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A new algorithm for coeliac disease based on the 'long forgotten' TCRγδ intra-epithelial lymphocytes detected with an antibody working on FFPE sections. | LitMetric

AI Article Synopsis

  • Researchers aimed to improve the diagnosis of coeliac disease (CD) with mild mucosal changes by using a new monoclonal antibody to study T cell receptor (TCR)γδ intra-epithelial lymphocytes (IELs).
  • They analyzed 167 cases, including untreated CD and non-coeliac groups, and found that TCRγδ IEL levels were significantly higher in CD patients, correlating with mucosal damage severity.
  • The study proposes a diagnostic algorithm based on γδ IEL counts and ratios, which accurately classified most cases and could enhance histopathological diagnosis for coeliac disease.

Article Abstract

Aims: Diagnosis of coeliac disease (CD) with mild mucosal changes is difficult for all parties involved. We aimed to determine the power of T cell receptor (TCR)γδ intra-epithelial lymphocytes (IELs) in discriminating CD from other causes of intra-epithelial lymphocytosis using a new monoclonal antibody.

Methods: A total of 167 cases categorised as coeliac (117 untreated CD, classified according to Marsh, updated by Ensari, including 29 type 1, 29 type 2, 39 type 3 and 20 treated CD), and non-coeliac groups (24 controls and 26 non-coeliac IELosis) based on clinical, serological and histological data were studied for IEL counts enumerated per 100 enterocytes using haematoxylin and eosin, CD3, TCR δ-stains.

Results: TCRγδ IELs were significantly higher in CD (24.83 ± 16.13) compared to non-CD (6.72 ± 6.32) and were correlated with the degree of mucosal damage. Both γδ IEL count and ratio showed higher performance in differentiating untreated coeliacs from controls, with a sensitivity of 83.76; 85.57 and specificity of 95.83; 79.17, respectively. TCRγδ IEL counts distinguished type 1 CD (20.41 ± 13.57) from non-coeliac IELosis (9.42 ± 7.28) (p = 0.025). Discriminant analysis revealed that villus/crypt ratio, γδ and CD3 IEL counts, γδ/CD3IEL ratio, IEL distribution pattern were potent discriminants and correctly classified 82.3% of cases while the algorithm accurately diagnosed 93.4% of cases.

Conclusions: The new antibody detecting γδ IELs in FFPE sections revealed thresholds of 10.5 for γδ IELs and 14% for γδ/CD3IEL ratio which distinguished coeliacs from non-coeliacs with high sensitivity and specificity, particularly in cases with normal villus/crypt axis including type 1 CD, non-CD IELosis and controls. A 'coeliac algorithm' based on γδ IELs is proposed with the hope that it will be used in the histopathological diagnostic approach by the pathology community.

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Source
http://dx.doi.org/10.1111/his.15330DOI Listing

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