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用编码刚地弓形虫棒状体蛋白17的基因进行DNA疫苗接种可诱导小鼠对致死性攻击产生部分保护性免疫。

DNA vaccination with a gene encoding Toxoplasma gondii Rhoptry Protein 17 induces partial protective immunity against lethal challenge in mice.

作者信息

Wang Hai-Long, Wang Yu-Jing, Pei Yan-Jiang, Bai Ji-Zhong, Yin Li-Tian, Guo Rui, Yin Guo-Rong

机构信息

Research Institute of Medical Parasitology, Shanxi Medical University, Taiyuan, Shanxi 030001, PR China.

Department of Biochemistry and Molecular Biology, Shanxi Medical University, Taiyuan, Shanxi 030001, PR China.

出版信息

Parasite. 2016;23:4. doi: 10.1051/parasite/2016004. Epub 2016 Feb 3.

Abstract

Toxoplasma gondii is an obligate intracellular apicomplexan parasite that affects humans and various vertebrate livestock and causes serious economic losses. To develop an effective vaccine against T. gondii infection, we constructed a DNA vaccine encoding the T. gondii rhoptry protein 17 (TgROP17) and evaluated its immune protective efficacy against acute T. gondii infection in mice. The DNA vaccine (p3×Flag-CMV-14-ROP17) was intramuscularly injected to BALB/c mice and the immune responses of the vaccinated mice were determined. Compared to control mice treated with empty vector or PBS, mice immunized with the ROP17 vaccine showed a relatively high level of specific anti-T. gondii antibodies, and a mixed IgG1/IgG2a response with predominance of IgG2a production. The immunized mice also displayed a specific lymphocyte proliferative response, a Th1-type cellular immune response with production of IFN-γ and interleukin-2, and increased number of CD8(+) T cells. Immunization with the ROP17 DNA significantly prolonged the survival time (15.6 ± 5.4 days, P < 0.05) of mice after challenge infection with the virulent T. gondii RH strain (Type I), compared with the control groups which died within 8 days. Therefore, our data suggest that DNA vaccination with TgROP17 triggers significant humoral and cellular responses and induces effective protection in mice against acute T. gondii infection, indicating that TgROP17 is a promising vaccine candidate against acute toxoplasmosis.

摘要

刚地弓形虫是一种专性细胞内顶复门寄生虫,可感染人类及多种脊椎动物家畜,并造成严重的经济损失。为研发一种有效的抗刚地弓形虫感染疫苗,我们构建了一种编码刚地弓形虫棒状体蛋白17(TgROP17)的DNA疫苗,并评估了其对小鼠急性刚地弓形虫感染的免疫保护效果。将该DNA疫苗(p3×Flag-CMV-14-ROP17)肌肉注射到BALB/c小鼠体内,并测定接种疫苗小鼠的免疫反应。与用空载体或PBS处理的对照小鼠相比,用ROP17疫苗免疫的小鼠显示出相对较高水平的特异性抗刚地弓形虫抗体,以及以IgG2a产生为主的混合IgG1/IgG2a反应。免疫小鼠还表现出特异性淋巴细胞增殖反应、产生IFN-γ和白细胞介素-2的Th1型细胞免疫反应,以及CD8(+) T细胞数量增加。与在8天内死亡的对照组相比,用ROP17 DNA免疫显著延长了小鼠在感染强毒株刚地弓形虫RH株(I型)后的存活时间(15.6±5.4天,P<0.05)。因此,我们的数据表明,用TgROP17进行DNA疫苗接种可引发显著的体液和细胞反应,并在小鼠中诱导针对急性刚地弓形虫感染的有效保护,表明TgROP17是一种有前景的抗急性弓形虫病疫苗候选物。

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