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卵清蛋白吸入后气道炎症的消退:ISS DNA与皮质类固醇的比较

Resolution of airway inflammation following ovalbumin inhalation: comparison of ISS DNA and corticosteroids.

作者信息

Ikeda Reid K, Nayar Jyothi, Cho Jae Youn, Miller Marina, Rodriguez Monica, Raz Eyal, Broide David H

机构信息

Department of Medicine, University of California-San Diego, La Jolla, CA 92093-0635, USA.

出版信息

Am J Respir Cell Mol Biol. 2003 Jun;28(6):655-63. doi: 10.1165/rcmb.4853.

Abstract

In this study we have compared the therapeutic effect of the administration of immunostimulatory DNA sequences (ISS) with that of corticosteroids on the resolution of airway inflammation and airway hyperreactivity (AHR) in a mouse model. Mice which had already developed significant levels of eosinophilic airway inflammation 24 h after allergen challenge were then treated with either ISS or corticosteroids, and the effect on AHR and airway inflammation assessed 6 d later. ISS inhibited AHR as effectively as corticosteroids. Combination therapy with ISS and corticosteroids was more effective than monotherapy with either ISS or corticosteroids in inhibiting AHR. In ovalbumin-challenged mice, levels of bronchoalveolar lavage (BAL) eosinophils were significantly reduced with either ISS or corticosteroids. ISS induced significant levels of BAL interferon-gamma, whereas corticosteroids did not induce expression of BAL interferon-gamma. Both ISS and corticosteroids significantly reduced levels of interleukin-5 in BAL, as well as the number of Periodic Acid Schiff-positive airway epithelial cells. Corticosteroids, but not ISS, increased the number of eosinophils in regional mediastinal lymph nodes. Very few apoptotic peribronchial cells were noted following ovalbumin challenge as assessed by TUNEL assay. Corticosteroids, but not ISS, induced an increase in the small number of apoptotic peribronchial cells. The mechanism by which either ISS or corticosteroids inhibit AHR is likely to be mediated by distinct and shared cellular pathways. The combination of the shared and distinct anti-inflammatory pathways may account for the additive effect of ISS and corticosteroids on inhibiting AHR.

摘要

在本研究中,我们比较了免疫刺激DNA序列(ISS)与皮质类固醇对小鼠模型气道炎症消退和气道高反应性(AHR)的治疗效果。在变应原激发24小时后已出现显著嗜酸性气道炎症水平的小鼠,随后用ISS或皮质类固醇进行治疗,并在6天后评估对AHR和气道炎症的影响。ISS抑制AHR的效果与皮质类固醇一样有效。ISS与皮质类固醇联合治疗在抑制AHR方面比单独使用ISS或皮质类固醇单药治疗更有效。在卵清蛋白激发的小鼠中,ISS或皮质类固醇均可显著降低支气管肺泡灌洗(BAL)嗜酸性粒细胞水平。ISS可诱导显著水平的BAL干扰素-γ,而皮质类固醇不会诱导BAL干扰素-γ的表达。ISS和皮质类固醇均可显著降低BAL中白细胞介素-5的水平以及过碘酸希夫染色阳性气道上皮细胞的数量。皮质类固醇而非ISS可增加区域纵隔淋巴结中嗜酸性粒细胞的数量。通过TUNEL分析评估,卵清蛋白激发后很少观察到凋亡的支气管周围细胞。皮质类固醇而非ISS可诱导少量凋亡支气管周围细胞数量增加。ISS或皮质类固醇抑制AHR的机制可能由不同且共同的细胞途径介导。共同和不同抗炎途径的组合可能解释了ISS和皮质类固醇在抑制AHR方面的相加作用。

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