Abstract

Food can trigger a diverse array of symptoms in food allergic individuals from isolated local symptoms affecting skin or gut to multi-system severe reactions (systemic anaphylaxis). Although we know that gastrointestinal and systemic manifestations of food allergy are mediated by tissue mast cells (MCs), it is not clear why allergen exposure by the oral route can result in such distinct clinical manifestations. Our aim was to assess the contribution of mast cell subsets to different manifestations of food allergy. We used two common models of IgE-mediated food allergy, one resulting in systemic anaphylaxis and the other resulting in acute gastrointestinal symptoms, to study the immune basis of allergic reactions. We used responders and non-responders in each model system, as well as naïve controls to identify the association of mast cell activation with clinical reactivity rather than sensitization. Systemic anaphylaxis was uniquely associated with activation of connective tissue mast cells (identified by release of mouse mast cell protease (MMCP) -7 into the serum) and release of histamine, while activation of mucosal mast cells (identified by release of MMCP-1 in the serum) did not correlate with symptoms. Gastrointestinal manifestations of food allergy were associated with an increase of MMCP-1-expressing mast cells in the intestine, and evidence of both mucosal and connective tissue mast cell activation. The data presented in this paper demonstrates that mast cell heterogeneity is an important contributor to manifestations of food allergy, and identifies the connective tissue mast cell subset as key in the development of severe systemic anaphylaxis.

Highlights

  • Mast cells (MCs) are the main effector cells in IgE-mediated food allergy [1], but the understanding of their role is incomplete

  • Of the vast number of bioactive molecules that are produced by MCs, histamine and platelet activating factor (PAF) contribute to peanut-induced systemic anaphylaxis in mice and humans [4,5,6], while serotonin and PAF are the main mediators that contribute to gastrointestinal symptoms in mice [7]

  • Systemic anaphylaxis together with gastrointestinal symptoms has been reported in Balb/c mice after oral challenge [17, 18], we did not record any drop in body temperature in epicutaneously sensitized Balb/c mice with diarrhea symptoms

Read more

Summary

Introduction

Mast cells (MCs) are the main effector cells in IgE-mediated food allergy [1], but the understanding of their role is incomplete. Symptoms triggered by foods occur within 2 hours of ingestion, and can affect single or multiple organ systems, including the skin (hives), the respiratory tract (bronchoconstriction, cough), and the gastrointestinal tract (nausea, vomiting, diarrhea) [2]. Mast cell heterogeneity and food allergy mucosal symptoms [3]. Of the vast number of bioactive molecules that are produced by MCs, histamine and platelet activating factor (PAF) contribute to peanut-induced systemic anaphylaxis in mice and humans [4,5,6], while serotonin and PAF are the main mediators that contribute to gastrointestinal symptoms in mice [7]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call