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过敏原介导物、花生四烯酸代谢产物、血液和尿液中的嗜酸粒细胞和中性粒细胞成分导致的支气管激发试验后哮喘迟发反应。

Delayed asthmatic response to bronchial challenge with allergen-mediators, eicosanoids, eosinophil and neutrophil constituents in the blood and urine.

机构信息

Allergy Research Foundation, Breda, The Netherlands.

出版信息

Respiration. 2011;82(3):225-36. doi: 10.1159/000324542. Epub 2011 Apr 1.

DOI:10.1159/000324542
PMID:21454958
Abstract

BACKGROUND

In patients with allergic bronchial asthma, different immunologic mechanisms may participate and lead to different types of asthmatic response to allergen challenge, such as immediate/early (IAR/EAR), late (LAR) or delayed asthmatic response (DYAR).

OBJECTIVES

In 55 of 397 asthmatics, DYAR has been recorded (p < 0.001) and confirmed by repeated bronchial challenge with the same allergen (p < 0.001). DYAR began between 26 and 32 h, reached a maximum between 32 and 48 h and resolved within 56 h after the challenge. DYAR was associated with various clinical symptoms and diagnostic parameters having diverged from those recorded during the IARs/EARs and LARs.

METHODS

In 25 of 55 patients, repeated DYAR has been supplemented with the recording of leukotriene B(4) (LTB(4)), LTC(4), LTE(4), prostaglandin D(2) (PGD(2)), PGE(2), PGF(2)(α), thromboxane B(2), lipoxin A(4), eosinophil cationic protein, eosinophil-derived neurotoxin/eosinophil protein X, eosinophilic peroxidase, myeloperoxidase, histamine and tryptase in peripheral blood, and of LTC(4), thromboxane B(2), eosinophil-derived neurotoxin and 9α,11β-PGF(2) in urine, before and up to 72 h after the bronchial allergen challenge, by means of enzyme-linked immunoassay (ELISA/EIA) or ImmunoCAP.

RESULTS

DYAR was accompanied by a significant increase in the plasma concentrations of LTB(4) (p < 0.05) and myeloperoxidase (p < 0.05) at 24, 36 and 48 h after the challenge, whereas the plasma/serum or urine concentrations of the other factors did not demonstrate any significant changes (p > 0.05).

CONCLUSIONS

These results would indicate an active and prominent involvement of neutrophils, in addition to the previously demonstrated role of the Th1 lymphocytes, in the clinical DYAR.

摘要

背景

在过敏性支气管哮喘患者中,不同的免疫机制可能参与并导致对过敏原激发的不同类型的哮喘反应,如即刻/早期(IAR/EAR)、晚期(LAR)或迟发性哮喘反应(DYAR)。

目的

在 397 例哮喘患者中,记录到 55 例 DYAR(p<0.001),并通过用相同过敏原重复支气管激发得到证实(p<0.001)。DYAR 于激发后 26-32 小时开始,于 32-48 小时达到高峰,并于激发后 56 小时内缓解。DYAR 与各种临床症状和诊断参数相关,与 IARs/EARs 和 LARs 记录的参数不同。

方法

在 55 例患者中的 25 例中,重复 DYAR 并记录白细胞三烯 B4(LTB4)、LTC4、LTE4、前列腺素 D2(PGD2)、PGE2、PGF2α、血栓素 B2、脂氧素 A4、嗜酸性粒细胞阳离子蛋白、嗜酸性粒细胞衍生的神经毒素/嗜酸性粒细胞蛋白 X、嗜酸性粒细胞过氧化物酶、髓过氧化物酶、组胺和类胰蛋白酶在外周血中的浓度,以及 LTC4、血栓素 B2、嗜酸性粒细胞衍生的神经毒素和 9α,11β-PGF2 在尿液中的浓度,在支气管过敏原激发前和激发后 72 小时内,通过酶联免疫吸附测定(ELISA/EIA)或 ImmunoCAP 进行检测。

结果

DYAR 伴随着激发后 24、36 和 48 小时时血浆 LTB4(p<0.05)和髓过氧化物酶浓度的显著增加(p<0.05),而其他因素的血浆/血清或尿液浓度未显示出任何显著变化(p>0.05)。

结论

这些结果表明,除了先前证明的 Th1 淋巴细胞的作用外,中性粒细胞也积极且显著地参与了临床 DYAR。

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