Boston Children's Hospital and Harvard Medical School, Boston, Mass.
J Allergy Clin Immunol. 2013 Dec;132(6):1368-74. doi: 10.1016/j.jaci.2013.09.046. Epub 2013 Oct 28.
Peanut allergy is a major public health problem that affects 1% of the population and has no effective therapy.
To examine the safety and efficacy of oral desensitization in peanut-allergic children in combination with a brief course of anti-IgE mAb (omalizumab [Xolair]).
We performed oral peanut desensitization in peanut-allergic children at high risk for developing significant peanut-induced allergic reactions. Omalizumab was administered before and during oral peanut desensitization.
We enrolled 13 children (median age, 10 years), with a median peanut-specific IgE level of 229 kU(A)/L and a median total serum IgE level of 621 kU/L, who failed an initial double-blind placebo-controlled food challenge at peanut flour doses of 100 mg or less. After pretreatment with omalizumab, all 13 subjects tolerated the initial 11 desensitization doses given on the first day, including the maximum dose of 500 mg peanut flour (cumulative dose, 992 mg, equivalent to >2 peanuts), requiring minimal or no rescue therapy. Twelve subjects then reached the maximum maintenance dose of 4000 mg peanut flour per day in a median time of 8 weeks, at which point omalizumab was discontinued. All 12 subjects continued on 4000 mg peanut flour per day and subsequently tolerated a challenge with 8000 mg peanut flour (equivalent to about 20 peanuts), or 160 to 400 times the dose tolerated before desensitization. During the study, 6 of the 13 subjects experienced mild or no allergic reactions, 5 subjects had grade 2 reactions, and 2 subjects had grade 3 reactions, all of which responded rapidly to treatment.
Among children with high-risk peanut allergy, treatment with omalizumab may facilitate rapid oral desensitization and qualitatively improve the desensitization process.
花生过敏是一个严重的公共卫生问题,影响 1%的人群,目前尚无有效的治疗方法。
评估口服脱敏联合奥马珠单抗(Xolair)治疗花生过敏儿童的安全性和疗效。
我们对有发生严重花生诱导过敏反应风险的花生过敏儿童进行口服花生脱敏治疗。奥马珠单抗在口服脱敏治疗前和治疗期间使用。
我们纳入了 13 名儿童(中位年龄 10 岁),花生特异性 IgE 水平中位数为 229 kU(A)/L,总血清 IgE 水平中位数为 621 kU/L,他们在最初的花生粉剂量为 100mg 或更低的双盲安慰剂对照食物挑战中失败。奥马珠单抗预处理后,所有 13 名受试者均能耐受第 1 天给予的最初 11 次脱敏剂量,包括最大剂量 500mg 花生粉(累计剂量 992mg,相当于>2 颗花生),仅需最小剂量或无需抢救治疗。12 名受试者随后在中位时间 8 周内达到每天 4000mg 花生粉的最大维持剂量,此时停用奥马珠单抗。所有 12 名受试者继续每天服用 4000mg 花生粉,随后耐受 8000mg 花生粉(相当于约 20 颗花生)的挑战,或耐受脱敏前剂量的 160-400 倍。研究期间,13 名受试者中有 6 名出现轻度或无过敏反应,5 名出现 2 级反应,2 名出现 3 级反应,所有反应均迅速得到治疗。
在高风险花生过敏儿童中,奥马珠单抗治疗可能促进快速口服脱敏,并在质量上改善脱敏过程。