Distinct transcriptome profiles differentiate nonsteroidal anti-inflammatory drug-dependent from nonsteroidal anti-inflammatory drug-independent food-induced anaphylaxis

J Allergy Clin Immunol. 2016 Jan;137(1):137-146. doi: 10.1016/j.jaci.2015.05.042. Epub 2015 Jul 17.

Abstract

Background: Lipid transfer protein (LTP), an abundant protein in fruits, vegetables, and nuts, is a common food allergen in Mediterranean areas causing diverse allergic reactions. Approximately 40% of food-related anaphylaxis induced by LTPs requires nonsteroidal anti-inflammatory drugs (NSAIDs) as a triggering cofactor.

Objective: We sought to better understand the determinants of NSAID-dependent and NSAID-independent LTP-induced anaphylaxis (LTP-A).

Methods: Selection of patients was based on a proved clinical history of NSAID-dependent or NSAID-independent anaphylaxis to LTPs, positive skin prick test response to LTPs, and serum LTP IgE. Whole-transcriptome (RNA sequencing) analysis of blood cells from 14 patients with NSAID-related LTP-A (NSAID-LTP-A), 7 patients with LTP-A, and 13 healthy control subjects was performed to identify distinct gene expression signatures.

Results: Expression of genes regulating gastrointestinal epithelial renewal was altered in both patient sets, particularly in those with LTP-A, who also presented with gene expression profiles characteristic of an inflammatory syndrome. These included altered B-cell pathways, increased neutrophil activation markers, and increased reactive oxygen species levels. Increased expression of the IgG receptor (CD64) in patients with LTP-A was mirrored by the presence of LTP-specific IgG1 and IgG3. Conversely, patients with NSAID-LTP-A were characterized by reduced expression of IFN-γ-regulated genes and IFN-γ levels, as well as upregulated expression of adenosine receptor 3 (ADORA3) and genes related to adenosine metabolism.

Conclusions: Gene ontology analysis suggests disturbances in gut epithelial homeostasis in both groups with LTP-A, with potential integrity breaches in patients with LTP-A that might explain their distinct inflammatory signatures. Differential regulation in patients with LTP-A and those with NSAID-LTP-A of the IFN-γ pathway, IgG receptors, and ADORA3 might provide the pathogenic basis of their distinct responses.

Keywords: Anaphylaxis; food allergy; lipid transfer protein syndrome; nonsteroidal anti-inflammatory drugs; transcriptome analysis.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allergens / immunology*
  • Anaphylaxis / genetics*
  • Anaphylaxis / immunology
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
  • Carrier Proteins / immunology*
  • Female
  • Food Hypersensitivity / genetics*
  • Food Hypersensitivity / immunology
  • Humans
  • Immunoglobulin G / immunology
  • Interferon-gamma / immunology
  • Male
  • Middle Aged
  • Receptor, Adenosine A3 / genetics
  • Receptors, IgG / genetics
  • Sequence Analysis, RNA
  • Transcriptome*

Substances

  • Allergens
  • Anti-Inflammatory Agents, Non-Steroidal
  • Carrier Proteins
  • FCGR1A protein, human
  • Immunoglobulin G
  • Receptor, Adenosine A3
  • Receptors, IgG
  • lipid transfer protein
  • Interferon-gamma