首页> 外文期刊>The Lancet >Use of a patch containing heat-labile toxin from Escherichia coli against travellers' diarrhoea: a phase II, randomised, double-blind, placebo-controlled field trial.
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Use of a patch containing heat-labile toxin from Escherichia coli against travellers' diarrhoea: a phase II, randomised, double-blind, placebo-controlled field trial.

机译:含有来自大肠杆菌的不耐热毒素的贴剂对旅行者腹泻的用途:II期,随机,双盲,安慰剂对照的田间试验。

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BACKGROUND: Enterotoxigenic Escherichia coli (ETEC) is a major cause of travellers' diarrhoea. We investigated the rate of diarrhoea attacks, safety, and feasibility of a vaccine containing heat-labile enterotoxin (LT) from ETEC delivered to the skin by patch in travellers to Mexico and Guatemala. METHODS: In this phase II study, healthy adults (aged 18-64 years) who planned to travel to Mexico or Guatemala and had access to a US regional vaccination centre were eligible. A centralised randomisation code was used for allocation, which was masked to participants and site staff. Primary endpoints were to investigate the field rate of ETEC diarrhoea, and to assess the safety of heat-labile toxins from E coli (LT) delivered via patch. Secondary endpoints included vaccine efficacy against travellers' diarrhoea and ETEC. Participants were vaccinated before travel, with two patches given 2-3 weeks apart. Patches contained either 37.5 mug of LT or placebo. Participants tracked stool output on diary cards in country and provided samples for pathogen identification if diarrhoea occurred. Diarrhoea was graded by the number of loose stools in 24 h: mild (three), moderate (four or five), and severe (at least six). Analysis was per protocol. The trial is registered with ClinicalTrials.gov, number NCT00516659. FINDINGS: Recruitment closed after 201 participants were assigned patches. 178 individuals received two vaccinations and travelled and 170 were analysed. 24 (22%) of 111 placebo recipients had diarrhoea, of whom 11 (10%) had ETEC diarrhoea. The vaccine was safe and immunogenic. The 59 LT-patch recipients were protected against moderate-to-severe diarrhoea (protective efficacy [PE] 75%, p=0.0070) and severe diarrhoea (PE 84%, p=0.0332). LT-patch recipients who became ill had shorter episodes of diarrhoea (0.5 days vs 2.1 days, p=0.0006) with fewer loose stools (3.7 vs 10.5, p<0.0001) than placebo. INTERPRETATION: Travellers' diarrhoea is a common ailment, with ETEC diarrhoea illness occurring in 10% of cases. The vaccine patch is safe and feasible, with benefits to the rate and severity of travellers' diarrhoea.
机译:背景:产肠毒素大肠杆菌(ETEC)是旅行者腹泻的主要原因。我们调查了腹泻发作的速度,安全性和一种疫苗的可行性,该疫苗包含从ETEC运送至皮肤和墨西哥的危地马拉旅行者从皮肤中提取的不耐热肠毒素(LT)。方法:在此II期研究中,计划前往墨西哥或危地马拉并可以进入美国区域疫苗接种中心的健康成年人(年龄18-64岁)是合格的。使用集中的随机化代码进行分配,该代码对参与者和现场人员隐蔽。主要终点是调查ETEC腹泻的田间发生率,并评估通过贴片输送的来自大肠杆菌(LT)的热不稳定毒素的安全性。次要终点包括疫苗对旅行者腹泻和ETEC的功效。参与者在旅行前进行了疫苗接种,两次贴片间隔2-3周。补丁包含37.5杯LT或安慰剂。参加者在国家的日记卡上跟踪粪便的排出量,并提供样本以用于在发生腹泻时进行病原体鉴定。腹泻按24小时内稀便的数量进行分级:轻度(3次),中度(4或5次)和重度(至少6次)。根据方案进行分析。该试验已在ClinicalTrials.gov上注册,编号为NCT00516659。结果:在为201位参与者分配了补丁之后,招募活动关闭。 178人接受了两次疫苗接种并旅行,并对170人进行了分析。 111位安慰剂接受者中有24位(22%)患有腹泻,其中11位(10%)患有ETEC腹泻。该疫苗安全且具有免疫原性。 59位LT贴剂接受者可预防中度至重度腹泻(保护功效[PE] 75%,p = 0.0070)和严重腹泻(PE 84%,p = 0.0332)。与安慰剂相比,生病的LT贴片的腹泻发作时间较短(0.5天vs 2.1天,p = 0.0006),大便稀少(3.7 vs 10.5,p <0.0001)。解释:旅行者的腹泻是一种常见疾病,其中10%的病例发生ETEC腹泻病。该疫苗贴片安全可行,对旅行者腹泻的发生率和严重程度都有好处。

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