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Excess of maternal HLA-DR3 antigens in HLA DR3,4 positive type 1 (insulin-dependent) diabetic patients
I Deschamps1, J Hors, F Clerget-Darpoux
1INSERM U.30, Hôpital des Enfants Malades, Paris, France.
Insights
Parental origin of HLA-DR3 and HLA-DR4 influences Type 1 diabetes risk. Maternal DR3 combined with paternal DR4 increases disease susceptibility in siblings, suggesting a role in pathogenesis.
Area of Science:
- Immunogenetics
- Endocrinology
- Human Genetics
Background:
- Type 1 diabetes susceptibility is linked to HLA-DR3 and HLA-DR4.
- The influence of parental origin of these HLA antigens on disease susceptibility is not well understood.
Purpose of the Study:
- To investigate whether the parental origin of HLA-DR3 and HLA-DR4 haplotypes affects susceptibility to Type 1 diabetes.
Main Methods:
- Analysis of HLA-DR3 and HLA-DR4 haplotype inheritance from parents in 246 simplex and 41 multiplex diabetic families.
- Study included affected and unaffected siblings, and an additional 80 multiplex families (GAW 5).
Main Results:
- A non-random distribution of paternal and maternal DR3 and DR4 antigens was observed in affected individuals.
- Individuals with DR4 from their father and DR3 from their mother (DR4p/DR3m) were more common (62-72%) than expected (50%).
- Siblings with DR4p/DR3m showed a significantly higher disease risk compared to those with DR3p/DR4m.
Conclusions:
- Maternal DR3, particularly in conjunction with paternal DR4, may enhance Type 1 diabetes pathogenesis.
- Parental origin of HLA antigens is a significant factor in Type 1 diabetes risk stratification.
Abstract:
The susceptibility determinants of Type 1 (insulin-dependent) diabetes mellitus are known to be associated with both HLA-DR3 and DR4. In our study we wished to determine if the parental origin of these antigens could influence susceptibility to the disease. We analysed the inheritance of DR3 and DR4 haplotypes from the father or mother (DR3p, DR4p, DR3m and DR4m, respectively), in the index cases and in the affected and non-affected siblings of 246 diabetic simplex and 41 multiplex families without affected parents. An independent series of 80 multiplex families (GAW 5) was also studied. Among the DR3,4 positive index cases and affected siblings, the paternal and maternal DR3 and DR4 antigens were not distributed randomly: 62% and 72%, respectively, had received DR4 from their father and DR3 from their mother (DR4p/DR3m), while only 38% and 28%, respectively, had received a paternal DR3 together with a maternal DR4 (DR3p/DR4m). This differed significantly from the 50% expected ratio (p less than 0.01) and was not observed in unaffected siblings. No excess of maternal DR3 in the absence of DR4 and no excess of paternal DR4 in the absence of DR3 were observed. The finding suggests that some maternal DR3 related event (presumably during pregnancy) might play an enhancing role in the pathogenesis of Type 1 diabetes. It also implies that siblings with both DR4p and DR3m have a significantly higher risk for disease than those with DR3p and DR4m.
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