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Construction and Phase I Clinical Evaluation of the Safety and Immunogenicity of a Candidate Enterotoxigenic Escherichia coli Vaccine Strain Expressing Colonization Factor Antigen CFA/I

机译:表达定殖因子抗原CFA / I的候选肠毒素大肠杆菌疫苗的安全性和免疫原性的构建和I期临床评价

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摘要

Oral delivery of toxin-negative derivatives of enterotoxigenic Escherichia coli (ETEC) that express colonization factor antigens (CFA) with deletions of the aroC, ompC, ompF, and toxin genes may be an effective approach to vaccination against ETEC-associated diarrhea. We describe the creation and characterization of an attenuated CFA/I-expressing ETEC vaccine candidate, ACAM2010, from a virulent isolate in which the heat-stable enterotoxin (ST) and CFA/I genes were closely linked and on the same virulence plasmid as the enteroaggregative E. coli heat-stable toxin (EAST1) gene. A new suicide vector (pJCB12) was constructed and used to delete the ST and EAST1 genes and to introduce defined deletion mutations into the aroC, ompC, and ompF chromosomal genes. A phase I trial, consisting of an open-label dose escalation phase in 18 adult outpatient volunteers followed by a placebo-controlled double-blind phase in an additional 31 volunteers, was conducted. The vaccine was administered in two formulations, fresh culture and frozen suspension. These were both well tolerated, with no evidence of significant adverse events related to vaccination. Immunoglobulin A (IgA) and IgG antibody-secreting cells specific for CFA/I were assayed by ELISPOT. Positive responses (greater than twofold increase) were seen in 27 of 37 (73%) subjects who received the highest dose level of vaccine (nominally 5 × 109 CFU). Twenty-nine of these volunteers were secreting culturable vaccine organisms at day 3 following vaccination; five were still positive on day 7, with a single isolation on day 13. This live attenuated bacterial vaccine is safe and immunogenic in healthy adult volunteers.
机译:口服表达表达定居因子抗原(CFA)并带有aroC,ompC,ompF和毒素基因缺失的肠毒素性大肠杆菌(ETEC)的毒素阴性衍生物可能是预防ETEC相关性腹泻的有效疫苗。我们描述了从强毒分离株(其中热稳定肠毒素(ST)和CFA / I基因紧密相连且在同一种毒力质粒上)的弱毒分离株中创建和表达减毒的表达CFA / I的ETEC疫苗候选物ACAM2010。肠聚合大肠杆菌热稳定毒素(EAST1)基因。构建了一个新的自杀载体(pJCB12),用于删除ST和EAST1基因,并将定义的缺失突变引入aroC,ompC和ompF染色体基因。进行了一项I期试验,该试验由18名成人门诊志愿者的开放剂量递增阶段组成,然后由另外31名志愿者进行的安慰剂对照双盲阶段组成。疫苗以两种制剂给药,即新鲜培养物和冷冻悬浮液。这些都耐受良好,没有证据表明与疫苗接种有关的重大不良事件。通过ELISPOT测定对CFA / I具有特异性的免疫球蛋白A(IgA)和分泌IgG抗体的细胞。在接受最高剂量疫苗接种(标称5×10 9 CFU)的37名受试者中,有27名(占73%)出现了阳性反应(增加了两倍以上)。这些志愿者中有29名在接种疫苗后的第3天分泌了可培养的疫苗生物。在第7天,有5例仍呈阳性,在第13天进行了一次隔离。这种减毒活疫苗在健康的成年志愿者中是安全且具有免疫原性的。

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