IgE to peanut allergen components: relation to peanut symptoms and pollen sensitization in 8-year-olds

被引:102
|
作者
Asarnoj, A. [1 ,2 ]
Moverare, R. [3 ,4 ]
Ostblom, E. [5 ,6 ,7 ]
Poorafshar, M. [3 ]
Lilja, G. [5 ]
Hedlin, G. [2 ,6 ]
van Hage, M. [8 ,9 ]
Ahlstedt, S. [1 ,6 ]
Wickman, M. [1 ,5 ,6 ]
机构
[1] Karolinska Inst, Natl Inst Environm Med, SE-17177 Stockholm, Sweden
[2] Astrid Lindgrens Childrens Hosp, Dept Paediat, Stockholm, Sweden
[3] Phadia AB, Uppsala, Sweden
[4] Uppsala Univ, Dept Med Sci Resp Med & Allergol, Uppsala, Sweden
[5] Karolinska Inst, Sachs Childrens Hosp, Dept Paediat, Stockholm, Sweden
[6] Karolinska Inst, Ctr Allergy Res, SE-17177 Stockholm, Sweden
[7] Karolinska Inst, Dept Clin Sci & Educ, SE-17177 Stockholm, Sweden
[8] Karolinska Inst, Dept Med, Allergy & Clin Immunol Unit, SE-17177 Stockholm, Sweden
[9] Univ Hosp, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
allergen components; BAMSE; childhood; IgE; peanut; FOOD ALLERGY; ANAPHYLACTIC REACTIONS; CROSS-REACTIVITY; BIRCH POLLEN; BIRTH COHORT; ARA H2; CHILDREN; LIFE; PREVALENCE; DIAGNOSIS;
D O I
10.1111/j.1398-9995.2010.02334.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Allergen-specific IgE testing is often performed with crude peanut extract, but the results may be difficult to interpret because of cross-reactions between peanut and other plant allergens. The aim was to investigate IgE reactivity to peanut allergen components in children from a birch-rich region in relation to pollen sensitization and peanut symptoms. Methods: From a birth cohort, clinical parameters were obtained through questionnaires and IgE antibody levels to peanut and birch pollen were measured. Different peanut/birch sensitization phenotypes were defined among 200 selected children. IgE reactivity to peanut and pollen allergen components was analysed using microarray technique. Results: Peanut symptoms were reported in 87% of the children with IgE reactivity to any of the peanut allergens Ara h 1, 2 or 3 but not to Ara h 8 (n = 46) vs 17% of children with IgE reactivity to Ara h 8 but not to Ara h 1, 2 or 3 (n = 23), P < 0.001. Furthermore, symptoms were more severe in children with Ara h 1, 2 or 3 reactivity. Children with IgE reactivity both to Ara h 2 and to Ara h 1 or 3 more often reported peanut symptoms than children with IgE only to Ara h 2 (97% vs 70%, P = 0.016), particularly respiratory symptoms (50% vs 9%, P = 0.002). Conclusions: IgE analysis to peanut allergen components may be used to distinguish between peanut-sensitized individuals at risk of severe symptoms and those likely to have milder or no symptoms to peanut if sensitized to pollen allergens and their peanut homologue allergens.
引用
收藏
页码:1189 / 1195
页数:7
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