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调节性T细胞在严重马哮喘小鼠模型中的调节作用。

Modulatory role of regulatory T cells in a murine model of severe equine asthma.

作者信息

Henríquez Claudio, Morán Gabriel, Carrasco Cristian, Sarmiento José, Barría Miguel, Folch Hugo, Uberti Benjamin

机构信息

Pharmacology and Morphophysiology Department, Faculty of Veterinary Sciences, Universidad Austral de Chile, Valdivia, Chile.

Pathology Department, Regional Hospital of Valdivia, Valdivia, Chile.

出版信息

BMC Vet Res. 2017 Apr 28;13(1):117. doi: 10.1186/s12917-017-1037-0.

Abstract

BACKGROUND

It is accepted that T regulatory cells (Treg) control different types of immune responses. In connection with this role, we have recently described an important increase in CD4+, CD25, Foxp3+ lymphocytes in the airway system of horses coursing with an exacerbation of severe equine asthma (EA). To explore the potential role of this population in the resolution of EA inflammation, we used a murine experimental model in which airway neutrophilic inflammation, which is similar to that observed in EA, is induced in mice by continual exposure to Aspergillus fumigatus contaminated hay. This model has the advantage that in mice we may induce a reduction of the Treg population using low doses of cyclophosphamide (Cy).

RESULTS

The results indicated that the percentage of Treg cells increased with allergen exposure, as in horses; and animals partially depleted of Treg cells by treatment with Cy showed increased airway inflammation, demonstrated by an increased percentage of neutrophils and specific immunoglobulins in bronchoalveolar lavage fluid (BALF). Furthermore, a histopathologic study of animals that were pretreated with Cy before antigenic challenge showed higher cellular infiltration in the lung and deeper remodeling changes in the bronchi, including epithelial and goblet cell hyperplasia as well as airway smooth muscle hypertrophy.

CONCLUSION

In this murine model of EA, the reduced number and function of Treg induced by low doses of Cy, which directly correlates with increased airway inflammation and lung infiltration, indicates that Treg may play a major role in the regulation and resolution of EA.

摘要

背景

调节性T细胞(Treg)可控制不同类型的免疫反应,这一点已得到公认。鉴于此作用,我们最近发现,患有严重马哮喘(EA)急性加重期的马匹气道系统中CD4 +、CD25、Foxp3 +淋巴细胞显著增加。为探究该细胞群在EA炎症消退中的潜在作用,我们使用了一种小鼠实验模型,通过持续暴露于被烟曲霉污染的干草,在小鼠中诱导出与EA中观察到的类似的气道嗜中性粒细胞炎症。该模型的优势在于,我们可以使用低剂量环磷酰胺(Cy)在小鼠中诱导Treg细胞数量减少。

结果

结果表明,与马匹一样,Treg细胞百分比随变应原暴露而增加;用Cy处理使Treg细胞部分耗竭的动物,气道炎症增加,支气管肺泡灌洗液(BALF)中嗜中性粒细胞百分比和特异性免疫球蛋白增加证明了这一点。此外,对抗抗原攻击前用Cy预处理的动物进行组织病理学研究发现,肺中细胞浸润更多,支气管重塑变化更深,包括上皮细胞和杯状细胞增生以及气道平滑肌肥大。

结论

在该EA小鼠模型中,低剂量Cy诱导的Treg数量和功能减少与气道炎症增加和肺浸润直接相关,表明Treg可能在EA的调节和消退中起主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f65d/5410054/f2cf96a33dc5/12917_2017_1037_Fig1_HTML.jpg

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