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首页> 外文期刊>Vaccine >Antibody recognition of cathepsin L1-derived peptides in ce:italic>Fasciola hepatica/ce:italic>-infected and/or vaccinated cattle and identification of protective linear B-cell epitopes
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Antibody recognition of cathepsin L1-derived peptides in ce:italic>Fasciola hepatica/ce:italic>-infected and/or vaccinated cattle and identification of protective linear B-cell epitopes

机译:抗体识别& ce:斜体>粉碎蛋白肽中的蛋白酶蛋白酶L1衍生肽:斜体> - 射频> - 染色和/或疫苗接种的牛和保护性线性B细胞表位的鉴定

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摘要

Fasciola hepaticainfection causes important economic losses in livestock and food industries around the world. In the Republic of IrelandF. hepaticainfection has an 76% prevalence in cattle. Due to the increase of anti-helminthic resistance, a vaccine-based approach to control of Fasciolosis is urgently needed. A recombinant version of the cysteine protease cathepsin L1 (rmFhCL1) fromF. hepaticahas been a vaccine candidate for many years. We have found that vaccination of cattle with this immunodominant antigen has provided protection against infection in some experimental trials, but not in others. Differential epitope recognition between animals could be a source of variable levels of vaccine protection. Therefore, we have characterised for first time linear B-cell epitopes recognised within the FhCL1 protein using sera fromF. hepatica-infected and/or vaccinated cattle from two independent trials. Results showed that allF. hepaticainfected animals recognised the region 19–31 of FhCL1, which is situated in the N-terminal part of the pro-peptide. Vaccinated animals that showed fluke burden reduction elicited antibodies that bound to the regions 120–137, 145–155, 161–171 of FhCL1, which were not recognised by non-protected animals. This data, together with the high production of specific IgG2 in animals showing vaccine efficacy, suggest important targets for vaccine development.
机译:Fasciola肝脏喂食导致世界各地的家畜和食品工业中的重要经济损失。在爱尔兰共和国。肝脏在牛的患者中具有76%的患病率。由于抗蠕虫性抗性的增加,迫切需要抗蠕虫性抗性的疫苗控制方法,用于控制粘性菌病变。半胱氨酸蛋白酶组织蛋白酶L1(RMFHCL1)的重组版本。肝脏是多年来一直是疫苗候选人。我们发现牛与这种免疫模数抗原的疫苗接种在一些实验试验中提供了免受感染的保护,但不在其他试验中提供了保护。动物之间的差异表位识别可能是可变水平的疫苗保护源。因此,我们的特征在于使用血清FRFF在FHCL1蛋白内识别的第一时间线性B细胞表位。来自两个独立试验的肝脏感染和/或疫苗接种的牛。结果表明ALLF。肝癌动物认识到FHCL1的19-31区域,其位于Pro-peptide的N-末端部分。疫苗的动物,显示氟克解的引起的抗体,其与未受保护的动物不识别的FHCL1的区域120-137,1175,161-171。这种数据与出现疫苗疗效的动物的高产生特异性IgG2,表明疫苗发育的重要靶标。

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