New Drug for Management of Severe Uncontrolled Asthma: Tezepelumab

Manvi Sharma, Prince P. George, Ranjeet Kumar, Amit Sharma
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Abstract

Tezepelumab is a first-in-class human IgG2λ monoclonal antibody used to treat severe, uncontrolled asthma. Tezepelumab acts by hindering the action of thymic stromal lymphopoietin (TSLP), an epithelial-derived cytokine that triggers an immunological response by binding to TSLP and thereby preventing its binding with the TSLP receptor complex. TSLP has a critical role in Th2 immunity and plays an important role in the pathogenesis of asthma because it stimulates the production of Th2-associated inflammatory mediators, such as interleukin-4, interleukin-5, interleukin-9, and interleukin-13. It is the first biologic with no phenotypic or biomarker restrictions that has been approved for use in severe asthma. Tezepelumab is indicated in severe, uncontrolled asthma patients due to its safety, tolerability, and efficacy. Adults with severe, uncontrolled asthma experienced considerably lower annualised asthma exacerbation rates (AAERs) when administered with tezepelumab compared to a placebo. These preliminary results indicated that the TSLP-induced release of T2 inflammatory mediators may be reduced, and the sustained inhibition was maintained over a 52-week treatment period. In this review, we have summarised various phase III clinical trials and the mechanism of action of tezepelumab in severe, uncontrolled asthma.
治疗严重失控哮喘的新药:特珠单抗
Tezepelumab 是一种首创的人类 IgG2λ 单克隆抗体,用于治疗严重的、无法控制的哮喘。TSLP是一种上皮源性细胞因子,通过与TSLP结合并阻止其与TSLP受体复合物结合而触发免疫反应。TSLP 在 Th2 免疫中起着关键作用,并在哮喘发病机制中起着重要作用,因为它能刺激 Th2 相关炎症介质的产生,如白细胞介素-4、白细胞介素-5、白细胞介素-9 和白细胞介素-13。它是第一个没有表型或生物标志物限制的生物制剂,已被批准用于重症哮喘。特珠单抗因其安全性、耐受性和有效性而适用于严重的、未得到控制的哮喘患者。与安慰剂相比,患有严重、未得到控制的哮喘的成人在使用替塞单抗后,哮喘的年恶化率(AAER)大大降低。这些初步结果表明,TSLP诱导的T2炎症介质释放可能会减少,而且持续的抑制作用在52周的治疗期内得以维持。在这篇综述中,我们总结了各种 III 期临床试验和替塞普鲁单抗在严重、失控哮喘中的作用机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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