Chen Yu, Guo Yu, Cheng Wen, Fan Jiahao, Li Jiacheng, Song Jiajia, Yang Xiaohai, Wang Kemin, Huang Jin
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha, 410082, P. R. China.
Adv Sci (Weinh). 2025 Jan;12(3):e2410632. doi: 10.1002/advs.202410632. Epub 2024 Nov 26.
Due to the inherent immunosuppression and immune evasion of cancer cells, combining photoimmunotherapy with immune checkpoint blockade leverages phototherapy and immune enhancement, overcoming mutual limitations and demonstrating significant anticancer potential. The main challenges include nonspecific accumulation of agents, uncontrolled activation, and drug carrier safety. Smart DNA nanospheres (NS) is developed with targeted delivery and controllable release of photosensitizers and immune agents to achieve effective synergistic therapy and minimize side effects. The multifunctional NS incorporate a targeting module for programming aptamers, a response module for programming i-motif and DNA/RNA hybrid sequences, and a therapeutic module for packaging photosensitizers and PD-L1 siRNA. NS navigate to the tumor site and are sequentially activated by intracellular acid and enzymes to release photosensitizers and programmed death ligand 1 (PD-L1) small interfering RNA (siRNA)a. Besides tumor killing and immune promotion, activated NS downregulate PD-L1 expression, alleviating immune tolerance and evasion, thus enhancing the immune response. These results indicate that NS significantly enhance antitumor immune responses, synergistically improve antitumor efficacy, and reduce systemic toxicity. This study broadens the application of DNA nanomaterials in precision drug delivery and tumor therapy.
由于癌细胞固有的免疫抑制和免疫逃逸特性,将光免疫疗法与免疫检查点阻断相结合,可利用光疗和免疫增强作用,克服相互的局限性,并展现出显著的抗癌潜力。主要挑战包括药物的非特异性积累、不受控制的激活以及药物载体的安全性。智能DNA纳米球(NS)通过对光敏剂和免疫剂进行靶向递送和可控释放而开发,以实现有效的协同治疗并将副作用降至最低。多功能NS包含用于编程适配体的靶向模块、用于编程i-基序和DNA/RNA杂交序列的响应模块,以及用于封装光敏剂和PD-L1小干扰RNA(siRNA)的治疗模块。NS可导航至肿瘤部位,并被细胞内的酸和酶依次激活,以释放光敏剂和程序性死亡配体1(PD-L1)小干扰RNA(siRNA)。除了杀伤肿瘤和促进免疫外,激活的NS还能下调PD-L1表达,减轻免疫耐受和逃逸,从而增强免疫反应。这些结果表明,NS能显著增强抗肿瘤免疫反应,协同提高抗肿瘤疗效,并降低全身毒性。本研究拓宽了DNA纳米材料在精准药物递送和肿瘤治疗中的应用。