Allergen specificity of early peanut consumption and effect on development of allergic disease in the Learning Early About Peanut Allergy study cohort - 05/04/18
for the
Immune Tolerance Network Learning Early About Peanut Allergy study team
Abstract |
Background |
Early introduction of dietary peanut in high-risk infants with severe eczema, egg allergy, or both prevented peanut allergy at 5 years of age in the Learning Early About Peanut Allergy (LEAP) study. The protective effect persisted after 12 months of avoiding peanuts in the 12-month extension of the LEAP study (LEAP-On). It is unclear whether this benefit is allergen and allergic disease specific.
Objective |
We sought to assess the effect of early introduction of peanut on the development of allergic disease, food sensitization, and aeroallergen sensitization.
Methods |
Asthma, eczema, and rhinoconjunctivitis were diagnosed based on clinical assessment. Reported allergic reactions and consumption of tree nuts and sesame were recorded by questionnaire. Sensitization to food allergens and aeroallergens was determined by means of skin prick testing and specific IgE measurement.
Results |
A high and increasing burden of food allergen and aeroallergen sensitization and allergic disease was noted across study time points; 76% of LEAP participants had at least 1 allergic disease at 60 months of age. There were no differences in allergic disease between LEAP groups. There were small differences in sensitization and reported allergic reactions for select tree nuts, with levels being higher in the LEAP consumption group. Significant resolution of eczema and sensitization to egg and milk occurred in LEAP participants and was not affected by peanut consumption.
Conclusion |
Early consumption of peanut in infants at high risk of peanut allergy is allergen specific and does not prevent the development of other allergic disease, sensitization to other food allergens and aeroallergens, or reported allergic reactions to tree nuts and sesame. Furthermore, peanut consumption does not hasten the resolution of eczema or egg allergy.
Le texte complet de cet article est disponible en PDF.Graphical Abstract |
Key words : Food allergy, peanut allergy, allergy prevention, allergen-specific asthma, eczema, atopic dermatitis, rhinoconjunctivitis, tolerance
Abbreviations used : ITT, LEAP, LEAP-On, PP, SPT
Plan
Research reported in this publication was supported by the National Institute of Allergy and Infectious Diseases/National Institutes of Health (NIH) under award numbers NO1-AI-15416, UM1AI109565, HHSN272200800029C, and UM2AI117870. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. Additional support came from Food Allergy Research & Education (FARE), McLean, Va; the Medical Research Council & Asthma UK Centre; the UK Department of Health through the National Institute for Health Research (NIHR) comprehensive Biomedical Research Centre award to Guy's & St. Thomas' NHS Foundation Trust in partnership with King's College London and King's College Hospital NHS Foundation Trust. The clinical trials unit is supported by the National Peanut Board, Atlanta, Ga. The UK Food Standards Agency provided additional support for the costs of phlebotomy. G.L. acknowledges the Davis Foundation for academic support. |
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Disclosure of potential conflict of interest: G. du Toit reports income from grants from the National Institute of Allergy and Infectious Diseases (NIAID)/National Institutes of Health (NIH), Food Allergy & Research Education (FARE), MRC & Asthma UK Centre, UK Department of Health through the National Institute of Health Research (NIHR), and the National Peanut Board (NPB) and grants from the UK Food Standards Agency (FSA; these grants part funded a salary over the period of this submitted work), and he has equity holding with FoodMaestro. P. H. Sayre has received a grant from the NIH. G. Roberts has received a grant from the Immune Tolerance Network. K. Lawson and M. L. Sever have received grants from the NIAID/NIH (UM2AI117870) and DAIT-SACCC and have received fees for participation in review activities and payment for manuscript preparation from the NIAID/NIH (contract no. HHSN272200800029C). H. T. Bahnson has received a grant from Rho (UM2AI117870) and the Benaroya Research Institute, ITN (UM1AI109565). H. R. Fisher, S. Radulovic, and M. Basting have received grants from the NIAID (NO1-AI-15416 [contract] and UM1AI109565 [grant]) and the FSA and have received other support from FARE, MRC & Asthma UK Centre, UK Department of Health through NIHR, National Peanut Board, and Osem. G. Lack has received grants from the NIAID (NO1-AI-15416 [contract] and UM1AI109565 [grant]), the FSA, FARE, MRC & Asthma UK Centre, UK Department of Health through NIHR, National Peanut Board, and Osem and has consultant arrangements and stock/stock options with DBV Technologies. M. Feeney has received grants from the NIAID (NO1-AI-15416 [contract] and UM1AI109565 [grant]) and the FSA and has received other support from FARE, MRC & Asthma UK Centre, UK Department of Health through the NIHR, National Peanut Board, and Osem; has consultant arrangements with Aimmune Therapeutics UK Limited; and has received payment for lectures from Nutricia Advanced Medical Nutrition. The rest of the authors declare that they have no relevant conflicts of interest. |
Vol 141 - N° 4
P. 1343-1353 - avril 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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