Safety of a peanut oral immunotherapy protocol in children with peanut allergy

被引:220
|
作者
Hofmann, Alison M. [1 ]
Scurlock, Amy M. [2 ]
Jones, Stacie M. [2 ]
Palmer, Kricia P. [2 ]
Lokhnygina, Yuliya [3 ]
Steele, Pamela H. [1 ]
Kamilaris, Janet [1 ]
Burks, A. Wesley [1 ]
机构
[1] Duke Univ, Med Ctr, Div Allergy & Immunol, Dept Pediat, Durham, NC 27710 USA
[2] Univ Arkansas, Dept Pediat, Div Allergy & Immunol, Little Rock, AR 72204 USA
[3] Duke Univ, Dept Biostat & Bioinformat, Durham, NC 27706 USA
基金
美国国家卫生研究院;
关键词
Peanut; food allergy; oral immunotherapy; TOLERANCE INDUCTION; FOOD; DESENSITIZATION;
D O I
10.1016/j.jaci.2009.03.045
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Oral immunotherapy (OIT) offers a promising therapeutic option for peanut allergy. Given that during OIT an allergic patient ingests an allergen that could potentially cause a serious reaction, the safety of OIT is of particular concern. Objective: The purpose of this study was to examine safety during the initial escalation day, buildup phase, and home dosing phase in subjects enrolled in a peanut OIT study. Methods: Skin, upper respiratory tract, chest, and abdominal symptoms were recorded with initial escalation day and buildup phase dosings. Subjects also maintained daily diaries detailing symptoms after each home dosing. A statistical analysis of these data was performed. Results: Twenty of 28 patients completed all phases of the study. During the initial escalation day, upper respiratory tract (79%) and abdominal (68%) symptoms were the most likely symptoms experienced. The risk of mild wheezing during the initial escalation day was 18%. The probability of having any symptoms after a buildup phase dose was 46%, with a risk of 29% for upper respiratory tract symptoms and 24% for skin symptoms. The risk of reaction with any home dose was 3.5%. Upper respiratory tract (1.2%) and skin (1.1%) symptoms were the most likely after home doses. Treatment was given with 0.7% of home doses. Two subjects received epinephrine after I home dose each. Conclusions: Subjects were more likely to have significant allergic symptoms during the initial escalation day when they were in a closely monitored setting than during other phases of the study. Allergic reactions with home doses were rare. (J Allergy Clin Immunol 2009;124:286-91.)
引用
收藏
页码:286 / 291
页数:6
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