Avtor/Urednik     Tomažič, J; Ihan, A
Naslov     Flow cytometric analysis of lymphocytes in cerebrospinal fluid in patients with tick-borne encephalitis
Tip     članek
Vir     Acta Neurol Scand
Vol. in št.     Letnik 95, št. 1
Leto izdaje     1997
Obseg     str. 29-33
Jezik     eng
Abstrakt     INTRODUCTION: Cerebrospinal fluid (CSF) lymphocyte subsets were examined by flow cytometry in 33 patients with tick-borne encephalitis (TBE) in order to determine their values. PATIENTS AND METHODS: Lymphocytes were isolated from CSF and lymphocyte subsets were determined: lymphocytes T (CD3+), lymphocytes B (CD19+), NK cells (CD3-CD56+), helper T cells (CD3+CD4+) and cytotoxic T cells (CD3+CD8+). The expression of IL-2 receptors (CD25+) and transferrin receptors (CD71+) on T cells and HLA-DR molecules on T cell subsets was examined. Furthermore, possible relationships among different TBE patient population variables (gender, age, severity of disease, duration of meningitis) were considered. RESULTS: The analyses of the CSF lymphocyte population subsets are presented. Lymphocytes T (CD3+) were significantly higher in the CSF than in the peripheral blood as was the case with the T cells that expressed transferrin receptors (CD71). Lymphocytes B (CD19+) and NK cells (CD3-CD56+) prevailed in the peripheral blood. In the early course of the disease, a higher expression of HLA-DR molecules on T lymphocytes was observed, while later a higher expression of IL-2 receptors (CD25+) was observed. DISCUSSION: Significant differences in lymphocyte subsets between the CSF and the peripheral blood were found. Significant time-dependent changes of CSF lymphocyte subsets during course of infection were observed. The results of the present study give us deeper insight into CNS cellular immunopathogenic mechanisms in patients with TBE.
Deskriptorji     CELL SEPARATION
CEREBROSPINAL FLUID
ENCEPHALITIS, TICK-BORNE
FLOW CYTOMETRY
T-LYMPHOCYTES
ADULT
ANTIBODIES, MONOCLONAL
B-LYMPHOCYTES
ENZYME-LINKED IMMUNOSORBENT ASSAY
HLA-DR ANTIGENS
IGG
IGM
KILLER CELLS, NATURAL