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Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study.发展中国家婴幼儿腹泻疾病负担和病因学(全球肠道发病和生存研究,GEMS):一项前瞻性、病例对照研究。
Lancet. 2013 Jul 20;382(9888):209-22. doi: 10.1016/S0140-6736(13)60844-2. Epub 2013 May 14.
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Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010.1990年和2010年20个年龄组中235种死因的全球和区域死亡率:全球疾病负担研究2010的系统分析
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A challenge model for Shigella dysenteriae 1 in cynomolgus monkeys (Macaca fascicularis).食蟹猴(猕猴属)中痢疾志贺氏菌1型的攻毒模型。
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Safety and colonization of two novel VirG(IcsA)-based live Shigella sonnei vaccine strains in rhesus macaques (Macaca mulatta).两种基于VirG(IcsA)的新型宋内志贺氏菌活疫苗株在恒河猴(猕猴)中的安全性和定殖情况。
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Capsule polysaccharide conjugate vaccine against diarrheal disease caused by Campylobacter jejuni.针对空肠弯曲菌引起的腹泻病的荚膜多糖结合疫苗。
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Shigella sonnei outbreak among homosexual men, London.伦敦男同性恋者中宋内志贺菌暴发。
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8
Epidemiology and genetic characterization of Shigella flexneri strains isolated from three paediatric populations in Egypt (2000-2004).从埃及三个儿科人群中分离出的福氏志贺氏菌菌株的流行病学及基因特征分析(2000 - 2004年)
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Incidence, etiology, and impact of diarrhea among long-term travelers (US military and similar populations): a systematic review.长期旅行者(美国军人及类似人群)腹泻的发病率、病因及影响:一项系统综述
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A recurring outbreak of Shigella sonnei among traditionally observant Jewish children in New York City: the risks of daycare and household transmission.纽约市传统犹太教儿童中宋内志贺菌反复暴发:日托和家庭传播的风险
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建立大食蚁兽(Aotus nancymaae)模型用于志贺氏菌疫苗免疫原性和功效研究。

Development of an Aotus nancymaae model for Shigella Vaccine immunogenicity and efficacy studies.

机构信息

U.S. Naval Medical Research Unit No. 6 (NAMRU-6), Callao, Peru.

出版信息

Infect Immun. 2014 May;82(5):2027-36. doi: 10.1128/IAI.01665-13. Epub 2014 Mar 4.

DOI:10.1128/IAI.01665-13
PMID:24595138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3993435/
Abstract

Several animal models exist to evaluate the immunogenicity and protective efficacy of candidate Shigella vaccines. The two most widely used nonprimate models for vaccine development include a murine pulmonary challenge model and a guinea pig keratoconjunctivitis model. Nonhuman primate models exhibit clinical features and gross and microscopic colonic lesions that mimic those induced in human shigellosis. Challenge models for enterotoxigenic Escherichia coli (ETEC) and Campylobacter spp. have been successfully developed with Aotus nancymaae, and the addition of a Shigella-Aotus challenge model would facilitate the testing of combination vaccines. A series of experiments were designed to identify the dose of Shigella flexneri 2a strain 2457T that induces an attack rate of 75% in the Aotus monkey. After primary challenge, the dose required to induce an attack rate of 75% was calculated to be 1 × 10(11) CFU. Shigella-specific immune responses were low after primary challenge and subsequently boosted upon rechallenge. However, preexisting immunity derived from the primary challenge was insufficient to protect against the homologous Shigella serotype. A successive study in A. nancymaae evaluated the ability of multiple oral immunizations with live-attenuated Shigella vaccine strain SC602 to protect against challenge. After three oral immunizations, animals were challenged with S. flexneri 2a 2457T. A 70% attack rate was demonstrated in control animals, whereas animals immunized with vaccine strain SC602 were protected from challenge (efficacy of 80%; P = 0.05). The overall study results indicate that the Shigella-Aotus nancymaae challenge model may be a valuable tool for evaluating vaccine efficacy and investigating immune correlates of protection.

摘要

存在几种动物模型可用于评估候选志贺氏菌疫苗的免疫原性和保护效力。两种最广泛用于疫苗开发的非灵长类动物模型包括鼠类肺部攻毒模型和豚鼠角膜结膜炎模型。非人类灵长类动物模型表现出的临床特征和大体及显微镜下的结肠病变与人类志贺氏菌病诱导的病变相似。已经成功地使用南迪猕猴建立了肠产毒性大肠杆菌(ETEC)和弯曲菌属挑战模型,添加志贺氏菌-南迪猕猴挑战模型将有助于测试联合疫苗。设计了一系列实验来确定诱导南迪猕猴攻击率为 75%的福氏志贺氏菌 2a 株 2457T 的剂量。初次攻毒后,计算出诱导攻击率为 75%所需的剂量为 1×10(11)CFU。初次攻毒后志贺氏菌特异性免疫反应较低,随后再攻毒时增强。然而,初次攻毒产生的固有免疫力不足以保护免受同源志贺氏菌血清型的攻击。南迪猕猴中的一项后续研究评估了多次口服免疫活减毒志贺氏菌疫苗株 SC602 以抵抗攻毒的能力。经过三次口服免疫后,用福氏志贺氏菌 2a 2457T 对动物进行攻毒。对照组动物的攻击率为 70%,而用疫苗株 SC602 免疫的动物则受到保护而免受攻毒(效力为 80%;P=0.05)。总的研究结果表明,志贺氏菌-南迪猕猴攻毒模型可能是评估疫苗效力和研究保护免疫相关性的有用工具。