Optimal strategies to identify aberrant intra-epithelial lymphocytes in refractory coeliac disease

J Clin Immunol. 2014 Oct;34(7):828-35. doi: 10.1007/s10875-014-0075-7. Epub 2014 Jul 27.

Abstract

Introduction: Different strategies have been developed to identify those refractory celiac disease (RCD) patients who are at risk to develop an enteropathy associated T-cell lymphoma (EATL). Flow cytometric analysis of intra-epithelial lymphocytes (IEL) with an aberrant phenotype is considered the golden standard but is not widely available. Immunohistochemistry (IHC) and T-cell receptor (TCR) rearrangement studies are commonly available but may lack sensitivity and specificity. Here, we compared the three different methods in the workup of patients suspected for RCD.

Methods: Duodenal biopsies from control patient (n = 5), RCD patients with moderately increased aberrant IEL populations (20-50 %: n = 14), and RCD patients with high numbers of aberrant IEL (>50 %: n = 5) as determined by flow cytometry were analysed by IHC and TCR-γ chain rearrangement analysis. Three pathologists scored the slides independently.

Results: Sensitivity of IHC and TCR-γ rearrangement analysis in RCD patients with high numbers of aberrant IELs was 100 and 71 %, respectively. RCD patients with aberrant cells between 25 and 50 % however, were missed by IHC and TCR in 50 and 57 % of cases, respectively. In addition, inter-rater reliability analysis of the IHC scoring revealed coder-pair Kappa coefficients between 0.28 and 0.85.

Conclusion: Immunohistochemistry and to a lesser extent TCR-γ clonality analysis are sensitive in identifying patients with high numbers of aberrant IEL populations, yet miss half of RCD patients with moderately increased numbers. In addition, IHC has a high inter-observer variability. Therefore, patients suspected for RCD should undergo flow cytometric analysis of the duodenum.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • CD4-Positive T-Lymphocytes / immunology*
  • Celiac Disease / complications
  • Celiac Disease / diagnosis*
  • Celiac Disease / immunology
  • Cell Separation / methods
  • Drug Resistance
  • Female
  • Flow Cytometry
  • Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor / genetics
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / pathology
  • Lymphoma, T-Cell / diagnosis*
  • Lymphoma, T-Cell / etiology
  • Lymphoma, T-Cell / immunology
  • Male
  • Middle Aged
  • Observer Variation
  • Receptors, Antigen, T-Cell / genetics
  • Recurrence
  • Sensitivity and Specificity
  • Young Adult

Substances

  • Receptors, Antigen, T-Cell