GM-CSF production by CD4+ T cells in MS patients: Regulation by regulatory T cells and vitamin D

被引:13
作者
Peelen, E. [1 ,2 ,3 ]
Muris, A. -H. [1 ,2 ,3 ]
Damoiseaux, J. [4 ]
Knippenberg, S. [1 ,2 ,3 ]
Broens, K. [5 ]
Smolders, J. [1 ]
Tervaert, J. W. Cohen [6 ]
Hupperts, R. [1 ,2 ]
Thewissen, M. [3 ]
机构
[1] Maastricht Univ, Med Ctr, Sch Mental Hlth & Neurosci, NL-6202 AZ Maastricht, Netherlands
[2] Orbis Med Ctr, Dept Neurol, Acad MS Ctr Limburg, Sittard, Netherlands
[3] Maastricht Univ, Med Ctr, Div Clin & Expt Immunol, Dept Internal Med, NL-6202 AZ Maastricht, Netherlands
[4] Maastricht Univ, Med Ctr, Cent Diagnost Lab, NL-6202 AZ Maastricht, Netherlands
[5] Orbis Med Ctr, Dept Clin Chem & Hematol, Sittard, Netherlands
[6] Maastricht Univ, Med Ctr, NL-6202 AZ Maastricht, Netherlands
关键词
Multiple sclerosis; T helper cell; GM-CSF; Regulatory T cell; Vitamin D; COLONY-STIMULATING FACTOR; MULTIPLE-SCLEROSIS PATIENTS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CEREBROSPINAL-FLUID; POTASSIUM CHANNEL; DENDRITIC CELLS; HELPER-CELLS; CYTOKINE; EXPRESSION; INFLAMMATION;
D O I
10.1016/j.jneuroim.2015.02.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background/objective: Data from animal models of MS suggest that GM-CSF(+)CD4(+)T cells are pathogenic cells. Therefore, GM-CSF production by CD4(+)T cells of MS patients and their susceptibility to regulatory mechanisms were investigated. Methods: Intracellular flowcytometry was performed to determine the GM-CSF(+)CD4(+)T cell fraction in PBMC and CSF of MS patients and controls. The effect of regulatory T cells (Tregs) on GM-CSF production by CD4(+)T cells was studied in MS patients using a proliferation-suppression assay. Finally, GM-CSF(+)CD4(+)T cell fraction and GM-CSF protein levels in supernatant were assessed in anti-CD3-stimulated CD4(+)T cell cultures derived from healthy controls and MS patients, in the presence or absence of the active vitamin D metabolite calcitriol. Results: The GM-CSF(+)CD4(+)T cell fraction in the peripheral blood did not differ between controls and MS patients. This T cell population could also be detected in the CSF of both subjects with MS as well as subjects with another diagnosis. In the CSF, it comprised a significant fraction of the T cell population. Upon in vitro stimulation of PBMC with anti-CD3 antibody, no differences were observed in GM-CSF(+)CD4(+)T cell frequencies. GM-CSF secretion was susceptible to regulation by Treg and vitamin D. Suppression of GM-CSF secretion by vitamin D was reduced in MS patients. Conclusions: Our study showed no elevation in GM-CSF(+)CD4(+)T cell fractions in MS patients compared to controls. Furthermore, GM-CSF secretion was prone to regulation by Treg and vitamin D, the latter being less effective in MS patients. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:36 / 42
页数:7
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