Yuan Zi-Guo, Zhang Xiu-Xiang, He Xian-Hui, Petersen Eskild, Zhou Dong-Hui, He Yong, Lin Rui-Qing, Li Xiu-Zhen, Chen Xu-Li, Shi Xiao-Ru, Zhong Xiu-Ling, Zhang Bing, Zhu Xing-Quan
Department of Parasitology, State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, CAAS, Lanzhou, Gansu Province 730046, PR China.
Clin Vaccine Immunol. 2011 Jan;18(1):119-24. doi: 10.1128/CVI.00312-10. Epub 2010 Nov 24.
Toxoplasma gondii can infect a large variety of domestic and wild animals and human beings, sometimes causing severe pathology. Rhoptries are involved in T. gondii invasion and host cell interaction and have been implicated as important virulence factors. In this study, we constructed a DNA vaccine expressing rhoptry protein 16 (ROP16) of T. gondii and evaluated the immune responses it induced in Kunming mice. The gene sequence encoding ROP16 was inserted into the eukaryotic expression vector pVAX I. We immunized Kunming mice intramuscularly. After immunization, we evaluated the immune response using a lymphoproliferative assay, cytokine and antibody measurements, and the survival times of mice challenged lethally. The results showed that mice immunized with pVAX-ROP16 developed a high level of specific antibody responses against T. gondii ROP16 expressed in Escherichia coli, a strong lymphoproliferative response, and significant levels of gamma interferon (IFN-γ), interleukin-2 (IL-2), IL-4, and IL-10 production compared with results for other mice immunized with either empty plasmid or phosphate-buffered saline, respectively. The results showed that pVAX-ROP16 induces significant humoral and cellular Th1 immune responses. After lethal challenge, the mice immunized with pVAX-ROP16 showed a significantly (P < 0.05) prolonged survival time (21.6 ± 9.9 days) compared with control mice, which died within 7 days of challenge. Our data demonstrate, for the first time, that ROP16 triggers a strong humoral and cellular response against T. gondii and that ROP16 is a promising vaccine candidate against toxoplasmosis, worth further development.
刚地弓形虫可感染多种家畜、野生动物及人类,有时会引发严重病变。棒状体参与刚地弓形虫的入侵及与宿主细胞的相互作用,并被认为是重要的毒力因子。在本研究中,我们构建了一种表达刚地弓形虫棒状体蛋白16(ROP16)的DNA疫苗,并评估了其在昆明小鼠体内诱导的免疫反应。将编码ROP16的基因序列插入真核表达载体pVAX I中。我们通过肌肉注射免疫昆明小鼠。免疫后,我们使用淋巴细胞增殖试验、细胞因子和抗体检测以及对致死性攻击小鼠的存活时间评估免疫反应。结果显示,与分别用空质粒或磷酸盐缓冲盐水免疫的其他小鼠相比,用pVAX - ROP16免疫的小鼠针对在大肠杆菌中表达的刚地弓形虫ROP16产生了高水平的特异性抗体反应、强烈的淋巴细胞增殖反应以及显著水平的γ干扰素(IFN -γ)、白细胞介素 - 2(IL - 2)、IL - 4和IL - 10分泌。结果表明,pVAX - ROP16诱导了显著的体液免疫和细胞Th1免疫反应。在致死性攻击后,与在攻击后7天内死亡的对照小鼠相比,用pVAX - ROP16免疫的小鼠存活时间显著延长(P < 0.05)(21.6 ± 9.9天)。我们的数据首次证明,ROP16引发了针对刚地弓形虫的强烈体液免疫和细胞免疫反应,并且ROP16是一种有前景的抗弓形虫病疫苗候选物,值得进一步开发。