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抗IgE人源化单克隆抗体在豚草诱发的变应性鼻炎中的应用。

Use of an anti-IgE humanized monoclonal antibody in ragweed-induced allergic rhinitis.

作者信息

Casale T B, Bernstein I L, Busse W W, LaForce C F, Tinkelman D G, Stoltz R R, Dockhorn R J, Reimann J, Su J Q, Fick R B, Adelman D C

机构信息

Department of Internal Medicine, University of Iowa, Iowa City, USA.

出版信息

J Allergy Clin Immunol. 1997 Jul;100(1):110-21. doi: 10.1016/s0091-6749(97)70202-1.

Abstract

BACKGROUND

Increased serum levels of antigen-specific IgE are often associated with allergic respiratory disorders. RhuMAb-E25, a recombinant humanized monoclonal antibody, decreases free serum IgE by forming biologically inactive immune complexes with free IgE.

OBJECTIVE

We hypothesized that rhuMAb-E25 would decrease total serum IgE and reduce symptoms.

METHODS

Two hundred forty subjects were enrolled into five groups to determine the safety, tolerance, and efficacy of repeated administration of rhuMAb-E25 in adults with ragweed-induced allergic rhinitis and to explore the pharmacodynamic relationship of rhuMAb-E25 and IgE. One hundred eighty-one subjects received an initial intravenous loading dose (day 0, 1 month before ragweed season), followed by administration of rhuMAb-E25 (in mg/kg body weight) of 0.15 mg/kg subcutaneously, 0.15 mg/kg intravenously, or 0.5 mg/kg intravenously on days 7, 14, 28, 42, 56, 70, and 84. A subcutaneous placebo group and an intravenous placebo group were included. The total evaluation time included the 84-day treatment period, followed by a 42-day observation period.

RESULTS

Adverse events were mild, and no differences were observed in the rates between the three active and two placebo treatment groups. Ragweed-specific IgE levels correlated with symptom scores. RhuMAb-E25 decreased serum free IgE levels in a dose- and baseline IgE-dependent fashion. However, only 11 subjects had IgE levels that were suppressed to undetectable levels (< or = 24 ng/ml), a sample too small to demonstrate significant differences and clinical efficacy. Thus the case for efficacy was not proven. Nonetheless, the study confirms that it is safe to repeatedly administer rhuMAb-E25 over a period of months.

CONCLUSIONS

Because rhuMAb-E25 decreased serum free IgE in a dose-dependent fashion and because symptom scores correlated with antigen-specific IgE levels, the results suggest that if given in adequate doses, rhuMAb-E25 should be an effective therapy for allergic diseases.

摘要

背景

血清中抗原特异性IgE水平升高常与过敏性呼吸道疾病相关。重组人源化单克隆抗体RhuMAb-E25通过与游离IgE形成无生物活性的免疫复合物来降低血清游离IgE水平。

目的

我们假设RhuMAb-E25会降低血清总IgE水平并减轻症状。

方法

240名受试者被分为五组,以确定重复给予RhuMAb-E25对豚草诱发的成人过敏性鼻炎的安全性、耐受性和疗效,并探讨RhuMAb-E25与IgE之间的药效关系。181名受试者在第0天(豚草季节前1个月)接受初始静脉负荷剂量,随后在第7、14、28、42、56、70和84天分别皮下注射0.15 mg/kg、静脉注射0.15 mg/kg或静脉注射0.5 mg/kg的RhuMAb-E25(按体重mg/kg计算)。设立皮下安慰剂组和静脉安慰剂组。总评估时间包括84天的治疗期,随后是42天的观察期。

结果

不良事件较轻,三个活性治疗组和两个安慰剂治疗组之间的发生率无差异。豚草特异性IgE水平与症状评分相关。RhuMAb-E25以剂量和基线IgE依赖的方式降低血清游离IgE水平。然而,只有11名受试者的IgE水平被抑制到无法检测的水平(≤24 ng/ml),样本量太小,无法显示出显著差异和临床疗效。因此,疗效未得到证实。尽管如此,该研究证实了在数月内重复给予RhuMAb-E25是安全的。

结论

由于RhuMAb-E25以剂量依赖的方式降低血清游离IgE水平,且症状评分与抗原特异性IgE水平相关,结果表明,如果给予足够剂量,RhuMAb-E25应该是治疗过敏性疾病的有效疗法。

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