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Induction of humoral response following immunization with three different plasmid DNA vaccines against African trypanosomiasis

机译:三种不同质粒DNA疫苗免疫接种非洲锥虫病后诱导体液反应

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African Trypanosomiasis (AT) is a parasitic disease caused by the flagellated protozoan of the species Trypanosoma brucei. Currently the treatment used to combat AT is not satisfactory because the drugs used for the treatment are potentially toxic and often associated to important secondary effects. In this study, we show that Balb-C mice intramuscularly immunized with a single dose of plasmid encoding three antigenic candidate genes from Trypanosoma brucei, named Invariant Surface Glycoprotein (ISG), trans-sialidase (TSA), and Phospholipase C (PLC) are able to produce antibodies IgG anti-trypanosoma. This immunization process is herein shown as able to control the mortality level when mice were submitted to challenge assay with Trypanosoma brucei brucei parasites. Our results open up the possibility of the use of new attractive targets for vaccine development against AT.
机译:非洲锥虫瘤病(AT)是由物种Trypanosoma Brucei的鞭打原生动物引起的寄生疾病。目前,用于打击的治疗是不令人满意的,因为用于治疗的药物可能毒性,并且通常与重要的二次效果相关。在这项研究中,我们表明BALB-C小鼠用单剂量的质粒免疫,所述单剂量质粒从锥虫瘤Brucei中编码三种抗原候选基因,命名不变表面糖蛋白(ISG),反式唾液酸酶(TSA)和磷脂酶C(PLC)是能够产生抗体IgG抗锥体瘤。此免疫过程本文显示为能够控制小鼠的死亡率,当小鼠用睾丸瘤Brucei Brucei寄生虫攻击攻击测定时。我们的成果开辟了利用新有吸引力的疫苗发展目标的可能性。

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