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吸入性环境过敏原和毒物作为哮喘表型的决定因素。

Inhaled environmental allergens and toxicants as determinants of the asthma phenotype.

机构信息

Division of Allergy and Immunology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX, 77555, USA,

出版信息

Adv Exp Med Biol. 2014;795:43-73. doi: 10.1007/978-1-4614-8603-9_4.

Abstract

The driving environmental factors behind the development of the asthma phenotype remain incompletely studied and understood. Here, we present an overview of inhaled allergic/atopic and mainly nonallergic/nonatopic or toxicant shapers of the asthma phenotype, which are present in both the indoor and outdoor environment around us. The inhaled allergic/atopic factors include fungus, mold, animal dander, cockroach, dust mites, and pollen; these allergic triggers and shapers of the asthma phenotype are considered in the context of their ability to drive the immunologic IgE response and potentially induce interactions between the innate and adaptive immune responses, with special emphasis on the NADPH-dependent reactive oxygen-species-associated mechanism of pollen-associated allergy induction. The inhaled nonallergic/nonatopic, toxicant factors include gaseous and volatile agents, such as sulfur dioxide, ozone, acrolein, and butadiene, as well as particulate agents, such as rubber tire breakdown particles, and diesel exhaust particles. These toxicants are reviewed in terms of their relevant chemical characteristics and hazard potential, ability to induce airway dysfunction, and potential for driving the asthma phenotype. Special emphasis is placed on their interactive nature with other triggers and drivers, with regard to driving the asthma phenotype. Overall, both allergic and nonallergic environmental factors can interact to acutely exacerbate the asthma phenotype; some may also promote its development over prolonged periods of untreated exposure, or possibly indirectly through effects on the genome. Further therapeutic considerations should be given to these environmental factors when determining the best course of personalized medicine for individuals with asthma.

摘要

导致哮喘表型发展的驱动环境因素仍不完全被研究和理解。在这里,我们概述了吸入性变应原/特应性和主要非变应原/非特应性或毒物性哮喘表型形成因子,这些因子存在于我们周围的室内和室外环境中。吸入性变应原/特应性因子包括真菌、霉菌、动物皮屑、蟑螂、尘螨和花粉;这些变应原触发因子和哮喘表型形成因子被认为是其能够驱动免疫 IgE 反应并潜在地诱导先天免疫和适应性免疫反应之间相互作用的能力,特别强调花粉相关过敏诱导中 NADPH 依赖性活性氧相关机制。吸入性非变应原/非特应性、毒物性因子包括气态和挥发性物质,如二氧化硫、臭氧、丙烯醛和丁二烯,以及颗粒性物质,如橡胶轮胎分解颗粒和柴油废气颗粒。这些毒物根据其相关的化学特性和危害潜力、诱导气道功能障碍的能力以及潜在的驱动哮喘表型的能力进行了综述。特别强调了它们与其他触发因素和驱动因素的相互作用,以驱动哮喘表型。总的来说,变应原和非变应原环境因素都可以相互作用,使哮喘表型急性恶化;一些因素也可能通过对基因组的间接影响,在未经治疗的暴露延长期间促进其发展。在确定个体化治疗方案时,应进一步考虑这些环境因素,以确定哮喘患者的最佳治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d163/9116436/1ea0ee1804d5/nihms-1011625-f0001.jpg

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