mitochondrial dysfunction, neuroinflammation, neuronal cell death
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