Department of Orthopaedic Surgery, Zhongshan Hospital, Fudan University, Shanghai, 200032, P. R. China.
Cancer center, Zhongshan Hospital, Fudan University, Shanghai, 200032, P. R. China.
Adv Healthc Mater. 2022 Oct;11(20):e2200938. doi: 10.1002/adhm.202200938. Epub 2022 Aug 11.
Although immune checkpoint inhibitors (ICIs) have been widely applied to treat non-small cell lung cancer (NSCLC), a significant proportion of patients, especially those with spinal metastasis (NSCLC-SM), are insensitive to anti-programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) ICIs. A drug delivery nano-controller of PD-L1 that targets NSCLC-SM can solve this problem, however, none have been developed to date. In this study, it is shown that integrin β3 (β3-int) is strongly upregulated in NSCLC-SM. Its inhibitor RGDyK promotes PD-L1 ubiquitination, indicating the potential application of RGDyK as a new PD-L1 inhibitor in nano-controller and a targeting peptide for NSCLC-SM treatment. According to the synergistic effect of photodynamic therapy and ICIs on T-cell activation through the release of tumor antigens, RGDyK-modified and zinc protoporphyrin (ZnPP)-loaded mesoporous silicon nanoparticles (ZnPP@MSN-RGDyK) are fabricated. The ZnPP@MSN-RGDyK nanoparticles precisely target β3-int to inhibit PD-L1, exhibiting high photodynamic therapy efficiency, and excellent immunotherapeutic effects in an NSCLC-SM mouse model. Collectively, the findings indicate that ZnPP@MSN-RGDyK is a promising immunotherapeutic agent for treating NSCLC-SM.
尽管免疫检查点抑制剂(ICIs)已被广泛应用于治疗非小细胞肺癌(NSCLC),但仍有相当一部分患者,尤其是那些伴有脊柱转移(NSCLC-SM)的患者,对抗程序性死亡 1(PD-1)/程序性死亡配体 1(PD-L1)ICI 不敏感。针对 NSCLC-SM 的 PD-L1 药物输送纳米控制器可以解决这个问题,但目前还没有开发出来。在这项研究中,研究表明整合素 β3(β3-int)在 NSCLC-SM 中强烈上调。其抑制剂 RGDyK 促进 PD-L1 的泛素化,表明 RGDyK 作为纳米控制器中的新型 PD-L1 抑制剂和 NSCLC-SM 治疗的靶向肽具有潜在应用价值。根据光动力疗法和 ICI 通过释放肿瘤抗原对 T 细胞激活的协同作用,制备了 RGDyK 修饰和锌原卟啉(ZnPP)负载介孔硅纳米粒子(ZnPP@MSN-RGDyK)。ZnPP@MSN-RGDyK 纳米颗粒精确靶向β3-int 以抑制 PD-L1,在 NSCLC-SM 小鼠模型中表现出高的光动力治疗效率和优异的免疫治疗效果。总之,这些发现表明 ZnPP@MSN-RGDyK 是一种有前途的治疗 NSCLC-SM 的免疫治疗药物。