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遗传性血管性水肿患者重组人 C1 抑制剂的免疫安全性:ige 抗体评估。

Immunosafety of recombinant human C1-inhibitor in hereditary angioedema: evaluation of ige antibodies.

机构信息

Departments of Immunology, Dermatology and Rheumatology, University Medical Center Utrecht, PO Box 85090, 3508 AB, Utrecht, The Netherlands.

出版信息

Clin Drug Investig. 2013 Apr;33(4):275-81. doi: 10.1007/s40261-013-0064-2.

Abstract

BACKGROUND

Recombinant human C1-inhibitor (rhC1INH) purified from milk of transgenic rabbits is used for the treatment of acute attacks in patients with hereditary angioedema (HAE) due to C1-inhibitor (C1INH) deficiency.

OBJECTIVE

The objective was to investigate the risk of rhC1INH inducing IgE antibodies or eliciting anaphylactic reactions.

METHODS

In subjects treated with rhC1INH, we retrospectively analysed the frequency and clinical relevance of pre-exposure and potentially newly induced IgE antibodies against rabbit and other animal allergens including cow's milk by the ImmunoCAP(®) Specific IgE blood test system.

RESULTS

130 HAE patients and 14 healthy subjects received 300 administrations of rhC1INH, 65 subjects (47.4 %) on one occasion; 72 (52.6 %) on at least two occasions (range 2-12; median 2). Five subjects had pre-existing anti-rabbit epithelium IgE; the subject with the highest levels and a previously undisclosed rabbit allergy developed an anaphylactic reaction upon first exposure to rhC1INH, whereas the other four subjects with lower pre-existing IgE levels (Class 1-3), did not. No other anaphylactic reactions were identified in any of the subjects exposed to rhC1INH. Analysis of post-exposure samples revealed that the risk of inducing new or boosting existing IgE responses to rabbit or cow's milk allergens was negligible.

CONCLUSION

The propensity of rhC1INH to induce IgE antibodies following repeated administration of rhC1INH is low. Subjects with substantially elevated anti-rabbit epithelium IgE antibodies and/or clinical allergy to rabbits may have an increased risk for an allergic reaction. No other risk factors for allergic reactions to rhC1INH have been identified.

摘要

背景

从转基因兔乳汁中纯化得到的重组人 C1 抑制剂(rhC1INH),被用于治疗因 C1 抑制剂(C1INH)缺乏导致的遗传性血管性水肿(HAE)急性发作的患者。

目的

本研究旨在探究 rhC1INH 是否会诱导 IgE 抗体产生或引发过敏反应。

方法

对接受 rhC1INH 治疗的患者,我们通过 ImmunoCAP(®)特异性 IgE 血检系统,对兔和其他动物过敏原(包括牛奶)的预暴露和潜在新诱导 IgE 抗体的频率及临床相关性进行回顾性分析。

结果

130 例 HAE 患者和 14 例健康对照者接受了 300 次 rhC1INH 治疗,其中 65 例(47.4%)仅接受 1 次治疗,72 例(52.6%)接受了至少 2 次治疗(范围 2-12 次;中位数 2 次)。5 例患者存在抗兔上皮 IgE;其中,该患者 IgE 水平最高且此前未披露存在兔过敏史,在首次接触 rhC1INH 时发生了过敏反应,而其他 4 例具有较低预存 IgE 水平(I 级-III 级)的患者则未发生过敏反应。在任何接受 rhC1INH 治疗的患者中均未发现其他过敏反应。暴露后样本分析显示,rhC1INH 重复给药后诱导新的或增强现有兔或牛奶过敏原 IgE 反应的风险可忽略不计。

结论

rhC1INH 多次给药后诱导 IgE 抗体产生的倾向较低。抗兔上皮 IgE 抗体水平显著升高且对兔过敏的患者,发生过敏反应的风险可能增加。尚未确定对 rhC1INH 产生过敏反应的其他危险因素。

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