Lee Jeongjin, Um Wooram, Moon Hyungwon, Joo Hyeyeon, Song Yeari, Park Minsung, Yoon Been, Kim Hyun-Ryoung, Park Jae Hyung
Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University, 81 Irwon-ro, Seoul 06351, Republic of Korea.
Department of Biotechnology, Pukyong National University, 45 Yongso-ro, Busan 48513, Republic of Korea.
Pharmaceutics. 2022 Nov 25;14(12):2603. doi: 10.3390/pharmaceutics14122603.
Doxorubicin (DOX) is a representative anticancer drug with a unique ability to induce immunogenic cell death of cancer cells. However, undesired toxicity on immune cells has remained a significant challenge, hindering the usage of DOX in cancer immunotherapy. Here, we report a combined therapy to avoid the off-target toxicity of DOX by adapting ultrasound-responsive liposomal doxorubicin and focused ultrasound exposure. Histological analysis demonstrated that the combined therapy induced less hemosiderosis of splenocytes and improved tumor infiltration of cytotoxic T lymphocytes. Additionally, in vivo therapeutic evaluation results indicate that the combined therapy achieved higher efficacy when combined with PD-1 immune-checkpoint blockade therapy by improving immunogenicity.
阿霉素(DOX)是一种具有代表性的抗癌药物,具有诱导癌细胞发生免疫原性细胞死亡的独特能力。然而,其对免疫细胞产生的不良毒性仍是一个重大挑战,阻碍了DOX在癌症免疫治疗中的应用。在此,我们报告一种联合治疗方法,通过采用超声响应脂质体阿霉素和聚焦超声照射来避免DOX的脱靶毒性。组织学分析表明,联合治疗诱导的脾细胞含铁血黄素沉着较少,并改善了细胞毒性T淋巴细胞的肿瘤浸润。此外,体内治疗评估结果表明,联合治疗通过提高免疫原性,与PD-1免疫检查点阻断疗法联合使用时疗效更高。