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Engineered exosomes: a potential therapeutic strategy for septic cardiomyopathy.

Authors :
Mao L
Liu S
Chen Y
Huang H
Ding F
Deng L
Source :
Frontiers in cardiovascular medicine [Front Cardiovasc Med] 2024 Jun 28; Vol. 11, pp. 1399738. Date of Electronic Publication: 2024 Jun 28 (Print Publication: 2024).
Publication Year :
2024

Abstract

Septic cardiomyopathy, a life-threatening complication of sepsis, can cause acute heart failure and carry a high mortality risk. Current treatments have limitations. Fortunately, engineered exosomes, created through bioengineering technology, may represent a potential new treatment method. These exosomes can both diagnose and treat septic cardiomyopathy, playing a crucial role in its development and progression. This article examines the strategies for using engineered exosomes to protect cardiac function and treat septic cardiomyopathy. It covers three innovative aspects: exosome surface modification technology, the use of exosomes as a multifunctional drug delivery platform, and plant exosome-like nanoparticle carriers. The article highlights the ability of exosomes to deliver small molecules, proteins, and drugs, summarizing several RNA molecules, proteins, and drugs beneficial for treating septic cardiomyopathy. Although engineered exosomes are a promising biotherapeutic carrier, they face challenges in clinical application, such as understanding the interaction mechanism with host cells, distribution within the body, metabolism, and long-term safety. Further research is essential, but engineered exosomes hold promise as an effective treatment for septic cardiomyopathy.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (© 2024 Mao, Liu, Chen, Huang, Ding and Deng.)

Details

Language :
English
ISSN :
2297-055X
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in cardiovascular medicine
Publication Type :
Academic Journal
Accession number :
39006168
Full Text :
https://doi.org/10.3389/fcvm.2024.1399738