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Interleukin 18 and associated markers of T helper cell type 1 activity in coeliac disease
  1. V M Salvati1,
  2. T T MacDonald2,
  3. M Bajaj-Elliott3,
  4. M Borrelli1,
  5. A Staiano1,
  6. S Auricchio1,
  7. R Troncone1,
  8. G Monteleone2
  1. 1Department of Pediatrics and European Laboratory for the Investigation of Food-Induced Diseases, University Federico II, Naples, Italy
  2. 2Division for Infection, Inflammation, and Repair, University of Southampton, Southampton, UK
  3. 3Department of Paediatric and Adult Gastroenterology, St Bartholomews and the Royal London School of Medicine and Dentistry, London, UK
  1. Correspondence to:
    G Monteleone, Division of Infection, Inflammation, and Repair, School of Medicine, Southampton General Hospital, MailPoint 813, Level E, South Academic Block, Tremona Road, Southampton SO16 6YD, UK;
    g.monteleone{at}soton.ac.uk

Abstract

Background: Coeliac disease (CD) is caused by a T helper cell type 1 (Th1) response in the small intestinal mucosa to dietary gluten. Paradoxically, interleukin (IL)-12, the major Th1 inducing factor, is undetectable in the mucosa of active CD. IL-18 is a recently described cytokine capable of promoting T cell interferon (IFN)-γ production and facilitating Th1 cell polarisation.

Aim: To examine expression of IL-18 and IL-18-associated Th1 proteins in CD.

Methods: IL-18 and IFN-γ RNA transcripts were determined by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). IL-18 and caspase-1 protein expression were assessed by western blotting. Caspase-1 activity was determined using a commercially available assay. RNA transcripts for the IL-18 receptor subunits, IL-1 receptor related protein (IL-1 Rrp) and accessory protein-like subunit (AcPL), and IL-18 induced Th1 specific T box transcription factor (T-bet) were measured by RT-PCR and Southern blotting.

Results: IL-18 RNA transcripts were found in all mucosal samples analysed, with no difference between CD patients and controls. By western blot analysis, a large protein of approximately 24 kDa, corresponding to the immature IL-18, was detected in all mucosal samples from CD patients and controls. In contrast, mature IL-18 was only seen in CD patients. Immunoreactivity corresponding to both immature and mature caspase-1 was present in both CD and control samples. Tissue homogenates from CD patients and controls expressed similar levels of caspase-1 activity. IL-1Rrp and AcPL were seen in all samples but were expressed at greater levels in the mucosa of CD patients. T-bet was also upregulated in CD.

Conclusions: Active IL-18 is expressed in CD as well as other markers of Th1 polarisation.

  • coeliac disease
  • interleukin 18
  • Th1 response
  • CD, coeliac disease
  • IFN, interferon
  • IL, interleukin
  • T-bet, T box transcription factor
  • IL-1Rrp, interleukin 1 receptor related protein
  • AcPL, accessory protein-like
  • RT-PCR, reverse transcriptase-polymerase chain reaction
  • ICE, IL-1β converting enzyme
  • Th1, T helper cell type 1

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