首页> 外文期刊>The Journal of Experomental Medicine >Induction of Airway Mucus Production By T Helper 2 (Th2) Cells: A Critical Role For Interleukin 4 In Cell Recruitment But Not Mucus Production
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Induction of Airway Mucus Production By T Helper 2 (Th2) Cells: A Critical Role For Interleukin 4 In Cell Recruitment But Not Mucus Production

机译:T辅助细胞2(Th2)诱导气道粘液产生:白细胞介素4在细胞募集而不是粘液产生中的关键作用

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摘要

Airway inflammation is believed to stimulate mucus production in asthmatic patients. Increased mucus secretion is an important clinical symptom and contributes to airway obstruction in asthma. Activated CD4 Th1 and Th2 cells have both been identified in airway biopsies of asthmatics but their role in mucus production is not clear. Using CD4 T cells from mice transgenic for the OVA-specific TCR, we studied the role of Th1 and Th2 cells in airway inflammation and mucus production. Airway inflammation induced by Th2 cells was comprised of eosinophils and lymphocytes; features found in asthmatic patients. Additionally, there was a marked increase in mucus production in mice that received Th2 cells and inhaled OVA, but not in mice that received Th1 cells. However, OVA-specific Th2 cells from IL-4–deficient mice were not recruited to the lung and did not induce mucus production. When this defect in homing was overcome by administration of TNF-α, IL-4 ?/? Th2 cells induced mucus as effectively as IL-4 +/+ Th2 cells. These studies establish a role for Th2 cells in mucus production and dissect the effector functions of IL-4 in these processes. These data suggest that IL-4 is crucial for Th2 cell recruitment to the lung and for induction of inflammation, but has no direct role in mucus production.
机译:据信气道炎症刺激哮喘患者中的粘液产生。粘液分泌增加是重要的临床症状,并导致哮喘的气道阻塞。哮喘患者的气道活检中均已鉴定出活化的CD4 Th1和Th2细胞,但尚不清楚它们在粘液产生中的作用。使用来自转基因小鼠的OVA特异性TCR的CD4 T细胞,我们研究了Th1和Th2细胞在气道炎症和粘液产生中的作用。 Th2细胞诱导的气道炎症包括嗜酸性粒细胞和淋巴细胞。在哮喘患者中发现的特征。此外,在接受Th2细胞和吸入OVA的小鼠中,粘液产生显着增加,但在接受Th1细胞的小鼠中则没有。但是,来自IL-4缺陷型小鼠的OVA特异性Th2细胞并未募集到肺部,也没有诱导粘液产生。当通过施用TNF-α克服了归巢中的缺陷时,IL-4α/β就可以了。 Th2细胞与IL-4 + / + Th2细胞一样有效地诱导粘液。这些研究确立了Th2细胞在粘液产生中的作用,并在这些过程中剖析了IL-4的效应子功能。这些数据表明,IL-4对于Th2细胞募集至肺部和诱导炎症至关重要,但在粘液产生中没有直接作用。

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