Huston David P, Liu Yong Jun
Immunology Allergy & Rheumatology Section,Baylor College of Medicine, One Baylor Plaza,BCM 285, Houston TX 77030, USA.
Curr Allergy Asthma Rep. 2006 Sep;6(5):372-6. doi: 10.1007/s11882-996-0006-7.
Thymic stromal lymphopoietin (TSLP) is an interleukin (IL)-7-like cytokine that has recently been implicated as central to the microenvironment and is permissive for the immunologic cascade that initiates and propagates allergic immune responses. In humans, TSLP is produced predominantly by epithelial cells and activated mast cells, and stimulates myeloid dendritic cells (mDC), which uniquely express the heterodimeric TSLP receptor. TSLP-activated mDC can promote naïve CD4+ T cells to differentiate into a Th2 phenotype and can promote the expansion of CD4+ Th2 memory cells. Recent evidence implicates TSLP as playing a pivotal role in the pathobiology of allergic asthma and atopic dermatitis. The potential for TSLP to provide a new therapeutic target for the treatment of allergic disorders is compelling, and elucidating the mechanisms that regulate TSLP expression and the effects of TSLP on orchestrating the immune response toward a Th2 phenotype should facilitate this quest.
胸腺基质淋巴细胞生成素(TSLP)是一种白细胞介素(IL)-7样细胞因子,最近被认为是微环境的核心要素,对启动和传播过敏性免疫反应的免疫级联反应具有促进作用。在人类中,TSLP主要由上皮细胞和活化的肥大细胞产生,并刺激独特表达异二聚体TSLP受体的髓样树突状细胞(mDC)。TSLP激活的mDC可促进初始CD4+ T细胞分化为Th2表型,并可促进CD4+ Th2记忆细胞的扩增。最近的证据表明TSLP在过敏性哮喘和特应性皮炎的病理生物学中起关键作用。TSLP为过敏性疾病治疗提供新治疗靶点的潜力令人信服,阐明调节TSLP表达的机制以及TSLP对协调针对Th2表型的免疫反应的影响应有助于实现这一目标。