Coeliac disease

Aberrant extrathymic T cell receptor gene rearrangement in the small intestinal mucosa: a risk factor for coeliac disease?

A Bas¹, G Forsberg^1,2, V Sjöberg¹, S Hammarström¹, O Hernell², M-L Hammarström¹

¹ Department of Clinical Microbiology, Immunology, Umeå University, Umeå, Sweden
² Department of Clinical Sciences, Pediatrics, Umeå University, Umeå, Sweden

Dr M-L Hammarström, Umeå University, Immunology, SE-90185 Umeå, Sweden; Marie-Louise.Hammarstrom{at}climi.umu.se

Background: Coeliac disease is a small intestine enteropathy caused by permanent intolerance to wheat gluten. Gluten intake by patients with coeliac disease provokes a strong reaction by intestinal intraepithelial lymphocytes (IELs), which normalises on a gluten-free diet.

Aim: To investigate whether impaired extrathymic T cell maturation and/or secondary T cell receptor (TCR) gene recombination in IELs are features of coeliac disease which could contribute to the failure of establishing tolerance to gluten.

Methods: Expression levels of the four splice-forms of recombination activating gene-1 (RAG1) mRNA and preT -chain (preT) mRNA were determined in IEL-subsets of children with coeliac disease and controls. Frequencies of RAG1 expressing IELs were determined by immunomorphometry.

Results: In controls, the RAG1-1A/2 splice-form selectively expressed outside the thymus, was dominant and expressed in both mature (TCR⁺) and immature (CD2⁺CD7⁺TCR^–) IELs (8 mRNA copies/18S rRNA U). PreT was expressed almost exclusively in CD2⁺CD7⁺TCR^– IELs (40 mRNA copies/18S rRNA U). By contrast, RAG1 and preT mRNA levels were low in patients with coeliac disease compared to controls, both with active disease and with inactive, symptom-free disease on a gluten-free diet (p values <0.01 for mature and <0.05 for immature IELs). Similarly, the frequencies of RAG1+ IELs were significantly lower in patients with coeliac disease compared to controls (p<0.001).

Conclusions: Patients with coeliac disease appear to have an impaired capacity for extrathymic TCR gene rearrangement. This is an inherent feature, which probably plays a pivotal role in the failure to efficiently downregulate the T cell response to gluten.

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