Omalizumab in the Therapy of Pediatric Asthma.

IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Recent patents on inflammation & allergy drug discovery Pub Date : 2018-01-01 DOI:10.2174/1872213X12666180430161351
Dimitri Poddighe, Ilaria Brambilla, Amelia Licari, Gian L Marseglia
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引用次数: 17

Abstract

Background: Eosinophilic asthma is driven by Th2 immune response and is usually characterized by the increase of total serum IgE levels and/or specific IgE that express single or multiple allergen sensitization. In such an immuno-pathological background, the anti-IgE therapy, namely omalizumab, found its main clinical utility and recommendation to treat severe asthma.

Objective: In this mini-review, we summarized the most relevant immuno-pathological and clinical evidences supporting the use of omalizumab in the therapy of pediatric asthma. Furthermore, we provided the main practical points for its use in the therapeutic management of asthmatic children.

Method: Through the binding of serum free IgE, omalizumab impairs not only the effector phase of IgE-mediated asthma, but also affects the IgE biology and the related immune response, globally. Here, the history of omalizaumab has been shortly reviewed from its preclinical development to its clinical validation in pediatric asthma. Thus, recent patents regarding anti-IgE therapy have been discussed.

Conclusion: Omalizumab significantly improved the clinical management of severe and uncontrolled pediatric asthma; however, pre-treament IgE levels limited the use of omalizumab in some patients and the cost of the therapy is still relevant. Moreover, the optimal duration of the treatment with omalizumab in children has to be determined. Finally, the recent generation of a mutant IgE-Fc fragment being resistant to omalizumab binding might open further therapeutic applications, in addition to second generation anti-IgE antibodies.

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Omalizumab治疗儿童哮喘。
背景:嗜酸性哮喘是由Th2免疫反应驱动的,通常以血清总IgE水平和/或表达单一或多种过敏原致敏的特异性IgE升高为特征。在这样的免疫病理背景下,抗ige治疗,即omalizumab,发现了其主要的临床应用和推荐治疗严重哮喘。目的:在这篇小型综述中,我们总结了支持使用omalizumab治疗儿童哮喘的最相关的免疫病理和临床证据。此外,我们还提供了其在哮喘儿童治疗管理中的主要实用要点。方法:omalizumab通过与血清游离IgE的结合,不仅损害IgE介导哮喘的效应期,而且从整体上影响IgE生物学及相关免疫反应。本文简要回顾了omalizaumab从临床前开发到儿科哮喘临床验证的历史。因此,最近的专利有关抗ige治疗进行了讨论。结论:Omalizumab显著改善了重症和未控制的儿童哮喘的临床管理;然而,治疗前的IgE水平限制了omalizumab在一些患者中的使用,并且治疗的成本仍然相关。此外,儿童用omalizumab治疗的最佳持续时间必须确定。最后,除了第二代抗ige抗体外,最近一代对omalizumab结合具有抗性的突变IgE-Fc片段可能会开辟进一步的治疗应用。
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来源期刊
CiteScore
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期刊介绍: Recent Patents on Inflammation & Allergy Drug Discovery publishes review articles by experts on recent patents in the field of inflammation and allergy drug discovery e.g. on novel bioactive compounds, analogs and targets. A selection of important and recent patents in the field is also included in the journal. The journal is essential reading for all researchers involved in inflammation and allergy drug design and discovery.
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