Wang Xiaoting, Dai Yang, Zhao Song, Tang Jianxia, Li Hongjun, Xing Yuntian, Qu Guoli, Li Xinsong, Dai Jianrong, Zhu Yinchang, Zhang Xueguang
Jiangsu Stem Cell Key Laboratory, Institute of Medical Biotechnology, Medical College of Soochow University; Jiangsu Institute of Clinical Immunology, The First Affiliated Hospital of Soochow University, Suzhou, China ; Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, Wuxi, Jiangsu, China.
Jiangsu Institute of Parasitic Diseases, Key Laboratory on Technology for Parasitic Disease Prevention and Control, Ministry of Health, Jiangsu Provincial Key Laboratory on Molecular Biology of Parasites, Wuxi, Jiangsu, China.
PLoS One. 2014 Jan 30;9(1):e86578. doi: 10.1371/journal.pone.0086578. eCollection 2014.
Schistosomiasis japonica remains a major public-health concern in China. Praziquantel-based chemotherapy effectively reduces both infections and intensity; however, it can not prevent re-infection. Furthermore, there is an increasing concern about praziquantel resistance following long-term repeated use of the drug in endemic areas. Therefore, development of a schistosomiasis vaccine, as a strategy to prevent and control schistosomiasis japonica, has been given high priority. The present study was conducted to develop PAMAM dendrimers as a novel vaccine delivery vector for a schistosomiasis japonica DNA vaccine and evaluate its ability to enhance protective effects against Schistosoma japonicum infection.
METHODOLOGY/PRINCIPAL FINDINGS: Lysine was used to modify 4.0G PAMAM, and the modified product PAMAM-Lys was synthesized. PAMAM-Lys showed both high transfection and low cytotocity for gene delivery in vitro. DNA vaccines combined with PAMAM-Lys produced higher level of protection compare with naked DNA vaccines against S. japonicum infection in a mouse model. Futhermore,antibodies from mice immunized with PAMAM-Lys combined DNA vaccines were significantly higher than those of mice immunized with the naked DNA vaccines. The PAMAM-Lys vector elicited a predominantly IgG2a antibody response and a tremendously increase in the production of IL-2 and IFN-γ.
CONCLUSION/SIGNIFICANCE: Lysine-modified PAMAM-Lys is an excellent vector. PAMAM-Lys may enhance the immunoreactivity of DNA vaccine and increase the protective effect of the SjC23 DNA vaccine against S. japonicum infection.
日本血吸虫病仍是中国主要的公共卫生问题。基于吡喹酮的化疗能有效降低感染率和感染强度;然而,它无法预防再感染。此外,在流行地区长期重复使用该药物后,对吡喹酮耐药性的担忧日益增加。因此,开发血吸虫病疫苗作为预防和控制日本血吸虫病的策略已被高度重视。本研究旨在开发聚酰胺 - 胺(PAMAM)树枝状大分子作为日本血吸虫病DNA疫苗的新型疫苗递送载体,并评估其增强针对日本血吸虫感染的保护作用的能力。
方法/主要发现:用赖氨酸修饰4.0G PAMAM,合成修饰产物PAMAM-Lys。PAMAM-Lys在体外基因递送中表现出高转染率和低细胞毒性。与裸DNA疫苗相比,与PAMAM-Lys联合的DNA疫苗在小鼠模型中对日本血吸虫感染产生了更高水平的保护作用。此外,用PAMAM-Lys联合DNA疫苗免疫的小鼠产生的抗体明显高于用裸DNA疫苗免疫的小鼠。PAMAM-Lys载体引发了主要为IgG2a抗体反应,并极大地增加了IL-2和IFN-γ的产生。
结论/意义:赖氨酸修饰的PAMAM-Lys是一种优良的载体。PAMAM-Lys可能增强DNA疫苗的免疫反应性,并提高SjC23 DNA疫苗对日本血吸虫感染的保护作用。