Lu Gang, Wang Lin, Zhou Aihua, Han Yali, Guo Jingjing, Song Pengxia, Zhou Huaiyu, Cong Hua, Zhao Qunli, He Shenyi
Department of Parasitology, Shandong University School of Medicine, Jinan, Shandong Province 250012, People's Republic of China.
Department of Pediatrics, Provincial Hospital Affiliated to Shandong University, Shandong University School of Medicine, Jinan, Shandong Province 250021, People's Republic of China.
Acta Trop. 2015 Jun;146:66-72. doi: 10.1016/j.actatropica.2015.03.013. Epub 2015 Mar 16.
Bioinformatics approaches were used to identify B-cell epitopes and T-cell epitopes on SAG5A protein. Compared to SAG1, SAG5A with good B-cell epitopes and T-cell epitopes had a potentiality to become a more successful vaccine against Toxoplasma gondii. Thereafter, SAG5A DNA vaccine was constructed successfully and was injected into mice with peptide to evaluate the immunoprotection. Compared to the control groups, the vaccine (DNA/peptide) could induce more effective cellular and humoral immune responses in immunized mice. Furthermore, a significant reduction of brain cyst was detected in the mice vaccinated with peptide (732±160), pSAG5A (815±197), or pSAG5A/peptide (436±174) compared by the mice injected by PBS (1260±241) or pEGFP-C1 (1350±268). The number of cysts in brains was 35% reduced in the mice immunized with DNA/peptide than in the control mice treated by PBS. The results indicated that the DNA vaccine encoding SAG5A significantly induced immune responses and enhanced protection against cysts of PRU strain, especially with the help of peptide.
采用生物信息学方法鉴定SAG5A蛋白上的B细胞表位和T细胞表位。与SAG1相比,具有良好B细胞表位和T细胞表位的SAG5A有潜力成为一种更成功的抗弓形虫疫苗。此后,成功构建了SAG5A DNA疫苗,并将其与肽一起注射到小鼠体内以评估免疫保护作用。与对照组相比,该疫苗(DNA/肽)能在免疫小鼠中诱导更有效的细胞免疫和体液免疫反应。此外,与注射PBS(1260±241)或pEGFP-C1(1350±268)的小鼠相比,用肽(732±160)、pSAG5A(815±197)或pSAG5A/肽(436±174)免疫的小鼠脑内囊肿明显减少。用DNA/肽免疫的小鼠脑内囊肿数量比用PBS处理的对照小鼠减少了35%。结果表明,编码SAG5A的DNA疫苗能显著诱导免疫反应,并增强对PRU株囊肿的保护作用,尤其是在肽的辅助下。