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pH敏感型磷酸化壳聚糖水凝胶作为用于肌肉注射免疫的疫苗递送系统。

pH Sensitive phosphorylated chitosan hydrogel as vaccine delivery system for intramuscular immunization.

作者信息

Wei Jianye, Xue Wei, Yu Xifei, Qiu Xiaozhong, Liu Zonghua

机构信息

1 Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, Jinan University, Guangzhou, China.

2 The Polymer Composites Engineering Laboratory, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, China.

出版信息

J Biomater Appl. 2017 May;31(10):1358-1369. doi: 10.1177/0885328217704139. Epub 2017 Apr 7.

DOI:10.1177/0885328217704139
PMID:28387574
Abstract

In the field of immunotherapy, immune vaccinations have received more and more attention for disease prevention and treatment. In immune vaccination, efficient vaccine adjuvants are necessary due to the weak immunogenicity of vaccines. Some traditional vaccine adjuvants have been widely used but have shown obvious limitations such as poor biosafety. Therefore, researchers make a great effort to develop more functional novel immune adjuvants such as chitosan-based immune adjuvants. However, chitosan is poorly water soluble, which greatly limits its application as immune adjuvants, regardless of its good biocompatibility, biodegradability, and other biological activities. In this work, we prepared a water-soluble chitosan derivative phosphorylated chitosan (PCS) and evaluated its potential as a novel immune adjuvant. PCS was found to be pH sensitive: specifically, it was water soluble at pH < 7.0 but began to gel at pH >7.0. By virtue of this, neutral PCS aqueous solutions containing ovalbumin (OVA) antigen was intramuscularly injected into test mice, which would transform to an OVA-containing gel network for OVA immunization. The results showed that the use of 30 mg/mL PCS-based hydrogel as vaccine delivery system contributed to significantly higher level of antigen-specific immune responses, including higher level of antigen-specific IgG antibodies, IFN-γ and IL-4 cytokines secretion by splenocytes, as well as memory CD4 and CD8 T cells. In vivo imaging and immunohistochemistry assays suggest that the improved immunization efficacy may be attributed to the controlled release of antigen from injection site by PCS gel network, and then prolonged antigen stimuli to the immune system. From the results, PCS could be developed as a promising vaccine delivery system for immunotherapy.

摘要

在免疫治疗领域,免疫疫苗在疾病预防和治疗方面受到了越来越多的关注。在免疫接种中,由于疫苗的免疫原性较弱,高效的疫苗佐剂是必不可少的。一些传统的疫苗佐剂已被广泛使用,但已显示出明显的局限性,如生物安全性差。因此,研究人员致力于开发更多功能性的新型免疫佐剂,如基于壳聚糖的免疫佐剂。然而,壳聚糖的水溶性较差,这极大地限制了其作为免疫佐剂的应用,尽管它具有良好的生物相容性、生物降解性和其他生物活性。在这项工作中,我们制备了一种水溶性壳聚糖衍生物磷酸化壳聚糖(PCS),并评估了其作为新型免疫佐剂的潜力。发现PCS对pH敏感:具体而言,它在pH < 7.0时可溶于水,但在pH > 7.0时开始凝胶化。据此,将含有卵清蛋白(OVA)抗原的中性PCS水溶液肌肉注射到试验小鼠体内,其会转变为用于OVA免疫的含OVA凝胶网络。结果表明,使用30 mg/mL基于PCS的水凝胶作为疫苗递送系统有助于显著提高抗原特异性免疫反应水平,包括更高水平的抗原特异性IgG抗体、脾细胞分泌的IFN-γ和IL-4细胞因子,以及记忆性CD4和CD8 T细胞。体内成像和免疫组织化学分析表明,免疫效果的提高可能归因于PCS凝胶网络对注射部位抗原的控释,进而延长了抗原对免疫系统的刺激。从结果来看,PCS有望被开发成为一种用于免疫治疗的疫苗递送系统。

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