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Immune Regulatory T Cells in Siblings of Children Suffering from Type 1 Diabetes Mellitus.
- Source :
- Scandinavian Journal of Immunology; Nov2006, Vol. 64 Issue 5, p531-535, 5p, 1 Chart, 4 Graphs
- Publication Year :
- 2006
-
Abstract
- Patients with type 1 diabetes are suffering from defects in immune regulatory cells. Their siblings may be at increased risk of type 1 diabetes especially if they are carriers of certain human leucocyte antigen (HLA) alleles. In a prospective non-randomized study, we intended to evaluate 31 healthy siblings of paediatric patients with type 1 diabetes and explore immune regulatory populations of CD4<superscript>+</superscript>CD25<superscript>+</superscript> T cells and natural killer (NK) T cells. Tested siblings of type 1 diabetes patients were stratified according to the HLA-associated risk of possible diabetes development. Immune regulatory function of CD4<superscript>+</superscript>CD25<superscript>+</superscript> T cells was tested in vitro. Significant differences in CD4<superscript>+</superscript>CD25<superscript>+</superscript> but not in NK T cells have been identified. Siblings of type 1 diabetes patients carrying high risk HLA alleles (DQA1*05, DQB1*0201, DQB1*0302) had significantly lower number of immune regulatory CD4<superscript>+</superscript>CD25<superscript>+</superscript> T cells than the age-matched healthy controls or siblings carrying low-risk HLA alleles (DQB1*0301, DQB1*0603, DQB1*0602). Regulatory function of CD4<superscript>+</superscript>CD25<superscript>+</superscript> T cells demonstrated a dose-escalation effect. In siblings of type 1 diabetes patients, the defect in immune regulatory CD4<superscript>+</superscript>CD25<superscript>+</superscript> T cells exists in association with genetic HLA-linked risk for type 1 diabetes. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03009475
- Volume :
- 64
- Issue :
- 5
- Database :
- Complementary Index
- Journal :
- Scandinavian Journal of Immunology
- Publication Type :
- Academic Journal
- Accession number :
- 22615332
- Full Text :
- https://doi.org/10.1111/j.1365-3083.2006.01837.x