Xu Yuchun, Yan Xiaoying, Zhang Fengrui, Li Qiaofeng, Wei Ting, Xiao Zhisheng, Chai Yu, Wang Chunjie, Liu Zhuang
Institute of Functional Nano & Soft Materials (FUNSOM), Collaborative Innovation Center of Suzhou Nano Science and Technology, Jiangsu Key Laboratory for Carbon-based Functional Materials and Devices, Soochow University, Suzhou 215123, China.
College of Nano Science and Technology, Soochow University, Suzhou 215213, China.
ACS Nano. 2025 Aug 26;19(33):30046-30059. doi: 10.1021/acsnano.5c05354. Epub 2025 Aug 12.
Persistent infection with high-risk human papillomavirus (HPV) is widely acknowledged as the leading cause of cervical, oral, and other malignant cancers. Currently approved HPV vaccines are prophylactic and show no significant therapeutic effect on pre-existing infections or lesions. Considering the important role of mucosal vaccines in inducing localized immune responses against mucosal cancer, in this work, we developed salcaprozate-modified chitosan (SCS) for intranasal delivery of the HPV vaccine. We found that SCS can self-assemble with the E7 (RAHYNIVTF) and the immune adjuvant CpG to form nanoparticles, enabling penetration through the nasal mucosal barrier. This nanovaccine not only showed potent antitumor efficacy in subcutaneous tumor models but also induced stronger antigen-specific mucosal immune responses and systemic cellular immunity in oropharyngeal cancers and cervical cancer models, compared to traditional intramuscular injection. Therefore, our work presents a noninvasive carrier for effective intranasal delivery of nanovaccines, showing advantages in triggering more potent mucosal immunity while presenting enhanced patient compliance.
高危型人乳头瘤病毒(HPV)的持续感染被广泛认为是宫颈癌、口腔癌和其他恶性肿瘤的主要病因。目前获批的HPV疫苗属于预防性疫苗,对已有的感染或病变并无显著治疗效果。鉴于黏膜疫苗在诱导针对黏膜癌的局部免疫反应中发挥的重要作用,在本研究中,我们开发了用于鼻腔递送HPV疫苗的水杨酸盐修饰壳聚糖(SCS)。我们发现,SCS能与E7(RAHYNIVTF)和免疫佐剂CpG自组装形成纳米颗粒,从而穿透鼻黏膜屏障。与传统肌肉注射相比,这种纳米疫苗不仅在皮下肿瘤模型中展现出强大的抗肿瘤功效,还在口咽癌和宫颈癌模型中诱导了更强的抗原特异性黏膜免疫反应和全身细胞免疫。因此,我们的研究提供了一种用于有效鼻腔递送纳米疫苗的非侵入性载体,在触发更强大的黏膜免疫方面具有优势,同时提高了患者的依从性。