State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Biomaterials. 2021 Feb;269:120609. doi: 10.1016/j.biomaterials.2020.120609. Epub 2020 Dec 18.
The robust immunosuppressive microenvironment in tumor represents a key challenge of cancer treatment, and their modulations by versatile therapeutic agents are critically hampered by the limited intratumoral delivery. Herein, we report a bioinspired tumor-responsive theranostic nanovehicle (BTN) with striking tumor-penetrating capability to relieve the profound immunosuppression in tumor for effective cancer therapy. BTN is designed by loading tumor-activated melittin pro-peptide, theranostic photochlor and reactive oxygen species (ROS)-responsive prodrug of chemo-immunomodulator gemcitabine into a bioinspired lipoprotein-based nanovehicle, which display prominent tumor accumulation and flexible intratumoral permeation. Notably, the BTN-mediated combinational treatment caused drastic elimination of multiple immunosuppressive cells and remarkable infiltration of cytotoxic lymphocytes in tumor, thereby essentially relieving the tumor immunosuppression and strikingly depressing the tumor growth. Therefore, this design provides an encouraging delivery nanoplatform with distinguished immunosuppression-relieving capacity for effective cancer therapy.
肿瘤内强大的免疫抑制微环境是癌症治疗的一个关键挑战,而通过各种治疗剂对其进行调节受到了肿瘤内递药有限性的严重阻碍。在此,我们报告了一种具有惊人肿瘤穿透能力的仿生肿瘤响应治疗性纳米载体(BTN),可缓解肿瘤中深刻的免疫抑制,从而实现有效的癌症治疗。BTN 的设计是通过将肿瘤激活的蜂毒素原肽、治疗性光氯和化疗免疫调节剂吉西他滨的 ROS 响应前药装载到仿生脂蛋白纳米载体中实现的,该载体显示出明显的肿瘤积累和灵活的肿瘤内渗透。值得注意的是,BTN 介导的联合治疗导致多种免疫抑制细胞的急剧消除和肿瘤内细胞毒性淋巴细胞的显著浸润,从而从根本上缓解了肿瘤的免疫抑制,并显著抑制了肿瘤生长。因此,该设计为有效的癌症治疗提供了一种具有出色免疫抑制缓解能力的有希望的递药纳米平台。