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Trial of Infant Probiotic Exposure on Developing Asthma

Trial of Infant Probiotic Exposure on Developing Asthma
婴儿益生菌暴露对发生哮喘的试验
批准号:
7102572
负责人:
Michael D Cabana
金额:
$48.29万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-27 至 2009-06-30

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项目成果

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中文摘要
翻译
描述(由申请人提供):卫生假说表明内毒素暴露的缺失会导致不利的Th1/Th2平衡。在婴儿期控制抗原暴露可能有助于建立Th1/Th2平衡,从而阻止哮喘的发作或进展。乳酸菌是一种存在于典型儿科饮食中许多食物中的细菌,被用作预防腹泻的补充剂。由于乳杆菌在预防特应性皮炎方面的安全性、可行性和早期有希望的结果,乳杆菌是一种理想的细菌,可以用作检验卫生假设的暴露物。我们假设这样的暴露可能会阻碍或延缓哮喘早期标志物的发展。采用随机安慰剂对照试验设计,我们将测量6个月每日暴露乳酸菌作为婴儿配方奶粉补充剂对3岁前免疫系统和哮喘发展的影响。我们将测量抗原暴露对出现以下症状的影响:(1)哮喘发展的早期临床标志(频繁喘息、喘息无感冒、鼻炎和特应性皮炎);(2)哮喘发展的早期免疫标志物(嗜酸性粒细胞、IgE);(3)辅助性t表型(Th-1 vs Th-2)的发展。我们将通过测量全血淋巴细胞对兴奋剂的反应来表征Th表型,聚焦Th1 (ifn - γ, IL-12)和Th2细胞因子(IL-10, IL-4, IL-13),以及实时逆转录聚合酶链反应(RT-PCR)和PCR扩增(TaqMan)来量化RNA转录物。临床和免疫指标将被测量到3岁。依从性将通过日记、药片计数和乳酸杆菌粪便培养来评估。我们将使用意向治疗分析,并使用多变量回归和生存分析技术控制家庭、环境、饮食和人口因素对结果的影响。我们预计,与对照组相比,接受乳酸杆菌治疗的受试者哮喘标志物的发展将减少和延迟,Th1表型的可能性更大。
英文摘要
DESCRIPTION (provided by applicant): The hygiene hypothesis suggests that the absence of endotoxin exposure leads to an unfavorable Th1/Th2 balance. A controlled antigen exposure during infancy may help establish a Th1/Th2 balance that blocks the onset or progression of asthma. Lactobacillus is a bacterium found in many foods in the typical pediatric diet, and is used as a supplement to prevent diarrhea. Due to the safety, feasibility and early promising results in preventing atopic dermatitis, Lactobacillus is an ideal bacterium to use as an exposure to test the hygiene hypothesis. We hypothesize that such an exposure may block or delay development of early markers of asthma. Using a randomized placebo-controlled trial design, we will measure the effect of a 6-month daily exposure of Lactobacillus, as an infant formula supplement, on immune system and asthma development during the first 3 years of life. We will measure the effect of the antigen exposure on the presence and time to presentation of (1) early clinical markers for asthma development (frequent wheezing, wheezing without colds, rhinitis, and atopic dermatitis); (2) early immunologic markers for asthma development (eosinophilia, IgE); and (3) development of a T-helper phenotype (Th-1 vs Th-2). We will characterize the Th phenotype by measuring the whole blood lymphocyte response to stimulants, focusing Th1 (IFN-gamma, IL-12) and Th2 cytokines (IL-10, IL-4, IL-13), as well as real-time reverse transcriptase polymerase chain reaction (RT-PCR) with PCR amplification (TaqMan) to quantify RNA transcripts. Clinical and immunologic markers will be measured up to 3 years of age. Adherence will be assessed using diaries, pill count, and Lactobacillus stool cultures. We will use intention-to-treat analysis and will control for the impact of family, environmental, diet, and demographic factors on outcomes using multivariate regression and survival analysis techniques. We expect that when compared to controls, subjects receiving Lactobacillus will have decreased and delayed development of markers for asthma, and a greater likelihood of developing a Th1 phenotype.
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