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TCRBV20S1 polymorphism does not influence the susceptibility to type 1 diabetes and multiple sclerosis in the

Claudio Fozza1, Magdalena Zoledzieska, Maristella Pitzalis

  • 1Istituto di Ematologia, Universà di Sassari, Viale San Pietro 12, 07100 Sassari, Italy. cfozza@uniss.it

Immunogenetics
|September 20, 2011
PubMed

Among the different T-cell receptor (TCR) BV20S1 polymorphisms, nucleotide substitution at position 524 results in the introduction of a stop codon, whose potential functional relevance is still unknown. We have recently showed in Sardinian subjects the most elevated allele frequency ever reported worldwide for this "null allele" (0.44). As this variant generates a gap in the TCR repertoire, this preliminary finding prompted us to further analyze the role of this polymorphism in the susceptibility to type 1 diabetes (T1D) and multiple sclerosis (MS), which are extremely common in this population. With this aim, we evaluated the influence of the TCRBV20S1 polymorphism by assessing it with the transmission disequilibirum test (TDT) in 652 T1D and 616 MS families, without detecting any significant difference. We conclude that the high frequency of this null allele in Sardinia is not directly related to the high incidence of these autoimmune diseases observed in this founder population.

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