Monitoring peanut allergen in food products by measuring Ara h 1

被引:78
作者
Pomés, A
Helm, RM
Bannon, GA
Burks, AW
Tsay, A
Chapman, MD
机构
[1] INDOOR Biotechnol Inc, Charlottesville, VA 22903 USA
[2] Arkansas Childrens Hosp, Res Inst, Dept Pediat, Little Rock, AR 72202 USA
关键词
peanut allergen; food allergy; immunoassay; environmental test;
D O I
10.1067/mai.2003.118
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Peanut allergy is an important health problem in the United States, affecting approximately 0.6% of children. Inadvertent exposure to peanut is a risk factor for life-threatening food-induced anaphylaxis. Objective: The purpose of this investigation was to develop an immunoassay for a major peanut allergen, Ara h 1, to detect peanut allergen in foods so that the risk of inadvertent exposure can be reduced. Methods: A specific 2-site monoclonal antibody-based ELISA was developed to measure Ara h 1 in foods. The sensitivity of the assay was 30 ng/mL. Ara h I was measured in foods (n 83) with or without peanut and in experiments to optimize allergen yield and to determine peanut contamination in spiked foods. Results: Ara h I levels in food products ranged from less than 0.1 mug/g to 500 mug/g. Ara h 1 measured in ng/mL was transformed to mug/g for food products. Peanut butter contained the highest amounts of Ara h 1. Peanut extracts contained from 0.5 to 15 mg Ara h 1/g of peanut depending on the extraction conditions. Optimal extraction of Ara h 1 was obtained by using phosphate buffer with 1 mol/L NaCl and Tween at 60degreesC. Ara h 1 was not always detected in presence of chocolate under the extraction conditions tested. Spiking experiments showed that the assay could detect similar to0.1% Ara h I contamination of food with ground peanut. There was an excellent correlation between Ara h 1 levels and peanut content measured by using a commercial polyclonal antibody-based ELISA (r = 93, n = 31, P <.001). Conclusion: A new sensitive and specific monoclonal antibody-based ELISA was used to monitor Ara h 1 content in food products. This assay should be useful for monitoring peanut contamination in the food manufacturing and processing industry and in developing thresholds for sensitization or allergic reaction in persons with peanut allergy.
引用
收藏
页码:640 / 645
页数:6
相关论文
共 40 条
[1]  
Bando N, 1998, J NUTR SCI VITAMINOL, V44, P655, DOI 10.3177/jnsv.44.655
[2]   Soybean glycinin G1 acidic chain shares IgE epitopes with peanut allergen Ara h 3 [J].
Beardslee, TA ;
Zeece, MG ;
Sarath, G ;
Markwell, JP .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2000, 123 (04) :299-307
[3]   CROSS-ALLERGENICITY IN THE LEGUME BOTANICAL FAMILY IN CHILDREN WITH FOOD HYPERSENSITIVITY [J].
BERNHISELBROADBENT, J ;
SAMPSON, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (02) :435-440
[4]   CROSS-ALLERGENICITY IN THE LEGUME BOTANICAL FAMILY IN CHILDREN WITH FOOD HYPERSENSITIVITY .2. LABORATORY CORRELATES [J].
BERNHISELBROADBENT, J ;
TAYLOR, S ;
SAMPSON, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 84 (05) :701-709
[5]   Effects of cooking methods on peanut allergenicity [J].
Beyer, KB ;
Morrow, E ;
Li, XM ;
Bardina, L ;
Bannon, GA ;
Burks, AW ;
Sampson, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (06) :1077-1081
[6]   Fatalities due to anaphylactic reactions to foods [J].
Bock, SA ;
Muñoz-Furlong, A ;
Sampson, HA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (01) :191-193
[7]   IDENTIFICATION OF A MAJOR PEANUT ALLERGEN, ARA-H-I, IN PATIENTS WITH ATOPIC-DERMATITIS AND POSITIVE PEANUT CHALLENGES [J].
BURKS, AW ;
WILLIAMS, LW ;
HELM, RM ;
CONNAUGHTON, C ;
COCKRELL, G ;
OBRIEN, T .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1991, 88 (02) :172-179
[8]   RECOMBINANT PEANUT ALLERGEN ARA-H-I EXPRESSION AND IGE BINDING IN PATIENTS WITH PEANUT HYPERSENSITIVITY [J].
BURKS, AW ;
COCKRELL, G ;
STANLEY, JS ;
HELM, RM ;
BANNON, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) :1715-1721
[9]   ALLERGENICITY OF PEANUT AND SOYBEAN EXTRACTS ALTERED BY CHEMICAL OR THERMAL-DENATURATION IN PATIENTS WITH ATOPIC-DERMATITIS AND POSITIVE FOOD CHALLENGES [J].
BURKS, AW ;
WILLIAMS, LW ;
THRESHER, W ;
CONNAUGHTON, C ;
COCKRELL, G ;
HELM, RM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 90 (06) :889-897
[10]  
CHANG JH, 1995, METHOD ENZYMOL, V254, P430