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γ-Secretase Inhibitor Alleviates Acute Airway Inflammation of Allergic Asthma in Mice by Downregulating Th17 Cell Differentiation

机译:γ-秘密酶抑制剂可通过下调Th17细胞分化来减轻小鼠过敏性哮喘的急性气道炎症

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摘要

T helper 17 (Th17) cells play an important role in the pathogenesis of allergic asthma. Th17 cell differentiation requires Notch signaling. γ-Secretase inhibitor (GSI) blocks Notch signaling; thus, it may be considered as a potential treatment for allergic asthma. The aim of this study was to evaluate the effect of GSI on Th17 cell differentiation in a mouse model of allergic asthma. OVA was used to induce mouse asthma model in the presence and absence of GSI. GSI ameliorated the development of OVA-induced asthma, including suppressing airway inflammation responses and reducing the severity of clinical signs. GSI also significantly suppressed Th17-cell responses in spleen and reduced IL-17 levels in serum. These findings suggest that GSI directly regulates Th17 responses through a Notch signaling-dependent pathway in mouse model of allergic asthma, supporting the notion that GSI is a potential therapeutic agent for the treatment of allergic asthma.
机译:T辅助细胞17(Th17)细胞在过敏性哮喘的发病机理中起重要作用。 Th17细胞分化需要Notch信号传导。 γ-分泌酶抑制剂(GSI)阻断Notch信号传导;因此,它可能被认为是过敏性哮喘的潜在治疗方法。这项研究的目的是评估变应性哮喘小鼠模型中GSI对Th17细胞分化的影响。在存在和不存在GSI的情况下,OVA均可用于诱导小鼠哮喘模型。 GSI改善了OVA诱发的哮喘的发展,包括抑制气道炎症反应并降低临床症状的严重性。 GSI还显着抑制脾脏中的Th17细胞反应,并降低血清中的IL-17水平。这些发现表明,GSI通过Notch信号依赖型途径在过敏性哮喘小鼠模型中直接调节Th17应答,支持了GSI是潜在的治疗过敏性哮喘的治疗剂的观点。

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