Daniel Lozano‐Ojalvo,Scott R. Tyler,Carlos J. Aranda,Julie Wang,Scott H. Sicherer,Hugh A. Sampson,Robert A. Wood,A. Wesley Burks,Stacie M. Jones,Donald Y.M. Leung,Maria Curotto de Lafaille,M. Cecilia Berin
出处
期刊:Cold Spring Harbor Laboratory - medRxiv日期:2022-05-17被引量:9
Abstract Type 2 allergen-specific T cells are essential for the induction and maintenance of allergies to foods, and Tregs specific for these allergens are assumed to be involved in their resolution. However, it has not been convincingly demonstrated whether allergen-specific Treg responses are responsible for the generation of oral tolerance in humans. We observed that sustained food allergen exposure in the form of oral immunotherapy resulted in increased frequency of Tregs only in individuals with lasting clinical tolerance. We sought to identify regulatory components of the CD4 + T cell response to food allergens by studying their functional activation over time in vitro and in vivo . Two subsets of Tregs expressing CD137 or CD25/OX40 were identified with a delayed kinetics of activation compared to clonally enriched pathogenic effector Th2 cells. Treg activation was dependent on IL-2 derived from effector T cells. In vivo exposure to peanut in the form of an oral food challenge of allergic subjects induced a delayed and persistent activation of Tregs after initiation of the allergen-specific Th2 response. Our results reveal a dependency of Tregs on effector Th2 cells for their activation and highlight the important role of IL-2 in the generation of a regulatory response to food allergens. One Sentence Summary Initiation of allergen-specific Th2 cell responses induces an IL-2-mediated activation of Tregs with suppressive properties.