Walker S, Monteil M, Phelan K, Lasserson T J, Walters E H
National Respiratory Training Centre, The Athenaeum, 10 Church Street, Warwick, UK, CV34 4AB.
Cochrane Database Syst Rev. 2003(3):CD003559. doi: 10.1002/14651858.CD003559.
Omalizumab is a recombinant humanised monoclonal antibody directed against immunoglobulin E (IgE) to inhibit the immune system's response to allergen exposure. Omalizumab is directed against the binding site of IgE for its high affinity Fc receptor. It prevents free serum IgE from attaching to mast cells and other effector cells and prevents IgE mediated inflammatory changes. The complexes of Omalizumab and IgE formed as a result of treatment are small and not thought to be able to trigger complement activation or give rise to immune complex mediated pathology.
To determine the efficacy of anti-IgE in patients with allergic asthma.
We searched the Cochrane Airways Group Asthma trials register (February 2003) for potentially relevant studies.
Randomised control trials examining anti-IgE administered in any manner for any duration.
Two reviewers independently assessed study quality and extracted and entered data. Three modes of administration were identified from the published literature (inhaled, intravenous and subcutaneous injection). Subgroup analysis was performed by asthma severity. Data were extracted from published and unpublished sources.
Eight trials were included in the review, contributing a total of 2037 mild to severe allergic asthmatic participants with high levels of IgE. Treatment with intravenous and subcutaneous Omalizumab resulted in a 98 to 99% reduction in free IgE, reductions which were not observed following placebo treatment. Significant increases in the number of participants who were able to reduce (> 50% reduction in daily corticosteroid usage (four trials): odds ratio (OR) 2.50, 95% confidence interval (CI) 2.02 to 3.10; or completely withdraw their daily steroid intake (four trials): OR 2.50, 95%CI 2.00 to 3.13, were observed. Participants treated with Omalizumab were less likely to suffer an asthma exacerbation (stable steroid phase (three trials): OR 0.46, 95%CI 0.35 to 0.61; steroid reduction phase (three trials) OR 0.46, 95% CI 0.36 to 0.59).
REVIEWER'S CONCLUSIONS: Omalizumab was significantly more effective than placebo at increasing the numbers of patients who were able to reduce or withdraw their inhaled steroids and was effective in reducing asthma exacerbations. Omalizumab was well tolerated, although the safety profile requires longer term assessment. Patient and physician assessment of the drug was positive. Further assessment in paediatric and severe adult populations is necessary, as is comparison with inhaled corticosteroids.
奥马珠单抗是一种重组人源化单克隆抗体,可靶向免疫球蛋白E(IgE),以抑制免疫系统对过敏原暴露的反应。奥马珠单抗针对IgE与高亲和力Fc受体的结合位点。它可防止游离血清IgE附着于肥大细胞和其他效应细胞,并防止IgE介导的炎症变化。治疗后形成的奥马珠单抗与IgE复合物体积较小,一般认为不会引发补体激活或导致免疫复合物介导的病理改变。
确定抗IgE治疗对过敏性哮喘患者的疗效。
我们检索了Cochrane气道组哮喘试验注册库(2003年2月),以查找潜在的相关研究。
以任何方式、在任何时间段给予抗IgE治疗的随机对照试验。
两名评价员独立评估研究质量,并提取和录入数据。从已发表的文献中确定了三种给药方式(吸入、静脉注射和皮下注射)。按哮喘严重程度进行亚组分析。数据从已发表和未发表的资料中提取。
本综述纳入了8项试验,共纳入2037例轻至重度过敏性哮喘且IgE水平较高的患者。静脉注射和皮下注射奥马珠单抗治疗可使游离IgE降低98%至99%,而安慰剂治疗未观察到这种降低。能够减少每日皮质类固醇用量(>50%减少,4项试验)的参与者数量显著增加:比值比(OR)为2.50,95%置信区间(CI)为2.02至3.10;或完全停用每日类固醇摄入量(4项试验):OR为2.50,95%CI为2.00至3.13。接受奥马珠单抗治疗的参与者哮喘发作的可能性较小(稳定类固醇阶段,3项试验:OR为0.46,95%CI为0.35至0.61;类固醇减量阶段,3项试验:OR为0.46,95%CI为