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DESTINATION: a phase 3 multicentre randomized double-blind placebo-controlled parallel-group trial to evaluate the long-term safety and tolerability of tezepelumab in adults and adolescents with severe uncontrolled asthma

机译:目的地:第3阶段多期随机双盲安慰剂控制并联试验以评估Tezepelumab在成人和青少年中具有严重不受控制的哮喘的长期安全性和耐受性

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摘要

Mechanism of action by which tezepelumab improves clinical outcomes in patients with severe asthma. TSLP is released from the airway epithelium in response to insults such as viruses, allergens and pollutants, triggering multiple inflammatory cascades. Tezepelumab specifically blocks TSLP from binding to its heterodimeric receptor, thereby inhibiting the production of various inflammatory cytokines and cell types. Treatment with tezepelumab has thus far been shown to reduce blood eosinophil count, IgE, IL-5, IL-13 and FeNO. FeNO fractional exhaled nitric oxide, IgE immunoglobulin E, IL interleukin, ILC2 type 2 innate lymphoid cell, Th T‑helper, TSLP thymic stromal lymphopoietin
机译:Tezepelumab改善严重哮喘患者的临床结果的作用机制。 TSLP从气道上皮释放,响应诸如病毒,过敏原和污染物等损伤,引发多种炎症级联。 Tezepelumab特异性地阻断TSLP与其异二聚体受体的结合,从而抑制各种炎性细胞因子和细胞类型的产生。迄今已迄今对Tezepelumab进行治疗可降低血液嗜纤度计数,IgE,IL-5,IL-13和FENO。 Feno分数呼出一氧化氮,IgE免疫球蛋白E,IL白细胞介素,ILC2 2型先天淋巴细胞,TH T-Helper,TSLP胸腺基质淋巴泛素

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