Download as pdf or txt
Download as pdf or txt
You are on page 1of 1

S116 Abstracts J ALLERGY CLIN IMMUNOL

JANUARY 2007

456
GERMANY.
Basophil Activation In Food Allergic Patients
M. Worm; Dept. of Dermatology and Allergy, Berlin, 458 Epicutaneous Testing Using Peanut Extracts Prepared by a
Variety of Cooking Methods
M. Peng1, G. Hubbard1, J. A. Nordlee2, S. L. Hefle2, M. B. Levy1; 1Med-
RATIONALE: In recent studies the determination of the basophil activa- ical College of Wisconsin, Milwaukee, WI, 2University of Nebraska, Food
tion marker CD203c was found to be a novel diagnostic tool. In this study Allergy Research and Resource Program, Lincoln, NE.
we investigated in vivo basophil activation after oral provocation in food RATIONALE: The incidence of peanut allergy is higher in the United
allergic patients and determined the allergenicity of different processed States than in other countries, such as China, despite equal consumption.
food allergen extracts by in vitro analysis. This is theorized to occur, in part, because of differences in the way peanuts
METHODS: Samples were collected before and after the provocation for are prepared: roasted versus boiled and/or fried. Since cooking peanuts has
the determination of in vivo basophil activation. In vitro measurements been shown to change IgE binding in-vitro, we examined epicutaneous
were performed with patients’ blood samples. Cells were stimulated testing responses to peanuts prepared by a variety of cooking methods.
in vitro with different concentrations of food extracts. For determination METHODS: Extracts of dry roasted, boiled 20 minutes and one hour, oil
of basophil activation the CD203c expression was measured by flow cyto- roasted, fried, and raw peanuts were prepared. Each extract contained an
metric analysis and the data was analysed by ‘‘FACS Cell Quest’’ equal amount of protein. Thirty peanut allergic patients were skin prick
programme. tested with each peanut extract using a Multi-testÒ apparatus. Wheal
RESULTS: 59/73 studied patients had a low, but statistically significant size was measured and compared using two-tailed T test.
increase of in vivo CD203c expression after the oral provocation (21% RESULTS: Skin test reactions to oil roasted (p50.01), boiled one hour and
(6 3.2) to 26% (6 3.2); p<0.001). The in vitro analysis showed that a ba- 20 minutes (p50.03, p50.003), and dry roasted (p50.001) peanuts were
SUNDAY

sophil activation of 50% was reached at significant lower concentrations by significantly less than those to raw peanuts. Other comparisons were not
native compared to processed food extract. significantly different.
CONCLUSIONS: Our data suggests that CD203c expression may be used CONCLUSION: We observed that peanut extracts prepared by a variety
as an in vivo predictive marker for clinical relevant food allergy and is also of cooking methods decreased skin test reactivity as compared to raw pea-
useful for the determination of allergenicity in vitro. nut extract. This suggests that the preparation of peanuts by various cook-
Funding: BMBF ing methods may not contribute to the higher incidence of peanut allergy in
the United States.
457 Association Between Milk Allergy, Steroid Use, And Rate Of
Hospitalizations In Children With Asthma
A. B. Sympson1,2, E. Yousef1,2; 1DuPonts Children’s Hospital, Wilming- 459 Sunflower Seed Food Allergy as a Co-allergy With Peanut
S. S. Comstock, C. Kath, S. S. Teuber; Univ CA-Davis School
ton, DE, 2Thomas Jefferson Uiniversity, Philadlephia, PA. Medicine, Davis, CA.
RATIONALE: Asthma continues to be the leading cause of morbidity and RATIONALE: Sunflower seed allergens are not well-described. Because
mortality in the pediatric population. Studies have looked at the association sunflower seed butter may be consumed as an alternative to peanut butter
between food sensitization on asthma severity. We studied the effect milk by peanut-allergic individuals or those trying to avoid sensitization to pea-
allergy has on the number of hospitalizations and steroid use in asthmatic nut, issues of co-allergy are important.
children followed by an outpatient allergy practice. METHOD: Volunteers with self-reported severe nut and/or seed allergies
METHODS: Medical records of 197 children with diagnosis of asthma were recruited. Subjects were interviewed and asked if they had ever eaten
(ICD -9 codes 493.90, 493.91, and 493.92), aged 3 months to 14 years the following foods and if they had any symptoms upon ingestion: different
were reviewed. Of the 87 children with food allergy, 35 had allergy to tree nuts, peanut, sunflower seeds, pumpkin, or sesame seeds. Sera donated
milk (Group A). This group was compared with a 110 patients without by some subjects were used in IgE immunoblots against raw sunflower
any food allergy (Group B), for rate of hospitalizations and use of systemic seed extract and sunflower butter extract.
steroids. Study subjects were adjusted for the severity of asthma at presen- RESULTS: In our population of seed or nut-allergic individuals, co-
tation, presence of environmental allergy, atopic dermatitis, tobacco smoke allergy to peanut and sunflower seed was reported by 20 of 210 patients
exposure, and GERD. with peanut allergy (9.5%). Sera from patients with sunflower and peanut
RESULTS: Children with milk allergy had higher rate of hospitalizations allergy showed IgE binding to multiple sunflower polypeptide bands in
(p50.016) and increased use of systemic steroids (p50.001). both the seed and butter extracts. The roasted sunflower butter extract con-
CONCLUSIONS: Milk allergy was associated with increased hospitaliza- tained more high molecular weight polypeptides in a Coomassie-stained
tion rates and steroid use among children with asthma. Early identification gel. Much, but not all, of the IgE reactivity was absorbed out by preincu-
of food allergy in high risk patients and avoidance of offending food may bation of sera with perennial ryegrass pollen extract. 31 patients with pea-
be advisable for a better long term prognosis. nut allergy, but no known sunflower seed allergy were also screened (some
of whom had never eaten sunflower seeds), and 9 showed IgE binding to
sunflower proteins.
CONCLUSIONS: Some patients with peanut allergy are clinically aller-
gic to both peanut and sunflower by self-report. Also, a percentage of pa-
tients with peanut allergy have sunflower seed-reactive IgE that may not be
clinically relevant.
Funding: University of California, Davis

You might also like