Flow cytometry of cerebrospinal fluid (CSF) lymphocytes: Alterations of blood CSF ratios of lymphocyte subsets in inflammation disorders of human central nervous system (CNS)

Citation
To. Kleine et al., Flow cytometry of cerebrospinal fluid (CSF) lymphocytes: Alterations of blood CSF ratios of lymphocyte subsets in inflammation disorders of human central nervous system (CNS), CLIN CH L M, 37(3), 1999, pp. 231-241
Citations number
56
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
ISSN journal
14346621 → ACNP
Volume
37
Issue
3
Year of publication
1999
Pages
231 - 241
Database
ISI
SICI code
1434-6621(199903)37:3<231:FCOCF(>2.0.ZU;2-1
Abstract
Flow cytometry was adapted to measure lymphocytes in human cerebrospinal fl uid (CSF). The method was sufficiently precise, reproducible and accurate d espite low cell counts. In lumbar CSF of controls with 500 to 3500 (10(3)/I ) leukocytes, lymphocyte counts correlated with those in corresponding veno us blood: blood/CSF ratios of approximate to 2000 : 1 were found for total T cells (CD3(+)) and CD3(+) HLA-DR-, CD3(+)4(+), CD3(+)8(+) subsets, ratios were increased for the lymphocyte subsets CD3(+) HLA-DR+ less than or equa l to; CD3(+)16(+)56(+) < CD16(+)56(+)3(-) < CD8(+)3(-) much less than CD19( +); CD8(+)4(+) ratio was half of CD3(+) ratio. Data indicate selective barr iers (blood-brain and blood-CSF barriers) tio blood lymphocyte subsets whic h favor the transfer of T subsets. Correlation of the subset ratios to the CD3(+) ratio indicates distinct barrier properties which changed differentl y with acute and subacute inflammations and neuroimmunological diseases of central nervous system (CNS) in lumbar or ventricular CSF, but not with sim ple protein barrier disturbance. HLA DR+ T ratios were higher than HLA DR- T ratios only with controls and some neuroimmunological diseases. Lymphocyt e barrier characteristics were related tot protein leakage situated at the same barriers, indicating far the lymphocyte subsets selective transfer rou tes in control subjects and non-selective routes in patients with CNS infla mmation where altered ratios revealed a mixture of both routes.