Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Institute of Functional Nano and Soft Materials (FUNSOM), Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou, Jiangsu 215123, China.
School of Life Sciences, Shanghai University, Shanghai 200444, China.
Nano Lett. 2022 Jun 8;22(11):4509-4518. doi: 10.1021/acs.nanolett.2c01332. Epub 2022 May 20.
Despite the tremendous progresses of cancer immunotherapy, its current clinical responses rate in melanoma remains to be improved. Here, we have reported a skin penetrating tetrahedral framework nucleic acid immune adjuvant (FNAIA) to transdermally deliver chemotherapy drugs into melanoma to induce the immunogenic death of tumor cells and expose tumor antigens, which with assistance of CpG oligodeoxynucleotide incorporated in FNAIA could trigger systemic tumor-specific immune responses. Compared with free CpG, FNAIA could penetrate deeper into subcutaneous tumor tissues and more effectively stimulate dendritic cell maturation. Notably, doxorubicin-loaded FNAIA locally applied on the intact skin above the melanoma could effectively inhibit the growth of mouse B16F10 melanoma and increase tumor CD8 T cell infiltration. Moreover, combined with immune checkpoint inhibitor, the growth of distant tumors could also be effectively inhibited, suggesting that this strategy could induce systemic immune responses. Therefore, this work provides a new idea for non-invasive treatment of skin cancer.
尽管癌症免疫疗法取得了巨大进展,但目前其在黑色素瘤中的临床应答率仍有待提高。在这里,我们报告了一种透皮四面体框架核酸免疫佐剂(FNAIA),可将化疗药物经皮递送至黑色素瘤中,以诱导肿瘤细胞的免疫原性死亡并暴露肿瘤抗原,这在 FNAIA 中掺入的 CpG 寡脱氧核苷酸的辅助下,可以引发全身性的肿瘤特异性免疫反应。与游离 CpG 相比,FNAIA 可以更深地渗透到皮下肿瘤组织中,并更有效地刺激树突状细胞成熟。值得注意的是,阿霉素负载的 FNAIA 局部应用于黑色素瘤上方完整的皮肤上,可有效抑制小鼠 B16F10 黑色素瘤的生长,并增加肿瘤 CD8 T 细胞浸润。此外,与免疫检查点抑制剂联合使用,还可以有效抑制远处肿瘤的生长,表明该策略可以诱导全身性免疫反应。因此,这项工作为非侵入性治疗皮肤癌提供了新的思路。
ACS Appl Mater Interfaces. 2022-8-31
J Invest Dermatol. 2008-9
Front Immunol. 2025-8-8