Epicutaneous Immunotherapy for the Treatment of Peanut Allergy in Children and Young Adults

Publication Type
Journal Article
Year of Publication
2017
Authors
Jones, SM; Sicherer, SH; Burks, AW; Leung, DYM; Lindblad, RW; Dawson, P; Henning, AK; Berin, MC; Chiang, D; Vickery, BP; Pesek, RD; Cho, CB; Davidson, WF; Plaut, M; Sampson, HA; Wood, RA; The Consortium of Food Allergy Research (CoFAR)
Secondary
J Allergy Clin Immunol
Volume
133
Start Page
1242
Pagination
1242-1252.e9
Date Published
04/2017
Keywords
CoFAR; desensitization; epicutaneous; food allergy; IgE; Immunotherapy; Peanut Hypersensitivity
Abstract

Background

Peanut allergy is common, life-threatening, and without therapeutic options. We evaluated peanut epicutaneous immunotherapy (EPIT) by using Viaskin Peanut for peanut allergy treatment.

Objective

We sought to evaluate the clinical, safety, and immunologic effects of EPIT for the treatment of peanut allergy.

Methods

In this multicenter, double-blind, randomized, placebo-controlled study, 74 participants with peanut allergy (ages 4-25 years) were treated with placebo (n = 25), Viaskin Peanut 100 μg (VP100; n = 24) or Viaskin Peanut 250 μg (VP250; n = 25; DBV Technologies, Montrouge, France). The primary outcome was treatment success after 52 weeks, which was defined as passing a 5044-mg protein oral food challenge or achieving a 10-fold or greater increase in successfully consumed dose from baseline to week 52. Adverse reactions and mechanistic changes were assessed.

Results

At week 52, treatment success was achieved in 3 (12%) placebo-treated participants, 11 (46%) VP100 participants, and 12 (48%) VP250 participants (P = .005 and P = .003, respectively, compared with placebo; VP100 vs VP250, P = .48). Median change in successfully consumed doses were 0, 43, and 130 mg of protein in the placebo, VP100, and VP250 groups, respectively (placebo vs VP100, P = .014; placebo vs VP250, P = .003). Treatment success was higher among younger children (P = 0.03; age, 4-11 vs >11 years). Overall, 14.4% of placebo doses and 79.8% of VP100 and VP250 doses resulted in reactions, predominantly local patch-site and mild reactions (P = .003). Increases in peanut-specific IgG4 levels and IgG4/IgE ratios were observed in peanut EPIT-treated participants, along with trends toward reduced basophil activation and peanut-specific TH2 cytokines.

Conclusions

Peanut EPIT administration was safe and associated with a modest treatment response after 52 weeks, with the highest responses among younger children. This, when coupled with a high adherence and retention rate and significant changes in immune pathways, supports further investigation of this novel therapy.