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Published on: February 2, 2011
Central memory CD4+ T cells dominate the normal cerebrospinal fluid
Marieke T de Graaf1, Peter A E Sillevis Smitt, Ronald L Luitwieler
1Department of Neurology, Erasmus University Medical Center, s-Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands.
Insights
Establishing reference values for white blood cell (WBC) subsets in cerebrospinal fluid (CSF) is crucial for diagnosing neuro-inflammatory diseases. This study found a predominance of CD4(+) T cells with a central memory phenotype in CSF, suggesting active immune responses in the central nervous system (CNS).
Area of Science:
- Neuroimmunology
- Immunology
- Cell Biology
Background:
- Cerebrospinal fluid (CSF) immune phenotyping requires established reference values for white blood cell (WBC) subsets.
- Understanding normal immune cell populations in CSF is vital for diagnosing and researching neuro-inflammatory conditions.
Purpose of the Study:
- To establish reference values for WBC subsets in CSF using immune phenotyping.
- To characterize the distribution and phenotype of immune cells in the central nervous system (CNS) under normal conditions.
Main Methods:
- 6-color flow cytometry was used to analyze paired CSF and blood samples from 84 healthy individuals.
- Absolute counts and percentages of various leukocyte subsets, including lymphocytes (T, NK, NKT, B cells), granulocytes, monocytes, and dendritic cells, were quantified.
- T cell subsets were further analyzed for naive, central memory, effector memory, and regulatory phenotypes.
Main Results:
- CSF demonstrated a higher proportion of T cells compared to blood, with granulocytes, B cells, and NK cells being less frequent.
- CD4(+) T cells constituted the majority (approximately 70%) of T cells in CSF, predominantly exhibiting a central memory phenotype (approximately 90%).
- B cells were nearly absent (<1%) in CSF, while myeloid dendritic cells were more abundant than plasmacytoid dendritic cells in CSF compared to blood.
Conclusions:
- The study provides essential reference values for WBC subsets in CSF, aiding in the investigation of neuro-inflammatory diseases.
- The significant presence of CD4(+) T cells with a central memory phenotype and dendritic cells in CSF indicates an active adaptive immune response in the normal CNS.
Background:
To use cerebrospinal fluid (CSF) immune phenotyping as a diagnostic and research tool, we have set out to establish reference values of white blood cell (WBC) subsets in CSF.
Methods:
We assessed the absolute numbers and percentages of WBC subsets by 6-color flow cytometry in paired CSF and blood samples of 84 individuals without neurological disease who underwent spinal anaesthesia for surgery. Leukocyte (i.e., lymphocytes, granulocytes, and monocytes), lymphocyte (i.e., T [CD4(+) and CD8(+) ], NK, NKT and B cells), T cell (i.e., naïve, central memory, effector memory, and regulatory) and dendritic cell subsets (i.e., myeloid and plasmacytoid) were studied.
Results:
CSF showed a predominance of T cells, while granulocytes, B and NK cells were relatively rare compared to blood. The majority of T cells in CSF consisted of CD4(+) T cells (∼70%), most of them (∼90%) with a central memory phenotype, while B cells were almost absent (<1%). Among the small population of dendritic cells in CSF, those of the myeloid subtype were more frequent than plasmacytoid dendritic cells (medians: 1.7% and 0.4% of leukocytes, respectively), whilst both subsets made up 0.2% of leukocytes in blood.
Conclusions:
This study reports reference values of absolute numbers and percentages of WBC subsets in CSF, which are essential for further investigation of the immunopathogenesis of neuro-inflammatory diseases. Furthermore, the relative abundance of CD4(+) T cells, mainly with a central memory phenotype, and the presence of dendritic cells in CSF suggests an active adaptive immune response under normal conditions in the central nervous system (CNS).
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