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Omalizumab: Stepping outside our comfort zone to broaden the number of those who can benefit

机译:omalizumab:踩到我们的舒适区外,扩大那些能受益的人数

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摘要

An increasing body of evidence indicates that omalizumab, a recombinant humanised IgG1 non-complement-fixing monoclonal antibody that binds to the high-affinity receptor-binding domain (Ce3) on the Fc portion of free IgE, is clinically effective in patients with intrinsic asthma [1-3], which, by definition, is asthma without atopy and, consequently, without clinical or serological evidence of IgE-mediated allergy to common environmental agents [4], and also in other morbid conditions not associated with IgE [5]. This evidence is surprising because IgE represents the substrate on which omalizumab acts. However, the possibility of also using omalizumab in non-atopic patients is extremely exciting because about one-third of adult asthmatic patients are non-atopic, and these patients usually have more severe and difficult-to-control disease [6].
机译:越来越多的证据表明omalizumab,一种重组人源化的IgG1非互补 - 固定的单克隆抗体,其与自由IgE的Fc部分的高亲和力受体结合结构域(CE3)结合,在内在哮喘的患者中临床有效 [1-3],根据定义,其哮喘没有收获,因此,没有IgE介导的常见环境代理的临床或血清学证据常见的环境代理[4],以及在与IgE无关的其他病态条件下[5] 。 这种证据令人惊讶,因为IgE表示omalizumab作用的基材。 然而,在非特应患者中使用奥马拉姆的可能性非常令人兴奋,因为约有三分之一的成年哮喘患者是非特征的,并且这些患者通常具有更严重和难以对照的疾病[6]。

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