首页> 外文期刊>PLOS Neglected Tropical Diseases >Protective immune responses against Schistosoma mansoni infection by immunization with functionally active gut-derived cysteine peptidases alone and in combination with glyceraldehyde 3-phosphate dehydrogenase
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Protective immune responses against Schistosoma mansoni infection by immunization with functionally active gut-derived cysteine peptidases alone and in combination with glyceraldehyde 3-phosphate dehydrogenase

机译:通过功能性肠源性半胱氨酸肽酶单独或与3-磷酸甘油醛脱氢酶联用进行免疫,以抵抗曼氏血吸虫感染的保护性免疫应答

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Background Schistosomiasis, a severe disease caused by parasites of the genus Schistosoma, is prevalent in 74 countries, affecting more than 250 million people, particularly children. We have previously shown that the Schistosoma mansoni gut-derived cysteine peptidase, cathepsin B1 (SmCB1), administered without adjuvant, elicits protection (>60%) against challenge infection of S. mansoni or S. haematobium in outbred, CD-1 mice. Here we compare the immunogenicity and protective potential of another gut-derived cysteine peptidase, S. mansoni cathepsin L3 (SmCL3), alone, and in combination with SmCB1. We also examined whether protective responses could be boosted by including a third non-peptidase schistosome secreted molecule, glyceraldehyde 3-phosphate dehydrogenase (SG3PDH), with the two peptidases.
机译:背景技术血吸虫病是一种由血吸虫属寄生虫引起的严重疾病,在74个国家中普遍存在,影响了超过2.5亿人,特别是儿童。我们以前已经证明,曼氏血吸虫肠源性半胱氨酸肽酶组织蛋白酶B1(SmCB1)在没有佐剂的情况下给药,可在交配的CD-1小鼠中获得抗曼氏沙门氏菌或血生沙门氏菌挑战性感染的保护作用(> 60%)。在这里,我们比较了另一种肠道来源的半胱氨酸肽酶S. mansoni组织蛋白酶L3(SmCL3)单独和与SmCB1组合的免疫原性和保护潜力。我们还检查了是否可以通过将第三个非肽酶血吸虫分泌分子,甘油醛3-磷酸脱氢酶(SG3PDH)与两个肽酶一起加入来增强保护反应。

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