Exp Clin Endocrinol Diabetes 2014; 122(2): 65-70
DOI: 10.1055/s-0033-1363233
Article
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Circulating CD3+56+ Cell Subset in Pre-diabetes

M. Dworacka
1   Department of Pharmacology Poznan University of Medical Sciences, Poznań, Poland
,
A. Wesołowska
1   Department of Pharmacology Poznan University of Medical Sciences, Poznań, Poland
,
E. Wysocka
2   Department of Chemistry and Clinical Biochemistry Poznan University of Medical Sciences, Poznań, Poland
,
H. Winiarska
1   Department of Pharmacology Poznan University of Medical Sciences, Poznań, Poland
,
S. Iskakova
3   Department of Pharmacology, West Kazakhstan State Medical University, Aktobe, Kazakhstan
,
G. Dworacki
4   Department of Clinical Immunology Poznan University of Medical ­Sciences, Poznań, Poland
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 07. August 2013
first decision 15. November 2013

accepted 27. November 2013

Publikationsdatum:
19. Februar 2014 (online)

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Abstract

Background:

The CD3+56+ cells are a small but significant population of T lymphocytes encompassing NKT-like and NKT cells, which may play the essential role at the very early stages of atherosclerotic plaque development. The frequency and activity of CD3+56+ cells in atherosclerosis-inducing dysglycaemic disease (diabetes type 2 or pre-diabetes) is largely unknown.

Methods:

We analysed CD3+56+ cell count, granzyme, perforin and annexin V profiles in the peripheral blood from a group of patients with pre-diabetes, with diabetes type 2 and from non-dysglycaemic controls. Measurements were made of fasting glucose levels, HbA1c, 1,5-anhydroglucitol and lipid profile.

Results:

The mean counts of CD3+56+ cells were significantly higher in patients with pre-diabetes compared to both patients with diabetes and to control group. There was an increase in the number of CD3+56+ cells producing granzyme and perforin in pre-diabetic patients compared to other groups, while there were no difference in annexin V+ populations within examined groups. It was confirmed that CD3+56+ cells count is modified by metabolic factors and their parameters, namely HbA1c and 1,5-anhydroglucitol values.

Conclusion:

It could be stated that the alterations of CD3+ 56+  cells count in peripheral blood of pre-diabetic and type 2 diabetic patients are related to different grades of carbohydrate deteriorations – postprandial hyperglycaemia and chronic hyperglycaemia.