Engineered exosome nanovesicles for delivery of antibodies to treat inflammatory bowel disease

Inflammatory bowel disease (IBD) is characterized by chronic inflammation and impaired immune tolerance, for which current therapies provide only partial and transient relief. Here, we introduce PrEXO-a23, a biomimetic nanotherapeutic engineered by fusing regulatory T cell (Treg)-derived exosomes with platelet membrane vesicles and conjugating interleukin-23 (IL-23) antibodies via a matrix metalloproteinase (MMP)-cleavable linker. This design exploits the inherent homing ability of platelets and Tregs, enabling PrEXO-a23 to preferentially accumulate in inflamed colonic tissues in murine IBD models. At the disease site, elevated MMP activity triggers antibody release to inhibit IL-23-mediated inflammation, while exosomal cargo reprograms dendritic cells and promotes Treg expansion, thereby restoring immune tolerance. This dual-action strategy significantly alleviates IBD, prevents complications like intestinal fibrosis and colitis-associated colorectal cancer, and shows p53-dependent efficacy in carcinogenesis prevention. These findings highlight PrEXO-a23 as a promising nanotherapeutic platform for durable immune reprogramming and long-term IBD management.

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Publication Details

Journal
Nature Communications
Published
2026-02-13
DOI
https://doi.org/10.1038/s41467-026-69382-4
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00

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article

Engineered exosome nanovesicles for delivery of antibodies to treat inflammatory bowel disease

Baisong Zhu, Lin Mei, Jiahui Cao, Jinxie Zhang et al.
Nature Communications
Extracellular vesicles in disease
article

Engineered exosome nanovesicles for delivery of antibodies to treat inflammatory bowel disease

Baisong Zhu, Lin Mei, Jiahui Cao, Jinxie Zhang, Yao-Xin Lin, Rourou Miao, Ran Luo, Yiqiu Fu, Meitong Ou, Zhuo Mao, Hanjie Zhang, Fan Zhang, Wenfeng Zeng, Liu Yu, Xinyi Wang, Wen Li
article en

Abstract

Inflammatory bowel disease (IBD) is characterized by chronic inflammation and impaired immune tolerance, for which current therapies provide only partial and transient relief. Here, we introduce PrEXO-a23, a biomimetic nanotherapeutic engineered by fusing regulatory T cell (Treg)-derived exosomes with platelet membrane vesicles and conjugating interleukin-23 (IL-23) antibodies via a matrix metalloproteinase (MMP)-cleavable linker. This design exploits the inherent homing ability of platelets and Tregs, enabling PrEXO-a23 to preferentially accumulate in inflamed colonic tissues in murine IBD models. At the disease site, elevated MMP activity triggers antibody release to inhibit IL-23-mediated inflammation, while exosomal cargo reprograms dendritic cells and promotes Treg expansion, thereby restoring immune tolerance. This dual-action strategy significantly alleviates IBD, prevents complications like intestinal fibrosis and colitis-associated colorectal cancer, and shows p53-dependent efficacy in carcinogenesis prevention. These findings highlight PrEXO-a23 as a promising nanotherapeutic platform for durable immune reprogramming and long-term IBD management.

Nature CommunicationsVol. 17(1)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), National Center for Nanoscience and Technology (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Chinese Academy of Medical Sciences, Natural Science Foundation of Tianjin City, Peking Union Medical College, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Science Fund for Distinguished Young Scholars of Tianjin, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 56%
Extracellular vesicles in disease
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