Li Yuanxin, Li Bo, Wang Gang, Su Juanjuan, Qiao Yilin, Ma Chao, Wang Fan, Zhu Jian, Li Jingjing, Zhang Hongjie, Liu Kai, Xu Huji
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022 China.
University of Science and Technology of China, Hefei, 230026 China.
Nano Res. 2023 Jun 10:1-9. doi: 10.1007/s12274-023-5838-0.
Rheumatoid arthritis (RA) is a relatively common inflammatory disease that affects the synovial tissue, eventually results in joints destruction and even long-term disability. Although Janus kinase inhibitors (Jakinibs) show a rapid efficacy and are becoming the most successful agents in RA therapy, high dosing at frequent interval and severe toxicities cannot be avoided. Here, we developed a new type of fully compatible nanocarriers based on recombinant chimeric proteins with outstanding controlled release of upadacitinib. In addition, the fluorescent protein component of the nanocarriers enabled noninvasive fluorescence imaging of RA lesions, thus allowing real-time detection of RA therapy. Using rat models, the nanotherapeutic is shown to be superior to free upadacitinib, as indicated by extended circulation time and sustained bioefficacy. Strikingly, this nanosystem possesses an ultralong half-life of 45 h and a bioavailability of 4-times higher than pristine upadacitinib, thus extending the dosing interval from one day to 2 weeks. Side effects such as over-immunosuppression and leukocyte levels reduction were significantly mitigated. This smart strategy boosts efficacy, safety and visuality of Jakinibs in RA therapy, and potently enables customized designs of nanoplatforms for other therapeutics.
Supplementary material (further details of DLS analysis, biocompatibility of PCP-UPA, CIA models construction, etc.) is available in the online version of this article at 10.1007/s12274-023-5838-0.
类风湿性关节炎(RA)是一种相对常见的炎症性疾病,会影响滑膜组织,最终导致关节破坏甚至长期残疾。尽管Janus激酶抑制剂(Jakinibs)显示出快速疗效,并正在成为RA治疗中最成功的药物,但仍无法避免频繁高剂量给药和严重毒性。在此,我们基于重组嵌合蛋白开发了一种新型的完全兼容纳米载体,可实现乌帕替尼的出色控释。此外,纳米载体的荧光蛋白成分能够对RA病变进行无创荧光成像,从而实现对RA治疗的实时检测。使用大鼠模型,纳米疗法显示出优于游离乌帕替尼,表现为循环时间延长和生物疗效持续。引人注目的是,该纳米系统具有45小时的超长半衰期,生物利用度比原始乌帕替尼高4倍,从而将给药间隔从一天延长至两周。过度免疫抑制和白细胞水平降低等副作用得到显著缓解。这种智能策略提高了Jakinibs在RA治疗中的疗效、安全性和可视性,并有力地实现了针对其他疗法的纳米平台定制设计。
补充材料(DLS分析的进一步细节、PCP-UPA的生物相容性、CIA模型构建等)可在本文的在线版本中获取,链接为10.1007/s12274-023-5838-0。