HLA-DO polymorphism associated with resistance to type I diabetes detected with monoclonal antibodies, isoelectric point differences, and restriction fragment length polymorphism

نویسندگان

  • G M Schreuder
  • M G Tilanus
  • R E Bontrop
  • G J Bruining
  • M J Giphart
  • J J van Rood
  • R R de Vries
چکیده

A new HLA-DQ-related genetic system with two alleles, 2B3 and TA10, defined serologically by MAbs and alloantisera, showed an almost perfect correlation with charge differences on DQ beta molecules, as well as with two polymorphic DNA fragments hybridizing with a DQ beta probe and various restriction enzymes on a panel of 14 DR4+ homozygous typing cells. It was therefore concluded that the serologically defined alleles 2B3 and TA10 are coded by the DQ beta gene and situated on the HLA-DQ beta chain. This 2B3/TA10 polymorphism is independent of HLA-D and segregates with HLA in families. The TA10 allele appears to be a new marker for resistance to type I diabetes, which is independent from the known resistance marker DR2, whereas no association was observed between this DQ beta polymorphism and rheumatoid arthritis.

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BriefDefinitive Report HLA-DQ POLYMORPHISM ASSOCIATED WITH RESISTANCE TO TYPE I DIABETES DETECTED WITH MONOCLONAL ANTIBODIES, ISOELECTRIC POINT DIFFERENCES, AND RESTRICTION FRAGMENT LENGTH POLYMORPHISM

Recently (1), we described a new genetic system that is HLA-DQ-related . Two alleles, 2B3 and TA10, can be recognized serologically . The 2133 specificity detected with the 11133 mAb was previously described (2) as a DQwl-related specificity . The TA 10 specificity is DQw3-related and was first. described by Maeda (3) with the TA 10 mAb. TA10 can also be detected with alloantisera (4) . Recentl...

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عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 164  شماره 

صفحات  -

تاریخ انتشار 1986