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柴油尾气颗粒及其相关多环芳烃在过敏性气道疾病诱发中的作用。

The role of diesel exhaust particles and their associated polyaromatic hydrocarbons in the induction of allergic airway disease.

作者信息

Diaz-Sanchez D

机构信息

Division of Clinical Immunology and Allergy, University of California Los Angeles School of Medicine 90024-1680, USA.

出版信息

Allergy. 1997;52(38 Suppl):52-6; discussion 57-8. doi: 10.1111/j.1398-9995.1997.tb04871.x.

Abstract

The increase in allergic airway disease has paralleled the increase in the use of fossil fuels. Studies were undertaken to examine whether extracts of polyaromatic hydrocarbons (PAH) from diesel exhaust particles (DEP) (PAH-DEP) acted as mucosal adjuvants to help initiate or enhance immunoglobulin E (IgE) production in response to common inhaled allergens. In vitro studies demonstrated that PAH-DEP enhanced IgE production by tonsillar B-cells in the presence of interleukin-4 (IL-4) and CD40 monoclonal antibody, and altered the nature of the IgE produced, i.e. a decrease in the CH4'-CHe5 variant, a marker for differentiation of IgE-producing B-cells, and an increase in the M2' variant. In vivo nasal provocation studies using 0.30 mg DEP in saline also showed enhanced IgE production in the human upper respiratory mucosa, accompanied by a reduced CH4'-CHe5 mRNA splice variant. The effects of DEP were also isotype-specific, with no effect on IgG, IgA, IgM, or albumin, but it produced a small increase in the IgG4 subclass. The ability of DEP to act as an adjuvant to the ragweed allergen Amb a I was examined by nasal provocation in ragweed allergic subjects using 0.3 mg DEP, Amb a I, or both. Although allergen and DEP each enhanced ragweed-specific IgE, DEP plus allergen promoted a 16-times greater antigen-specific IgE production. Nasal challenge with DEP also influenced cytokine production. Ragweed challenge resulted in a weak response, DEP challenge caused a strong but non-specific response, while allergen plus DEP caused a significant increase in the expression of mRNA for TH0 and TH2-type cytokines (IL-4, IL-5, IL-6, IL-10, IL-13) with a pronounced inhibitory effect on IFN-gamma gene expression. These studies suggest that DEP can enhance B-cell differentiation, and by initiating and elevating IgE production, may play an important role in the increased incidence of allergic airway disease.

摘要

变应性气道疾病的增加与化石燃料使用的增加是同步的。开展了多项研究,以检验柴油废气颗粒(DEP)中的多环芳烃(PAH)提取物(PAH-DEP)是否作为黏膜佐剂,帮助启动或增强针对常见吸入性变应原的免疫球蛋白E(IgE)产生。体外研究表明,在白细胞介素-4(IL-4)和CD40单克隆抗体存在的情况下,PAH-DEP增强了扁桃体B细胞的IgE产生,并改变了所产生IgE的性质,即产生IgE的B细胞分化标志物CH4'-CHe5变体减少,而M2'变体增加。在体内,使用盐水中0.30 mg DEP进行鼻腔激发试验也显示,人上呼吸道黏膜中的IgE产生增强,同时CH4'-CHe5 mRNA剪接变体减少。DEP的作用也是同型特异性的,对IgG、IgA、IgM或白蛋白无影响,但使IgG4亚类略有增加。通过在豚草过敏受试者中使用0.3 mg DEP、豚草变应原Amb a I或两者进行鼻腔激发试验,检验了DEP作为豚草变应原Amb a I佐剂的能力。虽然变应原和DEP各自增强了豚草特异性IgE,但DEP加变应原促进了抗原特异性IgE产生增加16倍。用DEP进行鼻腔激发也影响细胞因子的产生。豚草激发导致微弱反应,DEP激发引起强烈但非特异性反应,而变应原加DEP导致TH0和TH2型细胞因子(IL-4、IL-5、IL-6、IL-10、IL-13)的mRNA表达显著增加,对IFN-γ基因表达有明显抑制作用。这些研究表明,DEP可增强B细胞分化,并通过启动和提高IgE产生,可能在变应性气道疾病发病率增加中起重要作用。

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