Engineered bacterial outer membrane vesicles: a versatile bacteria-based weapon against gastrointestinal tumors

被引:13
作者
Zheng, Keshuang [1 ,2 ,3 ,4 ]
Feng, Yongpu [1 ,2 ,3 ,4 ]
Li, Lei [5 ]
Kong, Fanyang [1 ,2 ,3 ,4 ]
Gao, Jie [6 ]
Kong, Xiangyu [1 ,2 ,3 ,4 ,6 ]
机构
[1] Naval Med Univ, Natl Key Lab Immunol & Inflammat, Shanghai 200433, Peoples R China
[2] Naval Med Univ, Inst Neurosci, Key Lab Mol Neurobiol, Minist Educ, Shanghai 200433, Peoples R China
[3] Naval Med Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200433, Peoples R China
[4] Naval Med Univ, Changhai Hosp, Dept Gastroenterol, Shanghai, Peoples R China
[5] Shanghai Tenth Peoples Hosp, Digest Endoscopy Ctr, Shanghai, Peoples R China
[6] Naval Med Univ, Changhai Hosp, Changhai Clin Res Unit, Shanghai, Peoples R China
来源
THERANOSTICS | 2024年 / 14卷 / 02期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
outer membrane vesicles; gastrointestinal tumors; genetic engineering; cargo delivery; tumor vaccine; GRAM-NEGATIVE BACTERIA; ESCHERICHIA-COLI; SALMONELLA-TYPHIMURIUM; DRUG-DELIVERY; CANCER; NANOPARTICLES; CELL; GOLD; LIPOPOLYSACCHARIDE; PEPTIDOGLYCAN;
D O I
10.7150/thno.85917
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Outer membrane vesicles (OMVs) are nanoscale lipid bilayer structures released by gram-negative bacteria. They share membrane composition and properties with their originating cells, making them adept at traversing cellular barriers. These OMVs have demonstrated exceptional membrane stability, immunogenicity, safety, penetration, and tumor-targeting properties, which have been leveraged in developing vaccines and drug delivery systems. Recent research efforts have focused on engineering OMVs to increase production yield, reduce cytotoxicity, and improve the safety and efficacy of treatment. Notably, gastrointestinal (GI) tumors have proven resistant to several traditional oncological treatment strategies, including chemotherapy, radiotherapy, and targeted therapy. Although immune checkpoint inhibitors have demonstrated efficacy in some patients, their usage as monotherapy remains limited by tumor heterogeneity and individual variability. The immunogenic and modifiable nature of OMVs makes them an ideal design platform for the individualized treatment of GI tumors. OMV-based therapy enables combination therapy and optimization of anti-tumor effects. This review comprehensively summarizes recent advances in OMV engineering for GI tumor therapy and discusses the challenges in the clinical translation of emerging OMV-based anti-tumor therapies.
引用
收藏
页码:761 / 787
页数:27
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