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

Journal Article (Journal Article)

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 IgGâ‚„ 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.

Full Text

Duke Authors

Cited Authors

  • Vickery, BP; Scurlock, AM; Kulis, M; Steele, PH; Kamilaris, J; Berglund, JP; Burk, C; Hiegel, A; Carlisle, S; Christie, L; Perry, TT; Pesek, RD; Sheikh, S; Virkud, Y; Smith, PB; Shamji, MH; Durham, SR; Jones, SM; Burks, AW

Published Date

  • February 2014

Published In

Volume / Issue

  • 133 / 2

Start / End Page

  • 468 - 475

PubMed ID

  • 24361082

Pubmed Central ID

  • PMC3960331

Electronic International Standard Serial Number (EISSN)

  • 1097-6825

Digital Object Identifier (DOI)

  • 10.1016/j.jaci.2013.11.007


  • eng

Conference Location

  • United States