Abstract

The effects of epicutaneous allergen administration on systemic immune responses in allergic and non-allergic individuals has not been investigated with defined allergen molecules. We studied the effects of epicutaneous administration of rBet v 1 and rBet v 1 fragments on systemic immune responses in allergic and non-allergic subjects. We conducted a clinical trial in which rBet v 1 and two hypoallergenic rBet v 1 fragments were applied epicutaneously by atopy patch testing (APT) to 15 birch pollen (bp) allergic patients suffering from atopic dermatitis, 5 bp-allergic patients suffering from rhinoconjunctivitis only, 5 patients with respiratory allergy without bp allergy and 5 non-allergic individuals. Epicutaneous administration of rBet v 1 and rBet v 1 fragments led to strong and significant increases of allergen-specific T cell proliferation (CLA+ and CCR4+T cell responses) only in bp-allergic patients with a positive APT reaction. There were no relevant changes of Bet v 1-specific IgE and IgG responses. No changes were noted in allergic subjects without bp allergy and in non-allergic subjects. Epicutaneous allergen application boosts specific T cell but not antibody responses mainly in allergic, APT-positive patients suggesting IgE-facilitated allergen presentation as mechanism for its effects on systemic allergen-specific immune responses.

Highlights

  • Epicutaneous allergen administration in the form of atopy patch testing (APT) has been widely used to reveal T cell-mediated late phase allergic inflammation in patients suffering from atopic dermatitis[1]

  • It could be shown by APT that non-IgE-reactive Bet v 1 derivatives induced T cell mediated late phase skin inflammation in atopic dermatitis (AD) patients[5]

  • We showed that such reactions are very common and may explain the frequent occurrence of late phase reactions observed during allergen-specific immunotherapy (AIT) with T cell epitope-containing allergen derivatives[6]

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Summary

Introduction

Epicutaneous allergen administration in the form of atopy patch testing (APT) has been widely used to reveal T cell-mediated late phase allergic inflammation in patients suffering from atopic dermatitis[1]. We investigated if late-phase side effects observed in the course of AIT with recombinant non-IgE-reactive, T cell epitope-containing derivatives of the major birch pollen allergen Bet v 1 may be caused by a T cell-dependent and IgE-independent mechanism[4]. Only the effects of intranasal administration of recombinant allergens and hypoallergenic allergen derivatives on systemic immune responses in allergic patients have been investigated[7, 8] These studies showed that a single intranasal. We investigated the effects of epicutaneous application of the IgE-reactive recombinant form of the major birch pollen allergen, rBet v 1 (aa: 1–160) and two recombinant hypoallergenic rBet v 1 fragments (F1: aa 1–74, F2: aa 75–160)[9] on systemic allergen-specific antibody, T cell and cytokine responses

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