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首页> 外文期刊>BMC Infectious Diseases >Protective efficacy of Toxoplasma gondii calcium-dependent protein kinase 1 (TgCDPK1) adjuvated with recombinant IL-15 and IL-21 against experimental toxoplasmosis in mice
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Protective efficacy of Toxoplasma gondii calcium-dependent protein kinase 1 (TgCDPK1) adjuvated with recombinant IL-15 and IL-21 against experimental toxoplasmosis in mice

机译:重组IL-15和IL-21修饰的弓形虫钙依赖蛋白激酶1(TgCDPK1)对小鼠弓形虫的保护作用。

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Background Toxoplasma gondii can infect all warm-blooded animals including humans. Infection with T. gondii is probably the leading cause of posterior uveitis in humans and the most comment route of transmission is raw and undercooked meat from infected animals. T. gondii calcium-dependent protein kinase 1 (TgCDPK1) plays a critical role in direct parasite motility, host-cell invasion, and egress. Methods We constructed a DNA vaccine expressing TgCDPK1 inserted into eukaryotic expression vector pVAX I and evaluated the immune protection induced by pVAX-CDPK1 in Kunming mice. Mice immunized with pVAX-CDPK1 intramuscularly and/or with a plasmid encoding IL-15 and IL-21 (pVAX-IL-21-IL-15). The immune responses were analyzed including lymphoproliferative assay, cytokine, antibody measurements, lymphocyte surface markers by flow cytometry and protective efficacy were measured as survival and cysts numbers after challenge 1 to 2?months post vaccination. Results Immunization with pVAX-CDPK1 or pVAX-IL-21-IL-15 alone developed strong humoral responses and Th1 type cellular immune responses, and the significantly (P?P? Conclusions TgCDPK1 is identified to be a promising vaccine candidate for inducing a strong humoral and cellular response against T. gondii infection, and thus synergistic of mIL-21 and mIL-15 can induce non-specific immune responses, but also facilitate specific humoral as well as cellular immune responses elicited by DNA vaccine against acute and chronic T. gondii infection in mice.
机译:背景弓形虫可以感染包括人类在内的所有温血动物。弓形虫的感染可能是人类后葡萄膜炎的主要原因,传播的最途径是感染动物的生肉和未煮熟的肉。刚地弓形虫钙依赖性蛋白激酶1(TgCDPK1)在直接寄生虫运动,宿主细胞入侵和流出中起关键作用。方法我们构建了一种表达TgCDPK1的DNA疫苗,该疫苗已插入真核表达载体pVAX I中,并评估了pVAX-CDPK1对昆明小鼠的免疫保护作用。肌肉内用pVAX-CDPK1和/或编码IL-15和IL-21的质粒(pVAX-IL-21-IL-15)免疫的小鼠。分析免疫应答,包括淋巴增生测定,细胞因子,抗体测量,通过流式细胞术检测淋巴细胞表面标志物,并在接种疫苗后1至2个月后测定存活率和囊肿数,以保护作用。结果单独用pVAX-CDPK1或pVAX-IL-21-IL-15免疫可产生强烈的体液应答和Th1型细胞免疫应答,并且显着的免疫应答(P?P?结论)TgCDPK1被认为是诱导强力免疫的有希望的候选疫苗针对弓形虫感染的体液和细胞反应,因此mIL-21和mIL-15的协同作用可诱导非特异性免疫反应,但也促进针对急性和慢性T的DNA疫苗引发的特异性体液和细胞免疫反应。小鼠感染弓形虫。

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