IgE receptor signaling in food allergy pathogenesis

HC Oettgen, OT Burton - Current opinion in immunology, 2015 - Elsevier
HC Oettgen, OT Burton
Current opinion in immunology, 2015Elsevier
Highlights•IgE, IgE receptor signaling and mast cells promote sensitization to food
allergens.•IgE and mast cells disrupt Treg induction, favoring Th2 responses.•Treg that are
generated exhibit Th2 reprogramming and are defective.•Silencing the IgE: mast cell axis
reverses allergic sensitization.The pathogenesis of food allergy remains poorly understood.
Recent advances in the use of murine models have led to discoveries that mast cells and
IgE receptor signaling not only drive immediate hypersensitivity reactions but also exert an …
Highlights
  • IgE, IgE receptor signaling and mast cells promote sensitization to food allergens.
  • IgE and mast cells disrupt Treg induction, favoring Th2 responses.
  • Treg that are generated exhibit Th2 reprogramming and are defective.
  • Silencing the IgE: mast cell axis reverses allergic sensitization.
The pathogenesis of food allergy remains poorly understood. Recent advances in the use of murine models have led to discoveries that mast cells and IgE receptor signaling not only drive immediate hypersensitivity reactions but also exert an immunoregulatory function, promoting the development of allergic sensitivity to foods. We review the evidence that IgE, IgE receptors, key signaling kinases and mast cells impair oral tolerance to ingested foods, preventing the induction of regulatory T cells (Treg) and promoting the acquisition of pro-allergic T helper (Th) 2 responses. We discuss innovative strategies that that could be implemented to counteract these immunoregulatory effects of IgE-mediated mast cell activation, and potentially reverse established sensitization, curing food allergy.
Elsevier