Deep sequencing of blood and gut T-cell receptor β-chains reveals gluten-induced immune signatures in celiac disease.

Interestingly, compared to the private DA clonotypes of each patient, higher rate of convergent selection (multiple nucleotide clonotypes coding for identical amino acid clonotype) appears to be a feature of these ‘public subset’ of the DA clonotypes with an increasing trend during gluten exposure (Supplementary Figure S10 ).

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