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作为靶向治疗载体的噬菌体:挑战与机遇

Bacteriophages as Targeted Therapeutic Vehicles: Challenges and Opportunities.

作者信息

Venkataraman Srividhya, Shahgolzari Mehdi, Yavari Afagh, Hefferon Kathleen

机构信息

Department of Cell & Systems Biology, University of Toronto, Toronto, ON M5S 3B2, Canada.

Dental Research Center, Avicenna Institute of Clinical Sciences, Avicenna Health Research Institute, Hamadan University of Medical Sciences, Hamadan P.O. Box 6517838678, Iran.

出版信息

Bioengineering (Basel). 2025 Apr 29;12(5):469. doi: 10.3390/bioengineering12050469.

Abstract

Bacteriophages, with their distinctive ability to selectively target host bacteria, stand out as a compelling tool in the realm of drug and gene delivery. Their assembly from proteins and nucleic acids, coupled with their modifiable and biologically unique properties, enables them to serve as efficient and safe delivery systems. Unlike conventional nanocarriers, which face limitations such as non-specific targeting, cytotoxicity, and reduced transfection efficiency in vivo, engineered phages exhibit promising potential to overcome these hurdles and improve delivery outcomes. This review highlights the potential of bacteriophage-based systems as innovative and efficient systems for delivering therapeutic agents. It explores strategies for engineering bacteriophage, categorizes the principal types of phages employed for drug and gene delivery, and evaluates their applications in disease therapy. It provides intriguing details of the use of natural and engineered phages in the therapy of diseases such as cancer, bacterial and viral infections, veterinary diseases, and neurological disorders, as well as the use of phage display technology in generating monoclonal antibodies against various human diseases. Additionally, the use of CRISPR-Cas9 technology in generating genetically engineered phages is elucidated. Furthermore, it provides a critical analysis of the challenges and limitations associated with phage-based delivery systems, offering insights for overcoming these obstacles. By showcasing the advancements in phage engineering and their integration into nanotechnology, this study underscores the potential of bacteriophage-based delivery systems to revolutionize therapeutic approaches and inspire future innovations in medicine.

摘要

噬菌体具有选择性靶向宿主细菌的独特能力,在药物和基因递送领域是一种引人注目的工具。它们由蛋白质和核酸组装而成,再加上其可修饰的生物学独特性质,使其能够作为高效且安全的递送系统。与传统纳米载体不同,传统纳米载体面临诸如非特异性靶向、细胞毒性以及体内转染效率降低等限制,经过工程改造的噬菌体展现出克服这些障碍并改善递送效果的潜力。本综述强调了基于噬菌体的系统作为递送治疗剂的创新高效系统的潜力。它探讨了噬菌体工程改造策略,对用于药物和基因递送的主要噬菌体类型进行了分类,并评估了它们在疾病治疗中的应用。它提供了关于天然和工程改造噬菌体在癌症、细菌和病毒感染、兽医疾病以及神经疾病等疾病治疗中的应用的有趣细节,以及噬菌体展示技术在生成针对各种人类疾病的单克隆抗体方面的应用。此外,还阐明了CRISPR-Cas9技术在生成基因工程噬菌体中的应用。此外,它对基于噬菌体的递送系统相关的挑战和限制进行了批判性分析,为克服这些障碍提供了见解。通过展示噬菌体工程改造的进展及其与纳米技术的整合,本研究强调了基于噬菌体的递送系统革新治疗方法并激发医学未来创新的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ba8/12109052/4ceaeb2e7009/bioengineering-12-00469-g005.jpg

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