Anti-transglutaminase immunoreactivity and histological lesions of the duodenum in coeliac patients

Int Immunol. 2013 Jun;25(6):389-94. doi: 10.1093/intimm/dxs159. Epub 2013 Feb 26.

Abstract

Coeliac disease (CD) is characterized by several markers, including anti-transglutaminase auto-antibodies (tTGAb) directed against multiple epitopes of the gliadin protein. We aimed to investigate the correlation among CD duodenal lesions, tTGAb titres and the immunoreactivity against tTG constructs. A total of 345 CD patients (209 females, 136 males, overall median age: 7.3 years) were tested for full-length (fl) tTGAb with a fluid-phase radioimmunoassay. Out of the total, 231 patients were also tested for immunoreactivity against tTG fragments (F1: a.a. 227-687 and F2: a.a. 473-687). Patients were classified according to diffuse (D), patchy (P) or bulb (B) histological lesions. All sera were found fltTGAb positive. Patients with D, P and B lesions had a mean Ab index of 0.84±0.39, 0.57±0.39 and 0.45±0.24, respectively. Mean tTGAb titre varied between D and localized (P+B) patients (0.84±0.39 versus 0.52±0.34, P < 0.0001). Overall, 86.1% of patients were F1 auto-antibody (F1Ab) positive (D: 89%, P: 75%, B: 40%; D versus P+B: P = 0.004) and 49% of patients were F2 auto-antibody (F2Ab) positive (D: 53%, P: 19%, B: 10%; D versus P+B: P = 0.0006). Of the D patients 50.7% showed combined F1Ab-F2Ab (D versus P+B: P = 0.001), whereas 60% of B patients were negative for both F1Ab and F2Ab (B versus D: P < 0.0001). Coeliac-specific tTGAb immunoreactivity correlates with the grading and extension of histological duodenal lesions in CD patients at diagnosis. The immunoreactivity against single and combined tTG fragments is significantly higher in patients with D lesions. This is the first evidence of a distinct coeliac-specific immunoreactivity in patients with different duodenal involvement.

Keywords: anti-transglutaminase antibodies; coeliac disease; histological lesions; tTG target domains.

MeSH terms

  • Adolescent
  • Adult
  • Celiac Disease / enzymology
  • Celiac Disease / immunology*
  • Celiac Disease / pathology*
  • Child
  • Child, Preschool
  • Duodenum / enzymology
  • Duodenum / immunology*
  • Duodenum / pathology*
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Retrospective Studies
  • Transglutaminases / immunology*
  • Young Adult

Substances

  • Transglutaminases