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
Department of Internal Medicine, University of Iowa, Iowa City, USA.
J Allergy Clin Immunol. 1997 Jul;100(1):110-21. doi: 10.1016/s0091-6749(97)70202-1.
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.
We hypothesized that rhuMAb-E25 would decrease total serum IgE and reduce symptoms.
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.
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.
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.
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。
我们假设RhuMAb-E25会降低血清总IgE水平并减轻症状。
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。
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。
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。