抗体
免疫系统
药物输送
抗原
全身给药
医学
细胞毒性T细胞
癌症研究
药理学
口服
不利影响
治疗指标
毒品携带者
免疫学
药品
化学
生物
材料科学
纳米技术
生物化学
体内
体外
生物技术
作者
Wenjun Zhu,Yu Chao,Qiutong Jin,Linfu Chen,Jingjing Shen,Jiafei Zhu,Yu Chai,Panhao Lu,Nailin Yang,Muchao Chen,Yang Yang,Qian Chen,Zhuang Liu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-02-19
卷期号:17 (5): 4373-4386
被引量:24
标识
DOI:10.1021/acsnano.2c09266
摘要
Therapeutic proteins are playing increasingly important roles in treating numerous types of diseases. However, oral administration of proteins, especially large ones (e.g., antibodies), remains a great challenge due to their difficulties in penetrating intestinal barriers. Herein, fluorocarbon-modified chitosan (FCS) is developed for efficient oral delivery of different therapeutic proteins, in particular large ones such as immune checkpoint blockade antibodies. In our design, therapeutic proteins are mixed with FCS to form nanoparticles, lyophilized with appropriate excipients, and then filled into enteric capsules for oral administration. It has been found that FCS could promote transmucosal delivery of its cargo protein via inducing transitory rearrangement of tight junction associated proteins between intestinal epithelial cells and subsequently release free proteins into blood circulation. It is shown that at a 5-fold dose oral delivery of anti-programmed cell death protein-1 (αPD1) or its combination with anti-cytotoxic T-lymphocyte antigen 4 (αCTLA4) using this method could achieve comparable antitumor therapeutic responses to that achieved by intravenous injection of corresponding free antibodies in various types of tumor models and, more excitingly, result in significantly reduced immune-related adverse events. Our work successfully demonstrates the enhanced oral delivery of antibody drugs to achieve systemic therapeutic responses and may revolutionize the future clinical usage of protein therapeutics.
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