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首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Evaluation of an intragastric challenge model for Shigella dysenteriae 1 in rhesus monkeys (Macaca mulatta) for the pre-clinical assessment of Shigella vaccine formulations
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Evaluation of an intragastric challenge model for Shigella dysenteriae 1 in rhesus monkeys (Macaca mulatta) for the pre-clinical assessment of Shigella vaccine formulations

机译:恒河猴(Macaca mulatta)痢疾志贺氏菌1胃内激发模型的评估,以对志贺氏菌疫苗制剂进行临床前评估

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摘要

Shigellosis is a worldwide disease, characterized by abdominal pain, fever, vomiting, and the passage of blood- and mucus-streaked stools. Rhesus monkeys and other primates are the only animals that are naturally susceptible to shigellosis. A suitable animal model is required for the pre-clinical evaluation of vaccines candidates. In this study, the minimal dose of Shigella dysenteriae1 1617 strain required to produce dysentery in four of five (80% attack rate) monkeys using an escalating dose range for three groups [2 × 108, 2 × 109 and 2 × 1010 colony forming unit (CFU)] was determined. In addition, the monkeys were re-infected. The identified optimal challenge dose was 2 × 109 CFU; this dose elicited 60% protection in monkeys when they were re-challenged with a one log higher dose (2 × 1010 CFU). The challenge dose, 2 × 1010 CFU, produced severe dysentery in all monkeys, with one monkey dying within 24 h, elicited 100% protection when re-challenged with the same dose. All monkeys exhibited immune responses. This study concludes that the rhesus monkey model closely mimics the disease and immune response seen in humans and is a suitable animal model for the pre-clinical evaluation of Shigella vaccine candidates. Prior infection with the 1617 strain can protect monkeys against subsequent re-challenges with homologous strains.
机译:志贺氏菌病是一种世界性疾病,其特征是腹痛,发烧,呕吐以及有血和黏液条纹的粪便通过。恒河猴和其他灵长类动物是唯一自然对志贺菌病敏感的动物。临床前评估候选疫苗需要合适的动物模型。在这项研究中,使用递增剂量范围的三组[2×108、2×109和2×1010集落形成单位],在五只猴子中有四只(80%攻击率)猴子产生痢疾所需的最低剂量的志贺氏菌dysenteriae1 1617菌株。 ((CFU)]。另外,猴子被再次感染。鉴定的最佳激发剂量为2×109 CFU。当用高一个对数的剂量(2×1010 CFU)再次挑战猴子时,该剂量在猴子中引起60%的保护。攻击剂量2×1010 CFU在所有猴子中产生严重的痢疾,其中一只猴子在24 h内死亡,当再次受到相同剂量的攻击时,可引起100%的保护。所有的猴子都表现出免疫反应。这项研究得出的结论是,恒河猴模型与人类所见的疾病和免疫反应密切相似,并且是对志贺氏菌疫苗候选者进行临床前评估的合适动物模型。事先用1617毒株感染可以保护猴子免于随后受到同源毒株的再次攻击。

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