Paediatrics (RCH) - Research Publications

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    B-cell phenotype and function in infants with egg allergy
    Neeland, MR ; Martino, DJ ; Dang, TD ; Koplin, JJ ; Peters, RL ; Grishin, A ; Dharmage, SC ; Tang, ML ; Sampson, HA ; Saffery, R ; Allen, KJ (WILEY, 2019-05)
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    Egg allergen specific IgE diversity predicts resolution of egg allergy in the population cohort HealthNuts
    Dang, TD ; Peters, RL ; Koplin, JJ ; Dharmage, SC ; Gurrin, LC ; Ponsonby, A-L ; Martino, DJ ; Neeland, M ; Tang, MLK ; Allen, KJ (WILEY, 2019-02)
    BACKGROUND: IgE-mediated egg allergy presents as one of the most common food allergies in children. Measurement of egg white specific IgE (sIgE) levels in serum or skin prick test has been shown to be a poor predictor of clinical allergy to raw egg white, and also to baked or cooked egg. Recent developments in component resolved diagnostic (CRD) technology have enabled us to improve the way in which we diagnose and predict peanut allergy by examining IgE specificity to individual peptides. OBJECTIVES: We aimed to investigate whether egg CRD could improve current methods to diagnose various egg allergy phenotypes as well as predict the development of tolerance to egg. METHODS: Using the HealthNuts cohort of food challenge-proven egg allergic and egg-sensitized and egg-tolerant, age-matched 12-month infants with longitudinal follow-up at 2 and 4 years (n = 451), we measured serum egg white, Gal d 1, 2, 3 and 5 sIgE using ImmunoCAP. RESULTS: Gal d 1 sensitization increased the risk of persistent egg allergy by 2.5-fold. The production of sIgE to all four egg allergens (Gal d 1, 2, 3 or 5) increased the risk of having persistent raw egg allergy fourfold (OR 4.19 (95% CI: 1.25-14.07). We did not find any improvements of using Gal d 1, 2, 3 or 5 to diagnose current egg allergy compared to egg white sIgE. CONCLUSION: Sensitization to multiple egg allergens Gal d 1, 2, 3 or 5 may be a prognostic marker that could be useful for patient management and identifying individuals at risk of developing persistent egg allergy.
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    The Impact of Family History of Allergy on Risk of Food Allergy: A Population-Based Study of Infants
    Koplin, JJ ; Allen, KJ ; Gurrin, LC ; Peters, RL ; Lowe, AJ ; Tang, MLK ; Dharmage, SC (MDPI AG, 2013-11)
    The apparent rapid increase in IgE-mediated food allergy and its implications are now widely recognized, but little is known about the relationship between family history (an indirect measure of genetic risk) and the risk of food allergy. In a population-based study of 5,276 one year old infants (HealthNuts), the prevalence of oral food challenge-confirmed food allergy was measured. Associations between family history of allergic disease and food allergy in infants were examined using multiple logistic regression. Food allergy was diagnosed in 534 infants. Compared to those with no family history of allergic disease, children meeting the current definition of "high risk" for allergic disease (one immediate family member with a history of any allergic disease) showed only a modest increase (OR 1.4, 95% CI 1.1-1.7) in food allergy, while having two or more allergic family members was more strongly predictive of food allergy in the child (OR 1.8, 95% CI 1.5-2.3). There were also differences in the associations between family history and egg and peanut allergy in the child. Re-defining "high risk" as two or more allergic family members may be more useful for identification of groups with a significantly increased risk of food allergy both clinically and within research studies.
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    Filaggrin loss-of-function mutations do not predict food allergy over and above the risk of food sensitization among infants
    Tan, H-TT ; Ellis, JA ; Koplin, JJ ; Matheson, MC ; Gurrin, LC ; Lowe, AJ ; Martin, PE ; Dang, TD ; Wake, M ; Tang, MLK ; Ponsonby, A-L ; Dharmage, SC ; Allen, KJ (MOSBY-ELSEVIER, 2012-11)