Han Yali, Zhou Aihua, Lu Gang, Zhao Guanghui, Sha Wenchao, Wang Lin, Guo Jingjing, Zhou Jian, Zhou Huaiyu, Cong Hua, He Shenyi
Department of Parasitology, Shandong University School of Medicine, Jinan, Shandong, 250012, P. R. China.
Department of Pediatrics, Provincial Hospital Affiliated to Shandong University, Shandong University School of Medicine, Jinan, Shandong, 250021, P. R. China.
Korean J Parasitol. 2017 Oct;55(5):505-512. doi: 10.3347/kjp.2017.55.5.505. Epub 2017 Oct 31.
Toxoplasma gondii cathepsin C proteases (TgCPC1, 2, and 3) are important for the growth and survival of T. gondii. In the present study, B-cell and T-cell epitopes of TgCPC1 were predicted using DNAstar and the Immune Epitope Database. A TgCPC1 DNA vaccine was constructed, and its ability to induce protective immune responses against toxoplasmosis in BALB/c mice was evaluated in the presence or absence of the adjuvant α-GalCer. As results, TgCPC1 DNA vaccine with or without adjuvant α-GalCer showed higher levels of IgG and IgG2a in the serum, as well as IL-2 and IFN-γ in the spleen compared to controls (PBS, pEGFP-C1, and α-Galcer). Upon challenge infection with tachyzoites of T. gondii (RH), pCPC1/α-Galcer immunized mice showed the longest survival among all the groups. Mice vaccinated with DNA vaccine without adjuvant (pCPC1) showed better protective immunity compared to other controls (PBS, pEGFP-C1, and α-Galcer). These results indicate that a DNA vaccine encoding TgCPC1 is a potential vaccine candidate against toxoplasmosis.
刚地弓形虫组织蛋白酶C蛋白酶(TgCPC1、2和3)对刚地弓形虫的生长和存活至关重要。在本研究中,使用DNAstar和免疫表位数据库预测了TgCPC1的B细胞和T细胞表位。构建了一种TgCPC1 DNA疫苗,并在存在或不存在佐剂α-GalCer的情况下,评估了其在BALB/c小鼠中诱导针对弓形虫病的保护性免疫反应的能力。结果显示,与对照组(PBS、pEGFP-C1和α-GalCer)相比,添加或不添加佐剂α-GalCer的TgCPC1 DNA疫苗在血清中显示出更高水平的IgG和IgG2a,以及在脾脏中显示出更高水平的IL-2和IFN-γ。在用刚地弓形虫(RH)速殖子进行攻击感染后,pCPC1/α-GalCer免疫的小鼠在所有组中存活时间最长。与其他对照组(PBS、pEGFP-C1和α-GalCer)相比,接种无佐剂DNA疫苗(pCPC1)的小鼠表现出更好的保护性免疫。这些结果表明,编码TgCPC1的DNA疫苗是一种潜在的抗弓形虫病疫苗候选物。