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The Journal of Experimental Medicine· 2012Q1

Wheat amylase trypsin inhibitors drive intestinal inflammation via activation of toll-like receptor 4

Yvonne Junker, Sebastian Zeißig, Seong‐Jun Kim, Donatella Barisani et al.

Short summary

Wheat amylase trypsin inhibitors (ATIs) activate innate immune responses via TLR4, driving intestinal inflammation in celiac disease and potentially other immune disorders.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Wheat ATIs activate innate immune cells (monocytes, macrophages, dendritic cells) via the TLR4-MD2-CD14 complex.
  • ATI activation leads to increased maturation markers and pro-inflammatory cytokine release.
  • Both celiac and non-celiac patients' cells respond to ATIs.
  • Mice deficient in TLR4 signaling are protected from ATI-induced immune responses.
  • ATIs are identified as novel contributors to celiac disease and potentially other immune disorders.

AI-generated from the title and abstract; the full text is not read.

Abstract

Ingestion of wheat, barley, or rye triggers small intestinal inflammation in patients with celiac disease. Specifically, the storage proteins of these cereals (gluten) elicit an adaptive Th1-mediated immune response in individuals carrying HLA-DQ2 or HLA-DQ8 as major genetic predisposition. This well-defined role of adaptive immunity contrasts with an ill-defined component of innate immunity in celiac disease. We identify the α-amylase/trypsin inhibitors (ATIs) CM3 and 0.19, pest resistance molecules in wheat, as strong activators of innate immune responses in monocytes, macrophages, and dendritic cells. ATIs engage the TLR4-MD2-CD14 complex and lead to up-regulation of maturation markers and elicit release of proinflammatory cytokines in cells from celiac and nonceliac patients and in celiac patients' biopsies. Mice deficient in TLR4 or TLR4 signaling are protected from intestinal and systemic immune responses upon oral challenge with ATIs. These findings define cereal ATIs as novel contributors to celiac disease. Moreover, ATIs may fuel inflammation and immune reactions in other intestinal and nonintestinal immune disorders.

The authors' abstract, as published at the source. The Journal of Experimental Medicine, 2012 · DOI ↗

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Field: Gastroenterology

GastroenterologyMedicine