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儿科哮喘中单克隆抗体治疗的前景。

Prospects for Monoclonal Antibody Therapy in Pediatric Asthma.

机构信息

Rutgers New Jersey Medical School, The State University of New Jersey, 90 Bergen Street, Newark, NJ, 07103, USA.

出版信息

Curr Allergy Asthma Rep. 2018 Jul 10;18(9):45. doi: 10.1007/s11882-018-0799-1.

DOI:10.1007/s11882-018-0799-1
PMID:29992472
Abstract

PURPOSE OF REVIEW

The profile of biologic therapies for asthma is growing rapidly. We discuss how to match the proper pediatric patient with the most effective therapy.

RECENT FINDINGS

Currently available biologic therapies are most effective in patients with T2 high asthma. Newer drugs are currently being studied which target TSLP and interleukin 33. These newer drugs may provide options for asthmatics who do not respond to the current anti-IgE, anti-IL5, and anti-IL4/13 therapies. Asthma is a heterogeneous disease which can be driven by different inflammatory mediators in different patients. To select the most effective biologic therapy for a pediatric patient, the asthma phenotype must first be determined. The steep cost of biologics limits their use, which makes proper pairing of patient to therapy even more crucial. Presently, several therapies exist for T2 high asthma, but it is hoped in the future that development of drugs effective for T2 low asthmatics will be available as well.

摘要

目的综述

哮喘的生物疗法种类迅速增加。我们讨论如何将合适的儿科患者与最有效的治疗方法相匹配。

最近的发现

目前可用的生物疗法在 T2 高型哮喘患者中最有效。目前正在研究靶向 TSLP 和白细胞介素 33 的新型药物。对于那些对当前的抗 IgE、抗 IL5 和抗 IL4/13 治疗没有反应的哮喘患者,这些新型药物可能提供了选择。哮喘是一种异质性疾病,在不同患者中可能由不同的炎症介质驱动。为了为儿科患者选择最有效的生物治疗方法,首先必须确定哮喘表型。生物制剂的高昂成本限制了它们的使用,这使得患者与治疗方法的正确配对更加关键。目前,针对 T2 高型哮喘有几种治疗方法,但希望未来也能开发出针对 T2 低型哮喘有效的药物。

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本文引用的文献

1
Tralokinumab for severe, uncontrolled asthma (STRATOS 1 and STRATOS 2): two randomised, double-blind, placebo-controlled, phase 3 clinical trials.特利鲁单抗治疗重症、未控制哮喘(STRATOS 1 和 STRATOS 2):两项随机、双盲、安慰剂对照、3 期临床试验。
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Efficacy and Safety of Dupilumab in Glucocorticoid-Dependent Severe Asthma.度普利尤单抗治疗糖皮质激素依赖型重症哮喘的疗效和安全性。
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度普利尤单抗在中重度未控制哮喘中的疗效和安全性。
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Small Molecule Mimetics of α-Helical Domain of IRAK2 Attenuate the Proinflammatory Effects of IL-33 in Asthma-like Mouse Models.小分子 IRAK2 螺旋区模拟物可减轻哮喘样小鼠模型中 IL-33 的促炎作用。
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IL-33 and Its Receptor ST2 after Inhaled Allergen Challenge in Allergic Asthmatics.过敏性哮喘患者吸入变应原后白细胞介素 33 及其受体 ST2 的变化
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Guiding principles for use of newer biologics and bronchial thermoplasty for patients with severe asthma.重度哮喘患者使用新型生物制剂和支气管热成形术的指导原则。
Ann Allergy Asthma Immunol. 2017 Dec;119(6):533-540. doi: 10.1016/j.anai.2017.09.058. Epub 2017 Nov 2.
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Tezepelumab in Adults with Uncontrolled Asthma.特泽布尔单抗在未控制的哮喘成人中的应用。
N Engl J Med. 2017 Sep 7;377(10):936-946. doi: 10.1056/NEJMoa1704064.
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The association between blood eosinophil count and benralizumab efficacy for patients with severe, uncontrolled asthma: subanalyses of the Phase III SIROCCO and CALIMA studies.严重未控制哮喘患者血液嗜酸性粒细胞计数与贝那利珠单抗疗效之间的关联:III期SIROCCO和CALIMA研究的亚组分析
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