CD 127- and FoxP3+ expression on CD25+CD4+ T regulatory cells upon specific diabetogeneic stimulation in high-risk relatives of type 1 diabetes mellitus patients
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18248531
DOI
10.1111/j.1365-3083.2008.02074.x
PII: SJI2074
Knihovny.cz E-zdroje
- MeSH
- antigeny CD4 analýza MeSH
- diabetes mellitus 1. typu imunologie MeSH
- dospělí MeSH
- forkhead transkripční faktory analýza MeSH
- kultivované buňky MeSH
- lidé MeSH
- mladiství MeSH
- počet lymfocytů MeSH
- průtoková cytometrie MeSH
- receptor interleukinu-2 - alfa-podjednotka analýza MeSH
- receptor interleukinu-7 - alfa-podjednotka analýza MeSH
- regulační T-lymfocyty imunologie MeSH
- rizikové faktory MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD4 MeSH
- forkhead transkripční faktory MeSH
- FOXP3 protein, human MeSH Prohlížeč
- receptor interleukinu-2 - alfa-podjednotka MeSH
- receptor interleukinu-7 - alfa-podjednotka MeSH
Abnormalities in CD4+CD25+ regulatory T cells (Treg) may contribute to type 1 diabetes (T1D) development. First-degree relatives of T1D patients are at increased risk especially when they carry certain HLA II haplotypes. Using two novel markers of CD4+CD25+ Treg (CD127- and FoxP3+ respectively), we evaluated number and function of Treg after specific stimulation with diabetogeneic autoantigens in 11 high-risk (according to HLA-linked risk) relatives of T1D patients and 14 age-matched healthy controls using a cytokine secretion assay based on interferon-gamma (IFN-gamma) production. High-risk relatives of T1D patients had significantly lower pre- and post-stimulatory number of CD127- Treg than that of healthy controls (P < 0.05). Labelling Treg with FoxP3+ demonstrated similar trend but did not reach statistical significance. Although the stimulation with diabetogenic autoantigens did not lead to a significant change in number of Treg in both groups, the defective function of Treg was performed by significantly higher activation of diabetogeneic T cells in high-risk relatives of T1D patients compared to healthy controls (P < or = 0.02). Individuals at increased HLA-associated genetic risk for T1D showed defects in Treg.
Citace poskytuje Crossref.org
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