Sustained unresponsiveness to peanut in subjects who have completed peanut oral immunotherapy.

Brian P Vickery, Amy M Scurlock, Michael Kulis, Pamela H Steele, Janet Kamilaris, Jelena P Berglund, Caitlin Burk, Anne Hiegel, Suzanna Carlisle, Lynn Christie, Tamara T Perry, Robbie D Pesek, Saira Sheikh, Yamini Virkud, P Brian Smith, Mohamed H Shamji, Stephen R Durham, Stacie M Jones, A Wesley Burks

Journal: The Journal of allergy and clinical immunology 2014;133(2):468-75

PMID: 24361082

Abstract

BACKGROUND

Although peanut oral immunotherapy (OIT) has been conclusively shown to cause desensitization, it is currently unknown whether clinical protection persists after stopping therapy.

OBJECTIVE

Our primary objective was to determine whether peanut OIT can induce sustained unresponsiveness after withdrawal of OIT.

METHODS

We conducted a pilot clinical trial of peanut OIT at 2 US centers. Subjects age 1 to 16 years were recruited and treated for up to 5 years with peanut OIT. The protocol was modified over time to permit dose increases to a maximum of 4000 mg/d peanut protein. Blood was collected at multiple time points. Clinical end points were measured with 5000-mg double-blinded, placebo-controlled food challenges once specific criteria were met.

RESULTS

Of the 39 subjects originally enrolled, 24 completed the protocol and had evaluable outcomes. Twelve (50%) of 24 successfully passed a challenge 1 month after stopping OIT and achieved sustained unresponsiveness. Peanut was added to the diet. At baseline and the time of challenge, such subjects had smaller skin test results, as well as lower IgE levels specific for peanut, Ara h 1, and Ara h 2 and lower ratios of peanut-specific IgE/total IgE compared with subjects not passing. There were no differences in peanut IgG₄ levels or functional activity at the end of the study.

CONCLUSIONS

This is the first demonstration of sustained unresponsiveness after peanut OIT, occurring in half of subjects treated for up to 5 years. OIT favorably modified the peanut-specific immune response in all subjects completing the protocol. Smaller skin test results and lower allergen-specific IgE levels were predictive of successful outcome.

Copyright © 2013 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.

Address: Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC. Electronic address: [email protected].; Department of Pediatrics, University of Arkansas for Medical Sciences and Arkansas Children's Hospital, Little Rock, Ark.; Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC.; Duke Translational Medicine Institute, Durham, NC.; Department of Pediatrics, Duke University School of Medicine, Durham, NC.; Section of Allergy and Clinical Immunology, National Heart and Lung Institute, Imperial College, London, United Kingdom.
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