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The piglet acute diarrhea model for evaluating efficacy of treatment and control of cryptosporidiosis

机译:用于评估治疗疗效和控制隐孢子虫病疗效的仔猪急性腹泻模型

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摘要

Cryptosporidium spp. are ranked as the second leading pathogens causing life-threatening diarrhea in children under 2?years of age. Although Cryptosporidium hominis causes three quarters of the cases of cryptosporidiosis, studies on C. hominis are limited since natural disease due to C. hominis is host-restricted to humans only. In this mini-review, we demonstrate the successfully adoption, propagation, and utility of the C. hominis strain TU502, isolated originally from an infant with diarrhea in Uganda, in gnotobiotic piglets. The TU502 C. hominis strain and the gnotobiotic piglet model currently are the only available preclinical tools to evaluate therapeutics that specifically target C. hominis. Infection in this gnotobiotic piglet model displays similar clinical symptoms of diarrhea observed in humans. Here we further describe how this unique model of acute diarrhea, can be used for drug discovery and testing of vaccine candidates against cryptosporidiosis. The shared anatomical, physiological and immunological characteristics between piglets and human infants makes the model ideal for evaluating the efficacy of therapeutics and vaccines against cryptosporidiosis as they become available.
机译:Cryptosporidium spp。被评为第二种主要病原体,导致2岁以下儿童危及生命的腹泻。虽然Cryptosporidium hominis导致三个季度的隐孢子虫病病例,但C. hominis的研究由于C. hominis引起的自然疾病仅限于人类而受到限制。在这个迷你性审查中,我们证明了C. hominis菌株Tu502的成功采用,繁殖和效用,最初来自乌干达的婴儿的婴儿,在尿道仔猪。 TU502 C. hominis菌株和八卵茎仔猪模型目前是唯一可用的临床前工具,用于评估特异性靶向C. hominis的治疗方法。这种八噬菌素仔猪模型中的感染显示了人类观察到的腹泻的类似临床症状。在这里,我们进一步描述了这种急性腹泻的独特模型如何用于药物发现和对疫苗候选人的药物患者进行抗衰孔症。仔猪和人婴儿之间的共同解剖,生理和免疫学特征使得模型非常适合评估治疗和疫苗的疗效,因为它们变得可用。

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