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使用偏苯三酸酐(一种呼吸道致敏剂)和二硝基氯苯(一种皮肤致敏剂)对化学诱导性哮喘小鼠模型进行验证。

Validation of a mouse model of chemical-induced asthma using trimellitic anhydride, a respiratory sensitizer, and dinitrochlorobenzene, a dermal sensitizer.

作者信息

Vanoirbeek Jeroen A J, Tarkowski Maciej, Vanhooren Hadewijch M, De Vooght Vanessa, Nemery Benoit, Hoet Peter H M

机构信息

Laboratory of Pneumology, Unit of Lung Toxicology, Katholieke Universiteit Leuven, Leuven, Belgium.

出版信息

J Allergy Clin Immunol. 2006 May;117(5):1090-7. doi: 10.1016/j.jaci.2006.01.027. Epub 2006 Mar 3.

Abstract

BACKGROUND

Occupational asthma can be caused by chemicals. Previously, we established a murine model of immunologically mediated chemical-induced asthma using toluene diisocyanate.

OBJECTIVE

We sought to verify this model using trimellitic anhydride (TMA), a respiratory sensitizer, and 1-chloro-2,4-dinitrobenzene (DNCB), a dermal sensitizer.

METHODS

BALB/c mice received dermal applications (vehicle or chemical) on days 1 and 7. On day 10, they received an intranasal instillation (vehicle or chemical). Whole-body plethysmography (enhanced pause) was used to monitor changes in ventilatory function and methacholine reactivity. Pulmonary inflammation was assessed by using bronchoalveolar lavage (cells, TNF-alpha levels, and macrophage inflammatory protein 2 levels). Immunologic parameters included total serum IgE levels, lymphocyte distribution in auricular and cervical lymph nodes, and IL-4 and IFN-gamma levels in supernatants of lymph node cells incubated with or without concanavalin A.

RESULTS

Mice dermally treated and intranasally challenged with TMA experienced markedly increased enhanced pause immediately after intranasal challenge and increased methacholine reactivity (24 hours later). Mice similarly treated with DNCB did not show any ventilatory changes. Neutrophil influx and increased macrophage inflammatory protein 2 and TNF-alpha levels were found in bronchoalveolar lavage fluid in both TMA- and DNCB-treated mice. The proportion of CD19+ B cells was increased in auricular and cervical lymph nodes of TMA-treated mice. IL-4 and IFN-gamma levels were increased in supernatants of concanavalin A-stimulated auricular and cervical lymph node cells of TMA- or DNCB-treated mice; however, the relative proportions of IL-4 and IFN-gamma levels differed between TMA- and DNCB-treated mice. Serum total IgE levels were increased in TMA-treated mice only.

CONCLUSION

Both compounds induce a mixed T(H)1-T(H)2 response, but only TMA induced ventilatory changes.

CLINICAL IMPLICATIONS

In the workplace avoiding skin contact with chemical sensitizers might be advised to prevent chemical-induced asthma.

摘要

背景

职业性哮喘可由化学物质引起。此前,我们使用甲苯二异氰酸酯建立了免疫介导的化学物质诱发哮喘的小鼠模型。

目的

我们试图用偏苯三酸酐(TMA,一种呼吸道致敏剂)和1-氯-2,4-二硝基苯(DNCB,一种皮肤致敏剂)验证该模型。

方法

BALB/c小鼠在第1天和第7天接受皮肤涂抹(赋形剂或化学物质)。在第10天,它们接受鼻内滴注(赋形剂或化学物质)。使用全身体积描记法(增强暂停)监测通气功能和乙酰甲胆碱反应性的变化。通过支气管肺泡灌洗(细胞、肿瘤坏死因子-α水平和巨噬细胞炎性蛋白2水平)评估肺部炎症。免疫参数包括血清总IgE水平、耳和颈淋巴结中的淋巴细胞分布,以及在有或无伴刀豆球蛋白A的情况下孵育的淋巴结细胞上清液中的白细胞介素-4和干扰素-γ水平。

结果

经TMA皮肤处理并鼻内激发的小鼠在鼻内激发后立即出现增强暂停显著增加,且乙酰甲胆碱反应性增加(24小时后)。用DNCB进行类似处理的小鼠未表现出任何通气变化。在经TMA和DNCB处理的小鼠的支气管肺泡灌洗液中均发现中性粒细胞流入以及巨噬细胞炎性蛋白2和肿瘤坏死因子-α水平增加。在经TMA处理的小鼠的耳和颈淋巴结中,CD19+B细胞的比例增加。在经TMA或DNCB处理的小鼠的伴刀豆球蛋白A刺激的耳和颈淋巴结细胞上清液中,白细胞介素-4和干扰素-γ水平增加;然而,经TMA处理和经DNCB处理的小鼠之间白细胞介素-4和干扰素-γ水平的相对比例有所不同。仅在经TMA处理的小鼠中血清总IgE水平升高。

结论

两种化合物均诱导混合的T(H)1-T(H)2反应,但只有TMA诱导通气变化。

临床意义

在工作场所,建议避免皮肤接触化学致敏剂以预防化学物质诱发的哮喘。

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