Department of Pediatric Pneumology and Immunology, University Hospital Charité, Berlin, Germany.
J Allergy Clin Immunol. 2010 Jul;126(1):83-91.e1. doi: 10.1016/j.jaci.2010.04.030. Epub 2010 Jun 12.
The only treatment option for peanut allergy is strict avoidance.
To investigate efficacy and safety of oral immunotherapy (OIT) in peanut allergy.
Twenty-three children (age, 3.2-14.3 years) with IgE-mediated peanut allergy confirmed by positive double-blind, placebo-controlled food challenge (DBPCFC) received OIT following a rush protocol with roasted peanut for 7 days. If a protective dose of at least 0.5 g peanut was not achieved, patients continued with a long-term buildup protocol using biweekly dose increases up to at least 0.5 g peanut. A maintenance phase for 8 weeks was followed by 2 weeks of peanut avoidance and a final DBPCFC. Immunologic parameters were determined.
After OIT using the rush protocol, patients tolerated a median dose of only 0.15 g peanut. Twenty-two of 23 patients continued with the long-term protocol. After a median of 7 months, 14 patients reached the protective dose. At the final DBPCFC, patients tolerated a median of 1 g (range, 0.25-4 g) in comparison with 0.19 g peanut at the DBPCFC before OIT (range, 0.02-1 g). In 2.6% of 6137 total daily doses, mild to moderate side effects were observed; in 1.3%, symptoms of pulmonary obstruction were detected. OIT was discontinued in 4 of 22 patients because of adverse events. There was a significant increase in peanut-specific serum IgG(4) and a decrease in peanut-specific IL-5, IL-4, and IL-2 production by PBMCs after OIT.
Long-term OIT appears to be safe and of some benefit in many patients with peanut allergy. With an increase in threshold levels and a reduction of peanut-specific T(H)2 cytokine production, the induction of tolerance may be feasible in some patients.
目前针对花生过敏的唯一治疗方法是严格避免接触花生。
研究口服免疫疗法(OIT)在花生过敏中的疗效和安全性。
23 例 IgE 介导的花生过敏患儿(年龄 3.2-14.3 岁),通过双盲、安慰剂对照食物激发试验(DBPCFC)证实为阳性,采用速发型方案,7 天内给予烤花生。如果未能达到至少 0.5g 花生的保护剂量,则患者继续采用长程增量方案,每两周增加剂量,直至达到至少 0.5g 花生。随后进行 8 周的维持期,接着进行 2 周的花生回避期,最后进行最终的 DBPCFC。测定免疫参数。
采用速发型方案进行 OIT 后,患者仅能耐受中位数剂量 0.15g 花生。23 例患者中有 22 例继续进行长程方案。中位时间 7 个月后,14 例患者达到保护剂量。在最终的 DBPCFC 中,患者耐受中位数剂量 1g(范围,0.25-4g),而 OIT 前 DBPCFC 中仅耐受 0.19g 花生(范围,0.02-1g)。在 6137 总日剂量中,观察到 2.6%出现轻度至中度副作用;1.3%出现阻塞性肺症状。因不良事件,22 例患者中有 4 例停止 OIT。OIT 后,花生特异性血清 IgG4 显著增加,PBMC 中花生特异性 IL-5、IL-4 和 IL-2 产生减少。
长期 OIT 似乎对许多花生过敏患者是安全且有益的。随着阈值水平的提高和花生特异性 T(H)2 细胞因子产生的减少,在某些患者中诱导耐受可能是可行的。