Publication Date:
2000
abstract:
Few studies have shown a significant increase of CD3+ T-cell receptor (TCR) γδ in the early phases of type 1 diabetes. We wished to determine if CD3+ TCR γδ is involved in the pathogenesis of gestational diabetes mellitus (GDM). We studied 29 GDM patients and 21 normal pregnant women. Lymphocyte subpopulations (CD3+ TCR αβ, CD3+ TCR γδ), islet cell antibodies (ICA), glutamic acid decarboxylase antibodies (GAD) and protein tyrosine phosphatase antibodies (IA2-Ab) were evaluated in all patients. The percentage of CD3+ TCR γδ was significantly higher in GDM women than in the control group (5.1 ± 2.9% vs 3.7 ± 1.7%; p < 0.05). No abnormalities of the other lymphocyte subpopulations were found. All subjects were negative for ICA; 2 GDM patients were positive for GAD, but no relationship was found between GAD positivity and CD3+ γδ levels in these 2 patients. Further follow-up studies of these patients are required to verify if the CD3+ TCR γδ receptor is a useful marker for diabetes development.
Iris type:
01.01 - Articolo in rivista
Keywords:
Autoimmunity; CD3; +; γδ lymphocytes; Gestational diabetes mellitus;
List of contributors:
Lapolla, Annunziata; Sanzari, M; Betterle, Corrado; Dalfrà, Mg; Masin, M; Zanchetta, R; Zancanaro, F; Capovilla, F; Toniato, R; Plebani, Mario; Fedele, Domenico
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