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Thymic stromal lymphopoietin: A central regulator of allergic asthma

机译:胸腺基质淋巴细胞生成素:过敏性哮喘的中枢调节剂

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Introduction: Epithelial cell-derived mediators have emerged as key players for instigating local remodeling and the associated cellular inflammation in asthmatic airways. In particular, the epithelial-derived cytokine, thymic stromal lymphopoietin (TSLP), has been identified as a master switch for allergic inflammation.Areas covered: TSLP is expressed by structural and immune cells at the site of allergen entry in the airways. Stimuli for release of TSLP include common triggers of asthma symptoms, and TSLP levels correlate with disease severity. TSLP regulates helper T cell 2 (Th2) humoral immunity through upregulating OX40L on dendritic cells (DCs), which drives Th2 lymphocytes; however, activation of several other cells by TSLP also supports the development of Th2 inflammation. Animal models of asthma demonstrate that increased levels of TSLP can induce many of the characteristics of asthma.Expert opinion: The work conducted to date supports a critical role of TSLP in the pathogenesis of allergic asthma. The first clinical trial to block the downstream effects of OX40L has shown reduced levels of circulating IgE and airway eosinophils, confirming the importance of TSLP-induced OX40L levels on DCs. Clinical trials with TSLP blockade are underway and will unequivocally confirm whether TSLP is indeed a key driver of allergic inflammation in asthma.
机译:简介:上皮细胞源性介质已成为促进哮喘气道局部重塑及相关细胞炎症的关键因素。尤其是,上皮来源的细胞因子胸腺基质淋巴细胞生成素(TSLP)已被确定为过敏性炎症的主要转换开关。覆盖的区域:TSLP由呼吸道中过敏原进入部位的结构和免疫细胞表达。释放TSLP的刺激物包括哮喘症状的常见诱因,并且TSLP水平与疾病的严重程度相关。 TSLP通过上调驱动Th2淋巴细胞的树突细胞(DC)上的OX40L来调节辅助性T细胞2(Th2)体液免疫。然而,TSLP对其他几种细胞的激活也支持Th2炎症的发展。哮喘的动物模型表明,TSLP水平升高可诱发哮喘的许多特征。专家意见:迄今为止开展的工作支持TSLP在变应性哮喘的发病机制中的关键作用。阻断OX40L下游作用的第一个临床试验显示循环IgE和气道嗜酸性粒细胞水平降低,证实了TSLP诱导的OX40L水平对DC的重要性。正在进行TSLP阻滞剂的临床试验,它将明确证实TSLP是否确实是哮喘过敏性炎症的主要驱动因素。

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