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Construction and Characterization of Genetically Defined aro omp Mutants of Enterotoxigenic Escherichia coli and Preliminary Studies of Safety and Immunogenicity in Humans

机译:产肠毒素大肠埃希氏菌的遗传定义芳香突变体的构建和表征以及人类安全性和免疫原性的初步研究

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摘要

Enterotoxigenic Escherichia coli (ETEC) is a leading cause of diarrhea in travelers to countries where the disease is endemic and causes a major disease burden in the indigenous population, particularly children. We describe here the generation and preclinical characterization of candidate strains of ETEC which are intended to provide the basis of a live attenuated oral vaccine to prevent this disease. It has been shown previously that a spontaneously arising toxin-negative variant ETEC strain, E1392/75-2A, could confer 75% protection against challenge when administered to volunteers. Unfortunately this strain induced mild diarrhea in 15% of recipients. To eliminate the unacceptable reactogenicity of strain E1392/75-2A, it was further attenuated by introducing three different combinations of defined deletion mutations into the chromosome. A mouse intranasal model of immunization was developed and used to show that all of the strains were immunogenic. Immune responses against colonization factor antigens (CFAs) were particularly strong when the bacterial inocula were grown on “CFA agar,” which induces strong expression of these antigens. Two of the strains were selected for a phase I dose escalation safety study with healthy adult volunteers. Freshly grown organisms were harvested from CFA agar plates and administered to volunteers as a suspension containing from 5 × 107 to 5 × 109 CFU. The vaccine was well tolerated at all doses and induced significant immune responses in all recipients at the highest dose of either strain. The results provide the basis for further clinical evaluation of these vaccine candidates.
机译:产肠毒素的大肠杆菌(ETEC)是前往该病流行国家的旅行者腹泻的主要原因,并给土著居民,特别是儿童造成重大疾病负担。我们在这里描述了ETEC候选菌株的产生和临床前表征,旨在为减毒口服活疫苗提供基础,以预防这种疾病。先前已显示,当施用于志愿者时,自发产生的毒素阴性变异ETEC株E1392 / 75-2A可以赋予75%的抗攻击保护。不幸的是,该菌株在15%的接受者中引起了轻度腹泻。为消除菌株E1392 / 75-2A的不可接受的反应原性,可通过将定义的缺失突变的三种不同组合引入染色体来进一步减弱。建立了小鼠鼻内免疫模型,并用于显示所有菌株均具有免疫原性。当细菌接种物在“ CFA琼脂”上生长时,对定殖因子抗原(CFA)的免疫反应特别强烈,这会诱导这些抗原的强表达。选择了其中两个菌株与健康成人志愿者进行I期剂量递增安全性研究。从CFA琼脂平板上收获新鲜生长的生物,并以包含5×10 7 至5×10 9 CFU的悬浮液的形式施用于志愿者。该疫苗在所有剂量下均具有良好的耐受性,并且在任一菌株的最高剂量下均可在所有接受者中引起明显的免疫反应。结果为这些候选疫苗的进一步临床评估提供了基础。

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