Ng Nicholas, Lam Diane, Paulus Petra, Batzer Glenda, Horner Anthony A
Department of Medicine, University of California, San Diego, La Jolla 92093-0663, USA.
J Allergy Clin Immunol. 2006 May;117(5):1074-81. doi: 10.1016/j.jaci.2006.03.025.
Although mechanisms remain a subject of controversy, there is general agreement that living environments influence allergic risk during the first years of life. We reasoned that sterile house dust extracts (HDEs) would have immunologic activities reflective of their environments of origin and therefore would be useful surrogates for investigations of how ambient exposures influence immune homeostasis.
These experiments determined how airway HDE exposures influence adaptive responses to a coadministered antigen and subsequent airway hypersensitivity responses to antigen challenge.
Mice received intranasal ovalbumin (OVA) vaccinations on a weekly basis. Select groups of mice also received intranasal HDE weekly with OVA; daily at one seventh the weekly dose, beginning 7 days before the first OVA sensitization; or both.
Weekly intranasal vaccinations with OVA and HDE primed mice for the development of T(H)2-biased immune and airway hypersensitivity responses. In contrast, daily low-dose intranasal HDE exposures protected against the immunologic and pathologic outcomes associated with weekly intranasal OVA/HDE vaccinations. The T(H)2 adjuvant activities of HDEs were found to be dependant on MyD88, a molecule critical for signaling through a majority of Toll-like receptors. Moreover, the tolerogenic activity associated with daily intranasal HDE exposures could be replicated with LPS.
These investigations demonstrate that in addition to allergens, living environments contain immunomodulatory materials with both T(H)2 adjuvant and tolerogenic activities.
As the contents of HDEs are ubiquitous, these experiments might recapitulate and help explain clinically relevant immunologic events involved in the maintenance of aeroallergen tolerance and the dysregulated responses that lead to allergic respiratory diseases.
尽管其机制仍存在争议,但人们普遍认为生活环境会影响生命最初几年的过敏风险。我们推测无菌屋尘提取物(HDE)具有反映其来源环境的免疫活性,因此将是研究环境暴露如何影响免疫稳态的有用替代物。
这些实验确定了气道暴露于HDE如何影响对共同给予抗原的适应性反应以及随后对抗原攻击的气道超敏反应。
小鼠每周接受鼻内卵清蛋白(OVA)疫苗接种。部分小鼠组在接种OVA的同时每周还接受鼻内HDE;从第一次OVA致敏前7天开始,每日给予每周剂量的七分之一;或两者同时给予。
每周鼻内接种OVA和HDE使小鼠易于发生偏向于辅助性T细胞2(TH2)的免疫和气道超敏反应。相比之下,每日低剂量鼻内暴露于HDE可预防与每周鼻内接种OVA/HDE相关的免疫和病理结果。发现HDE的TH2佐剂活性依赖于髓样分化因子88(MyD88),这是一种对通过大多数Toll样受体进行信号传导至关重要的分子。此外,每日鼻内暴露于HDE相关的免疫耐受活性可用脂多糖复制。
这些研究表明,除过敏原外,生活环境还含有具有TH2佐剂和免疫耐受活性的免疫调节物质。
由于HDE的成分无处不在,这些实验可能概括并有助于解释与维持空气过敏原耐受性以及导致过敏性呼吸道疾病的反应失调相关的临床相关免疫事件。