National Glycoengineering Research Center, Shandong Key Laboratory of Carbohydrate Chemistry and Glycobiology, NMPA Key Laboratory for Quality Research and Evaluation of Carbohydrate-based Medicine, Shandong University, Qingdao, Shandong, 266237, China.
National Glycoengineering Research Center, Shandong Key Laboratory of Carbohydrate Chemistry and Glycobiology, NMPA Key Laboratory for Quality Research and Evaluation of Carbohydrate-based Medicine, Shandong University, Qingdao, Shandong, 266237, China; State Key Laboratory of Microbial Technology, Shandong University, Qingdao, Shandong, 266237, China.
Biomaterials. 2021 Jun;273:120792. doi: 10.1016/j.biomaterials.2021.120792. Epub 2021 Apr 8.
The race is on for therapeutic agents that stop cancer. An effective vaccine offers a safe and promising approach for cancer immunotherapy. However, substantial barriers to immunotherapy in cancer vaccines include the low immunogenicity of cancer antigens and the immunosuppression commonly present in solid tumors, resulting in significant challenges for developing a clinically effective cancer vaccine. Here, the state of the art of synergistic therapy, which includes the photothermal effect combined with immunotherapy, was investigated to target tumors. For the first time, indocyanine green (ICG, referred to as I), imiquimod (R837, referred to as R) and a foreign cytotoxic T lymphocyte antigen peptide (CTL-Ap, referred to as Ap) with the sequence of SIINFEKL from ovalbumin (OVA) were encapsulated by acetalated dextran (AcDEX) to form nanoparticles (NPs) averaging 92 nm in diameter as an immunogen. Administration of the resulting multifunctional vaccine I-R-Ap-AcDEX NPs enhanced antitumor cytotoxic T lymphocyte (CTL) immunotherapy. On the one hand, subcutaneous immunization of the NPs allows foreign Ap to enter the major histocompatibility complex class I (MHC-I) cross-presentation pathway of antigen-presenting cells, thereby presenting Ap and eliciting high levels of Ap-specific CTLs. On the other hand, intratumor/intravenous injections of the NPs allow foreign Ap to enter tumor cells and present Ap through the MHC-I cross-presentation pathway. Ap-specific CTLs can kill Ap-presented tumor cells. Furthermore, the NPs generated near-infrared laser triggered the photothermal killing of tumor cells. To our knowledge, this is the first report of AcDEX NPs in antitumor photothermal therapy. Strikingly, systemic administration of the I-R-Ap-AcDEX NPs combined with near-infrared laser irradiation allowed for complete protection to mice from the tumors when applied to two non-OVA tumor models. This quite impressive result displays the great promise of synergistic therapy by the vaccine I-R-Ap-AcDEX NPs, an approach that harnesses the photothermal effect to boost antitumor immunotherapy.
癌症治疗药物的研发竞赛正在进行中。有效的疫苗为癌症免疫疗法提供了一种安全且有前景的方法。然而,癌症疫苗免疫疗法存在实质性障碍,包括癌症抗原的免疫原性低和实体瘤中常见的免疫抑制,这给开发临床有效的癌症疫苗带来了重大挑战。在这里,研究了协同治疗的最新进展,包括光热效应与免疫疗法相结合,以靶向肿瘤。首次将吲哚菁绿(ICG,简称 I)、咪喹莫特(R837,简称 R)和来自卵清蛋白(OVA)的序列为 SIINFEKL 的外源性细胞毒性 T 淋巴细胞抗原肽(CTL-Ap,简称 Ap)用缩醛化葡聚糖(AcDEX)包裹,形成平均直径为 92nm 的纳米颗粒(NPs)作为免疫原。施用所得多功能疫苗 I-R-Ap-AcDEX NPs 增强了抗肿瘤细胞毒性 T 淋巴细胞(CTL)免疫疗法。一方面,NPs 的皮下免疫使外源性 Ap 进入抗原呈递细胞的主要组织相容性复合体 I (MHC-I)交叉呈递途径,从而呈递 Ap 并引发高水平的 Ap 特异性 CTL。另一方面,NPs 的肿瘤内/静脉内注射使外源性 Ap 进入肿瘤细胞,并通过 MHC-I 交叉呈递途径呈递 Ap。Ap 特异性 CTL 可以杀死呈递 Ap 的肿瘤细胞。此外,NPs 产生的近红外激光触发了肿瘤细胞的光热杀伤。据我们所知,这是 AcDEX NPs 在抗肿瘤光热治疗中的首次报道。引人注目的是,当应用于两种非 OVA 肿瘤模型时,系统给予 I-R-Ap-AcDEX NPs 联合近红外激光照射可使小鼠完全免受肿瘤的影响。这一令人印象深刻的结果显示了疫苗 I-R-Ap-AcDEX NPs 协同治疗的巨大潜力,该方法利用光热效应来增强抗肿瘤免疫疗法。