Abstract

Symptom occurrence at the first ingestion suggests that food allergy may result from earlier sensitization via non-oral routes. We aimed to characterize the cellular populations recruited at various mucosal and immune sites after experimental sensitization though different routes. BALB/cJ mice were exposed to a major allergenic food (peanut) mixed with cholera toxin via the intra-gastric (i.g.), respiratory, cutaneous, or intra-peritoneal (i.p.) route. We assessed sensitization and elicitation of the allergic reaction and frequencies of T cells, innate lymphoid cells (ILC), and inflammatory and dendritic cells (DC) in broncho-alveolar lavages (BAL), lungs, skin, intestine, and various lymph nodes. All cellular data were analyzed through non-supervised and supervised uni/multivariate analysis. All exposure routes, except cutaneous, induced sensitization, but intestinal allergy was induced only in i.g.- and i.p.-exposed mice. Multivariate analysis of all cellular constituents did not discriminate i.g. from control mice. Conversely, respiratory-sensitized mice constituted a distinct cluster, characterized by high local inflammation and immune cells recruitment. Those mice also evidenced changes in ILC frequencies at distant site (intestine). Despite absence of sensitization, cutaneous-exposed mice evidenced comparable changes, albeit less intense. Our study highlights that the initial route of sensitization to a food allergen influences the nature of the immune responses at various mucosal sites. Interconnections of mucosal immune systems may participate in the complexity of clinical manifestations as well as in the atopic march.

Highlights

  • Food allergy (FA) is an inappropriate immune reaction to food proteins that mainly involves production of specific IgE [1]

  • In genetically predisposed individuals, and due to specificenvironmental signals, naïve CD4+ T lymphocytes can differentiate into Type 2 helper cells (Th2) that produce cytokines such as IL-4/5/13 and that will in turn induce production of specific IgE by B lymphocytes

  • protein extract (PE) and oral food challenge (OFC) solutions were characterized by assessment of total protein concentrations (PierceTM BCA protein assay kit, Thermo ScientificTM, Waltham, MA, USA, following the manufacturer’s instructions) and by electrophoresis to ensure the presence of the major peanut allergens [10,11]

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Summary

Introduction

Food allergy (FA) is an inappropriate immune reaction to food proteins that mainly involves production of specific IgE (type E immunoglobulins) [1]. In genetically predisposed (i.e., atopic) individuals, and due to specific (micro)environmental signals, naïve CD4+ T lymphocytes can differentiate into Type 2 helper cells (Th2) that produce cytokines such as IL-4/5/13 and that will in turn induce production of specific IgE by B lymphocytes. These IgE circulate throughout the body and bind to mucosal mast cells [2]

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