Key Laboratory of Natural Medicine and Immune Engineering, Henan University, Kaifeng, Henan, 475004, China.
State Key Laboratory of Antiviral Drugs, Henan University, China.
Small. 2024 Jul;20(30):e2310565. doi: 10.1002/smll.202310565. Epub 2024 Feb 23.
Immunotherapy utilizing anti-PD-L1 blockade has achieved dramatic success in clinical breast cancer management but is often hampered by the limited immune response. Increasing evidence shows that immunogenic cell death (ICD) recently arises as a promising strategy for enlarging tumor immunogenicity and eliciting systemic anti-tumor immunity effectively. However, developing simple but versatile, highly efficient but low-toxic, biosafe, and clinically available transformed ICD inducers remains a huge demand and is highly desirable. Herein, a multifunctional ICD inducer is purposefully developed A6-MPDA@PAL by integrating photothermal therapy (PTT) nanoplatforms mesoporous polydopamine (MPDA), CDK4/6 inhibitor palbociclib (PAL), and CD44-specific targeting A6 peptide in a simple way for augmenting the immune antitumor efficacy of anti-PD-L1 therapy. Remarkably, the light-inducible nanoplatforms exhibit multiple favorable therapeutic features ensuring a superior and biosafe PTT/chemotherapy efficacy. Together with stronger accumulative ICD induction, single administration of A6-MPDA@PAL can trigger robust systemic antitumor immunity and abscopal effect with the assistance of anti-PD-L1 blockade by fascinating the intratumoral infiltration of T lymphocytes and reversing the immunosuppressive tumor microenvironment simultaneously, therapy achieving brilliant synergistic immunotherapy with effective tumor ablation. This study presents a simple and smart ICD inducer opening up attractive clinical possibilities for reinforcing the anti-PD-L1 therapy against breast cancer.
免疫疗法利用抗 PD-L1 阻断已在乳腺癌临床管理中取得了显著成功,但往往受到有限免疫反应的阻碍。越来越多的证据表明,免疫原性细胞死亡(ICD)最近成为一种有前途的策略,可以扩大肿瘤免疫原性并有效引发全身抗肿瘤免疫。然而,开发简单但多功能、高效但低毒、生物安全且临床可用的转化 ICD 诱导剂仍然是一个巨大的需求,这是非常理想的。在此,通过将光热治疗(PTT)纳米平台介孔聚多巴胺(MPDA)、CDK4/6 抑制剂帕博西尼(PAL)和 CD44 特异性靶向 A6 肽整合到一个简单的多功能 ICD 诱导剂 A6-MPDA@PAL 中,以增强抗 PD-L1 治疗的免疫抗肿瘤疗效。值得注意的是,光诱导纳米平台具有多种有利的治疗特性,确保了卓越的生物安全 PTT/化疗效果。与更强的累积 ICD 诱导相结合,单次给予 A6-MPDA@PAL 可以在抗 PD-L1 阻断的辅助下触发强大的全身抗肿瘤免疫和远隔效应,通过吸引 T 淋巴细胞在肿瘤内浸润并同时逆转免疫抑制性肿瘤微环境,实现有效的肿瘤消融协同免疫治疗。本研究提出了一种简单而智能的 ICD 诱导剂,为增强抗 PD-L1 疗法治疗乳腺癌提供了有吸引力的临床可能性。