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.

Evaluation of T-cell receptor CD3(+) gamma delta in gestational diabetes mellitus

LAPOLLA, ANNUNZIATA;BETTERLE, CORRADO;PLEBANI, MARIO;FEDELE, DOMENICO
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.
2000
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2470824
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