Hybridoma-inspired strategy crafts tailored multifunctional exosomes for precision therapy

• 成果类型: Article
• 署名作者: Dong, Zhufeng; Yin, Tieyin; Deng, Zhiqin; Zou, Hang; Kuang, Lei; Wang, Yang; Shi, Wen; Han, Mengwei; Zhu, Siqing; Wang, Zheng; Hu, Xiaoye; Wang, Yazhou Z.
• 署名单位: Chongqing University; Chongqing University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-14729
• DOI: 10.1073/pnas.2424547122
• 发表日期: 2025-09-16
• 关键词: amyloid-beta; alzheimers; neutrophils; microglia; pathology; DYNAMICS

摘要

Engineering functional exosomes represents a cutting-edge approach in biomedicine, holding the promise to transform targeted therapy. However, challenges such as achieving consistent modification and scalability have limited their wider adoption. Herein, we introduce a universal and effective strategy for engineering multifunctional exosomes through cell fusion. The hybrid-cell-derived exosomes could combine the functional properties of both parental cells and be readily produced by passaging. This method enables customization and large-scale production of exosomes with specific functionalities, potentially advancing precision therapies across a wide array of diseases. As demonstrated in Alzheimer's disease (AD) models, exosomes derived from hybrid cells (HCs) (H/Exos) of mesenchymal stem cells (MSCs) and neutrophils efficiently targeted AD-affected areas via LFA-1/ICAM-1 and improved the cognition of AD mice. Beyond directly promoting neural repair and inhibiting inflammation, we surprisingly found that H/Exos increased microglia abundance, modulated microglia gene expression, enhanced the endocytic and lysosomal function, and promoted microglial phagocytic phenotypic differentiation to clear A beta. This hybridoma-inspired strategy offers a versatile and practical way to engineer exosomes with desired therapeutic functions, representing a promising direction for personalized therapies.