Abstract
Background: Gluten proteins can induce celiac disease (CD) in genetically susceptible individuals.
In CD patients gluten-derived peptides are presented to the immune system, which leads to a
CD4+ T-cell mediated immune response and inflammation of the small intestine. However, not all
gluten proteins contain T-cell stimulatory epitopes. Gluten proteins are encoded by multigene loci
present on chromosomes 1 and 6 of the three different genomes of hexaploid bread wheat
(Triticum aestivum) (AABBDD).
Results: The effects of deleting individual gluten loci on both the level of T-cell stimulatory
epitopes in the gluten proteome and the technological properties of the flour were analyzed using
a set of deletion lines of Triticum aestivum cv. Chinese Spring. The reduction of T-cell stimulatory
epitopes was analyzed using monoclonal antibodies that recognize T-cell epitopes present in gluten
proteins. The deletion lines were technologically tested with respect to dough mixing properties
and dough rheology. The results show that removing the α-gliadin locus from the short arm of
chromosome 6 of the D-genome (6DS) resulted in a significant decrease in the presence of T-cell
stimulatory epitopes but also in a significant loss of technological properties. However, removing
the ω-gliadin, γ-gliadin, and LMW-GS loci from the short arm of chromosome 1 of the D-genome
(1DS) removed T-cell stimulatory epitopes from the proteome while maintaining technological
properties.
Conclusion: The consequences of these data are discussed with regard to reducing the load of Tcell
stimulatory epitopes in wheat, and to contributing to the design of CD-safe wheat varieties.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 1-12 |
| Number of pages | 12 |
| Journal | BMC Plant Biology |
| Volume | 9 |
| Issue number | 41 |
| Publication status | Published - 2009 |