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特泽泊单抗作为一种治疗重度哮喘的新兴治疗选择:现有证据。

Tezepelumab as an Emerging Therapeutic Option for the Treatment of Severe Asthma: Evidence to Date.

机构信息

Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

出版信息

Drug Des Devel Ther. 2021 Jan 27;15:331-338. doi: 10.2147/DDDT.S250825. eCollection 2021.

Abstract

Asthma is a complex heterogeneous disease defined by chronic inflammation of the airways. Patients present with wheezing, chest tightness, cough and shortness of breath. Bronchial hyperresponsiveness and variable expiratory airflow limitation are hallmark features. About 3.6-6.1% of patients, despite receiving high-dose inhaled corticosteroids (ICS) and a second controller medication, report persistent symptoms referred to as severe asthma. Uncontrolled severe asthma is associated with increased mortality, morbidity, diminished quality of life and increased health expenditures. The development of modern biological therapy has revolutionized severe asthma treatment. By targeting specific chemokines, asthma control has drastically improved, resulting in better quality of life, less emergency department visits and inpatient admissions, and decreased chronic systemic corticosteroid utilization. Despite these advances, there remains a subset of asthma patients who remain symptomatic with poor quality of life and heavy utilization of the healthcare system. Recently attention has been given to pharmaceutical therapy directed at receptors and cytokines on the epithelial layer of the lung referred to as "alarmins". Thymic stromal lymphopoietin (TSLP) is an interleukin-7-like receptor family found on the epithelial layer of the lung that releases a cytokine cascade inducing eosinophilic inflammation, mucus production and airflow obstruction in asthmatics. Tezepelumab is the first investigational monoclonal antibody that inhibits TSLP. Proof of concept study and phase IIb studies demonstrated reduced asthma exacerbations, improvement in quality of life, less decline in FEV and decrease in biochemical inflammatory markers in comparison to placebo. It is presently undergoing three phase III studies and an additional phase II study.

摘要

哮喘是一种复杂的异质性疾病,其特征为气道慢性炎症。患者表现为喘息、胸闷、咳嗽和呼吸困难。支气管高反应性和可变呼气气流受限是标志性特征。约 3.6-6.1%的患者尽管接受了高剂量吸入皮质类固醇(ICS)和第二种控制药物治疗,但仍存在持续症状,称为严重哮喘。未得到控制的严重哮喘与死亡率增加、发病率增加、生活质量下降和医疗费用增加有关。现代生物疗法的发展彻底改变了严重哮喘的治疗方法。通过靶向特定趋化因子,哮喘控制得到了极大改善,从而提高了生活质量,减少了急诊就诊和住院治疗,降低了慢性全身性皮质类固醇的使用。尽管取得了这些进展,但仍有一部分哮喘患者存在症状,生活质量差,对医疗系统的利用度高。最近,人们关注了针对肺部上皮细胞层上的受体和细胞因子的药物治疗,这些受体和细胞因子被称为“警报素”。胸腺基质淋巴细胞生成素(TSLP)是一种白细胞介素-7 样受体家族,存在于肺部的上皮细胞层,释放细胞因子级联反应,诱导哮喘患者中的嗜酸性粒细胞炎症、黏液产生和气流阻塞。Tezepelumab 是一种研究中的抑制 TSLP 的单克隆抗体。概念验证研究和 IIb 期研究表明,与安慰剂相比,该药可减少哮喘加重、改善生活质量、减少 FEV 下降和降低生化炎症标志物。目前正在进行三项 III 期研究和一项额外的 II 期研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d09/7850420/3ec9e5d4d53f/DDDT-15-331-g0001.jpg

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