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Human plasma-derived C1 esterase inhibitor concentrate has limited effect on house dust mite-induced allergic lung inflammation in mice

机译:人血浆来源的C1酯酶抑制剂浓缩物对小鼠尘螨诱发的过敏性肺部炎症的作用有限

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摘要

C1 esterase inhibitor (C1-INH) can inhibit multiple pathways (complement, contact-kinin, coagulation, and fibrinolysis) that are all implicated in the pathophysiology of asthma. We explored the effect of human plasma-derived C1-INH on allergic lung inflammation in a house dust mite (HDM) induced asthma mouse model by daily administration of C1-INH (15 U) during the challenge phase. NaCl and HDM exposed mice had comparable plasma C1-INH levels, while bronchoalveolar lavage fluid (BALF) levels were increased in HDM exposed mice coinciding with slightly reduced activation of complement (C5a). C1-INH treatment reduced Th2 response and enhanced HDM-specific IgG1. Influx of eosinophils in BALF or lung, pulmonary damage, mucus production, procoagulant response or plasma leakage in BALF was similar in both groups. In conclusion, C1-INH dampens Th2 responses during HDM induced allergic lung inflammation.
机译:C1酯酶抑制剂(C1-INH)可以抑制多种途径(补体,接触激肽,凝血和纤维蛋白溶解),这些途径均与哮喘的病理生理有关。我们通过在挑战阶段每天施用C1-INH(15 U),探索了人类血浆来源的C1-INH对室内尘螨(HDM)诱发的哮喘小鼠模型中变应性肺部炎症的影响。暴露于NaCl和HDM的小鼠血浆C1-INH水平相当,而暴露于HDM的小鼠中支气管肺泡灌洗液(BALF)水平升高,这与补体(C5a)活化程度略有降低相吻合。 C1-INH处理可降低Th2反应并增强HDM特异性IgG1。两组中BALF或肺中嗜酸性粒细胞的流入,肺损伤,粘液产生,促凝反应或血浆渗漏相似。总之,C1-INH抑制了HDM引起的过敏性肺部炎症期间的Th2反应。

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