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Omalizumab for severe asthma: Efficacy beyond the atopic patient?

机译:omalizumab为严重哮喘:超越特应患者的疗效?

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摘要

Several years ago, omalizumab became commercially available for the treatment of severe asthma. It remains the only monoclonal antibody to be marketed for this purpose. Since then, many studies have been published endorsing its efficacy and effectiveness. Concomitantly, evidence of an overlap between atopic and non-atopic severe asthma has emerged. However, there also appears to be some disagreement regarding the value of omalizumab in the management of non-atopic disease, as some studies have failed to show any benefit in these patients. The recent literature has also sought to identify appropriate prognostic biomarkers for the use of omalizumab, other than immunoglobulin (IgE) levels. This article briefly summarizes the evolution of asthma treatment, the pathophysiology of the condition, and the method of action of omalizumab. The author describes the controlled and uncontrolled studies (also named "real-life studies") published in adult and pediatric populations in different countries and expresses his view on the current place of the drug in the management of severe allergic asthma. He offers a personal perspective on the recent evidence for the use of omalizumab in non-atopic patients, highlighting the implications for current clinical practice and the gaps in our knowledge. The author justifies his belief that omalizumab is not only an IgE-blocking drug and should be considered as a disease-modifying therapy because of its multiple effects on different biologic pathways. Finally, some areas for future research are indicated.
机译:几年前,Omalizumab正在商业上可用于治疗严重的哮喘。它仍然是为此目的销售的唯一单克隆抗体。从那时起,许多研究已经签出了其疗效和有效性。伴随着,出现了特应性和非特性严重哮喘之间重叠的证据。然而,由于一些研究未能在这些患者中表现出任何益处,似乎似乎有关omalizumab的价值存在一些分歧。最近的文献还寻求鉴定用于使用omalizumab的适当预后生物标志物,除免疫球蛋白(IgE)水平之外。本文简要概述了哮喘治疗的演变,病情的病理生理学以及奥拉姆拉的作用方法。提交人描述了受控和不受控制的研究(也名为“现实生活研究”)在不同国家的成人和儿科人群中发表,并表达了他对药物目前的哮喘管理中的观点。他对最近在非特应患者中使用奥马拉姆的证据提供了个人视角,突出了对当前临床实践的影响和我们知识中的差距。作者证明了他的信念,即omalizumab不仅是IgE阻断的药物,并且应该被视为疾病改性治疗,因为它对不同的生物途径的多种影响。最后,指出了一些未来研究的领域。

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