A Self‐Delivery Nanodrug Simultaneously Inhibits COX‐2/PGE<sub>2</sub> Mediated Inflammation and Downregulates PD‐L1 to Boost Photoimmunotherapy
Jinmei Lai, Peiling Chen, Qun‐Ying Shi, Yongqi Xie, Gulijiayina Jiaerheng, Li‐Han Liu
Abstract
Abstract Phototherapy promotes anti‐tumor immunity by inducing immunogenic cell death (ICD), However, the accompanying inflammatory responses also trigger immunosuppression, attenuating the efficacy of photo‐immunotherapy. Herein, they co‐assembled a cell‐membrane targeting chimeric peptide C16‐Cypate‐RRKK‐PEG 8 ‐COOH (CCP) and anti‐inflammatory diclofenac (DA) to develop a nanodrug (CCP@DA) that both enhances the immune effect of phototherapy and weakens the inflammation‐mediated immunosuppression. CCP@DA achieves cell membrane‐targeting photodynamic and photothermal synergistic therapies to damage programmed death ligand 1 (PD‐L1) and induce a strong ICD to activate anti‐tumor response. Simultaneously, the released DA inhibits the cycoperoxidase‐2 (COX‐2)/prostaglandin E2 (PGE 2 ) pathway in tumor cells to inhibit pro‐tumor inflammation and further down‐regulate PD‐L1 expression to relieve the immunosuppressive microenvironment. CCP@DA significantly inhibited tumor growth and inflammation both in vitro and in vivo, while maintaining a potent anti‐tumor immune response. Additionally, it exhibits excellent anti‐metastatic capabilities and prolongs mouse survival time with a single dose and low levels of near‐infrared (NIR) light exposure. This work provides a valuable strategy to control the therapy‐induced inflammation for high‐efficiency photoimmunotherapy.