Stiemsma Leah T, Turvey Stuart E
Department of Microbiology & Immunology, University of British Columbia, Vancouver, BC Canada ; BC Children's Hospital, Vancouver, BC Canada.
BC Children's Hospital, Vancouver, BC Canada ; Department of Pediatrics, University of British Columbia, Vancouver, BC Canada ; Department of Pediatrics, BC Children's Hospital, 950 West 28th Avenue, Vancouver, BC V5Z 4H4 Canada.
Allergy Asthma Clin Immunol. 2017 Jan 6;13:3. doi: 10.1186/s13223-016-0173-6. eCollection 2017.
Asthma is a chronic inflammatory immune disorder of the airways affecting one in ten children in westernized countries. The geographical disparity combined with a generational rise in prevalence, emphasizes that changing environmental exposures play a significant role in the etiology of this disease. The microflora hypothesis suggests that early life exposures are disrupting the composition of the microbiota and consequently, promoting immune dysregulation in the form of hypersensitivity disorders. Animal model research supports a role of the microbiota in asthma and atopic disease development. Further, these model systems have identified an early life critical window, during which gut microbial dysbiosis is most influential in promoting hypersensitivity disorders. Until recently this critical window had not been characterized in humans, but now studies suggest that the ideal time to use microbes as preventative treatments or diagnostics for asthma in humans is within the first 100 days of life. This review outlines the major mouse-model and human studies leading to characterization of the early life critical window, emphasizing studies analyzing the intestinal and airway microbiotas in asthma and atopic disease. This research has promising future implications regarding childhood immune health, as ultimately it may be possible to therapeutically administer specific microbes in early life to prevent the development of asthma in children.
哮喘是一种影响西方国家十分之一儿童的气道慢性炎症性免疫疾病。地理差异以及患病率的代际上升,都表明环境暴露的变化在该疾病的病因中起着重要作用。微生物群假说认为,早期生活暴露正在破坏微生物群的组成,从而以过敏症的形式促进免疫失调。动物模型研究支持微生物群在哮喘和特应性疾病发展中的作用。此外,这些模型系统已经确定了一个早期生命关键期,在此期间肠道微生物失调对促进过敏症最为有影响。直到最近,这个关键期在人类中还没有得到描述,但现在的研究表明,在人类中使用微生物作为哮喘预防治疗或诊断的理想时间是在生命的前100天内。这篇综述概述了导致早期生命关键期特征化的主要小鼠模型和人类研究,重点是分析哮喘和特应性疾病中肠道和气道微生物群的研究。这项研究对儿童免疫健康具有充满希望的未来意义,因为最终有可能在生命早期通过治疗性给予特定微生物来预防儿童哮喘的发生。