Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.
University of Science and Technology of China, Hefei, 230026, P. R. China.
Macromol Biosci. 2021 Jun;21(6):e2100049. doi: 10.1002/mabi.202100049. Epub 2021 Apr 19.
Combination therapy can be used to enhance the therapeutic response and decrease side effects during cancer treatment. In this study, a system is developed to locally deliver the immune checkpoint blockade antibody targeting programmed death-ligand 1 (anti-PD-L1 or aPD-L1) and doxorubicin (Dox), by an injectable, biocompatible polypeptide hydrogel as a drug depot. The localized and sustained release of Dox after the intratumoral injection of the co-loaded hydrogel induces immunogenic tumor cell death, thus promoting an antitumor immunological response. The tumor inhibitory effect is significantly enhanced by the simultaneous release of aPD-L1 at the tumor site thanks to its action on the inhibition of the PD-1/PD-L1 pathway and restoration of the tumor-killing effect of cytotoxic T cells. Treatment of the B16F10 melanoma model with the aPD-L1 and Dox co-loaded hydrogel leads to a remarkable inhibition of tumor progression and prolongation of animal survival.
联合治疗可用于增强癌症治疗过程中的治疗反应并降低副作用。在这项研究中,开发了一种系统,通过可注射的、生物相容性的多肽水凝胶作为药物库来局部递送针对程序性死亡配体 1(抗 PD-L1 或 aPD-L1)和多柔比星(Dox)的免疫检查点阻断抗体。肿瘤内注射共载药水凝胶后,Dox 的局部和持续释放诱导免疫原性肿瘤细胞死亡,从而促进抗肿瘤免疫反应。由于 aPD-L1 在肿瘤部位的作用是抑制 PD-1/PD-L1 通路并恢复细胞毒性 T 细胞的杀伤作用,因此同时释放 aPD-L1 可显著增强肿瘤抑制作用。用载有 aPD-L1 和 Dox 的水凝胶治疗 B16F10 黑色素瘤模型可显著抑制肿瘤进展并延长动物存活时间。
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