Increased frequency of CD4+ CD25+ regulatory T cells in the cerebrospinal fluid but not in the blood of multiple sclerosis patients

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Increased frequency of CD4+ CD25+ regulatory T cells in the cerebrospinal fluid but not in the blood of multiple sclerosis patients. / Feger, U; Luther, C; Poeschel, S; Melms, A; Tolosa, E; Wiendl, H.

in: CLIN EXP IMMUNOL, Jahrgang 147, Nr. 3, 01.03.2007, S. 412-8.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{a81333fd769d419794eda2fc089953e2,
title = "Increased frequency of CD4+ CD25+ regulatory T cells in the cerebrospinal fluid but not in the blood of multiple sclerosis patients",
abstract = "Naturally occurring CD4+ CD25+ regulatory T cells (nTreg) play a major role in controlling autoimmunity by suppressing self-reactive T cells. Multiple sclerosis (MS) is an inflammatory demyelinating disorder of the central nervous system (CNS), where T cells play a key role in orchestrating tissue damage. While CD4+ CD25+ nTreg have been investigated in peripheral blood from MS patients, little is known about their presence and possible function within the target organ, the CNS. In order to study whether these cells are present in the cerebrospinal fluid (CSF) under pathological conditions, we have analysed the frequency of CD4+ CD25+ nTreg in peripheral blood and CSF from MS patients (n=14), patients with other neurological disorders (OND; n=9) and compared peripheral levels with healthy controls (n=40). We found that the frequency of CD4+ CD25+ forkhead transcription factor 3 (FOXP3)+ nTreg was significantly elevated in the CSF from MS patients (mean CSF=4 x 05 +/- 1.54% versus mean peripheral blood = 2 x 93 +/- 0 x 94%) but not from patients with other neurological disorders (mean CSF = 3 x 78 +/- 1 x 26% versus mean peripheral blood = 3 x 74 +/- 1 x 4%). The frequency of nTreg in the periphery did not differ between MS patients and healthy donors; however, nTreg from MS patients showed reduced suppressive capacity.",
keywords = "Adult, Aged, Aged, 80 and over, Autoimmune Diseases, Cells, Cultured, Female, Forkhead Transcription Factors, Humans, Immune Tolerance, Interleukin-2 Receptor alpha Subunit, Male, Middle Aged, Multiple Sclerosis, Nervous System Diseases, T-Lymphocyte Subsets, T-Lymphocytes, Regulatory",
author = "U Feger and C Luther and S Poeschel and A Melms and E Tolosa and H Wiendl",
year = "2007",
month = mar,
day = "1",
doi = "10.1111/j.1365-2249.2006.03271.x",
language = "English",
volume = "147",
pages = "412--8",
journal = "CLIN EXP IMMUNOL",
issn = "0009-9104",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - Increased frequency of CD4+ CD25+ regulatory T cells in the cerebrospinal fluid but not in the blood of multiple sclerosis patients

AU - Feger, U

AU - Luther, C

AU - Poeschel, S

AU - Melms, A

AU - Tolosa, E

AU - Wiendl, H

PY - 2007/3/1

Y1 - 2007/3/1

N2 - Naturally occurring CD4+ CD25+ regulatory T cells (nTreg) play a major role in controlling autoimmunity by suppressing self-reactive T cells. Multiple sclerosis (MS) is an inflammatory demyelinating disorder of the central nervous system (CNS), where T cells play a key role in orchestrating tissue damage. While CD4+ CD25+ nTreg have been investigated in peripheral blood from MS patients, little is known about their presence and possible function within the target organ, the CNS. In order to study whether these cells are present in the cerebrospinal fluid (CSF) under pathological conditions, we have analysed the frequency of CD4+ CD25+ nTreg in peripheral blood and CSF from MS patients (n=14), patients with other neurological disorders (OND; n=9) and compared peripheral levels with healthy controls (n=40). We found that the frequency of CD4+ CD25+ forkhead transcription factor 3 (FOXP3)+ nTreg was significantly elevated in the CSF from MS patients (mean CSF=4 x 05 +/- 1.54% versus mean peripheral blood = 2 x 93 +/- 0 x 94%) but not from patients with other neurological disorders (mean CSF = 3 x 78 +/- 1 x 26% versus mean peripheral blood = 3 x 74 +/- 1 x 4%). The frequency of nTreg in the periphery did not differ between MS patients and healthy donors; however, nTreg from MS patients showed reduced suppressive capacity.

AB - Naturally occurring CD4+ CD25+ regulatory T cells (nTreg) play a major role in controlling autoimmunity by suppressing self-reactive T cells. Multiple sclerosis (MS) is an inflammatory demyelinating disorder of the central nervous system (CNS), where T cells play a key role in orchestrating tissue damage. While CD4+ CD25+ nTreg have been investigated in peripheral blood from MS patients, little is known about their presence and possible function within the target organ, the CNS. In order to study whether these cells are present in the cerebrospinal fluid (CSF) under pathological conditions, we have analysed the frequency of CD4+ CD25+ nTreg in peripheral blood and CSF from MS patients (n=14), patients with other neurological disorders (OND; n=9) and compared peripheral levels with healthy controls (n=40). We found that the frequency of CD4+ CD25+ forkhead transcription factor 3 (FOXP3)+ nTreg was significantly elevated in the CSF from MS patients (mean CSF=4 x 05 +/- 1.54% versus mean peripheral blood = 2 x 93 +/- 0 x 94%) but not from patients with other neurological disorders (mean CSF = 3 x 78 +/- 1 x 26% versus mean peripheral blood = 3 x 74 +/- 1 x 4%). The frequency of nTreg in the periphery did not differ between MS patients and healthy donors; however, nTreg from MS patients showed reduced suppressive capacity.

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Autoimmune Diseases

KW - Cells, Cultured

KW - Female

KW - Forkhead Transcription Factors

KW - Humans

KW - Immune Tolerance

KW - Interleukin-2 Receptor alpha Subunit

KW - Male

KW - Middle Aged

KW - Multiple Sclerosis

KW - Nervous System Diseases

KW - T-Lymphocyte Subsets

KW - T-Lymphocytes, Regulatory

U2 - 10.1111/j.1365-2249.2006.03271.x

DO - 10.1111/j.1365-2249.2006.03271.x

M3 - SCORING: Journal article

C2 - 17302889

VL - 147

SP - 412

EP - 418

JO - CLIN EXP IMMUNOL

JF - CLIN EXP IMMUNOL

SN - 0009-9104

IS - 3

ER -