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Wiley InterScience | ||
![]() Clinical & Experimental AllergyVolume 31 Issue 10, Pages 1599 - 1606 Published Online: 7 Jul 2008 © 2010 Blackwell Publishing Ltd The Official Journal of the British Society for Allergy & Clinical Immunology
Abstract | References | Full Text: HTML, PDF (Size: 454K) | Related Articles | Citation Tracking Role of conformational and linear epitopes in the achievement of tolerance in cow's milk allergy Copyright Blackwell Science Ltd KEYWORDS cow's milk allergy • tolerance • epitope • conformational • linear • α ABSTRACTBackgroundCow's milk (CM) is one of the leading causes of food allergy in children. However, approximately 85% of milk-allergic children become clinically tolerant to CM within the first 3 years of life. The mechanisms involved in the achievement of tolerance remain unknown. ObjectiveObjectiveTo study whether IgE antibodies from children with persistent cow's milk allergy (CMA) differ from children who become clinically tolerant in their ability to recognize linear and conformational epitopes of α MethodsMethodsThirty-six milk-allergic children were included in the study: 11 of the children became clinically tolerant, and 25 had persistent CMA. Blood was obtained from all patients during the time they showed clinical reactions to milk challenge. Six non-milk-allergic children served as controls. Specific IgE antibodies against linear (denatured) as well as conformational (native) milk proteins were determined by probing dot-blots with patients' sera. In addition, selected decapeptides from α ResultsResultsAnalysis of immunodot-blots showed that, in comparison to tolerant patients, milk-allergic children with persistent symptoms had a significantly higher ratio of specific IgE antibodies to linearized than to native α- and β-casein (P < 0.005 and P < 0.02, respectively). Comparing the selected decapeptides, six of the 10 patients with persistent allergy recognized the peptide corresponding to amino acids 69–78 from α ConclusionConclusionPatients with persistent milk allergy possess higher detectable levels of IgE antibodies to linear epitopes from α Submitted 21 August 2000; revised 20 March; accepted 30 April 2001. |