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Th17/Th1 phenotype in demyelinating disease
被引:43
|作者:
Edwards, L. J.
[1
]
Robins, R. A.
[2
]
Constantinescu, C. S.
[1
]
机构:
[1] Queens Med Ctr, Sch Med, Div Clin Neurol, Nottingham NG7 2UH, England
[2] Queens Med Ctr, Div Clin Immunol, Nottingham NG7 2UH, England
来源:
关键词:
Multiple sclerosis;
Th17;
CD154;
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS;
MESSENGER-RNA EXPRESSION;
MULTIPLE-SCLEROSIS;
T-CELLS;
CD40;
LIGAND;
INFLAMMATORY DISEASES;
T(H)17 CELLS;
TH1;
INTERLEUKIN-17;
INTERFERON;
D O I:
10.1016/j.cyto.2009.12.003
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Background: Th17 cells are thought to contribute to the immunopathology of allergic and autoimmune conditions. Their role in multiple sclerosis (MS) pathology remains to be fully elucidated. Objective: To assess peripheral blood Th17 responses in patients with MS compared to controls. Methods: We isolated peripheral blood mononuclear cells from 41 MS patients and 23 healthy controls, which were then stimulated using phorbol ester and ionomycin, labelled for CD3, CD8, CD154, IL-17 and IFN-gamma and analysed using flow cytometry. Results: Minimal IL-17 was detectable in unstimulated cells. Following stimulation with phorbol ester and ionomycin. PBMCs taken from MS patients in relapse developed a more inflammatory profile than those taken from controls or non-relapse patients, with greater expression of CD154, IL-17 and dual expression of IL-17/IFN-gamma. Conclusion: We suggest a greater tendency to Th17 and Th1/Th17 response to non-specific stimulation in MS patients in relapse compared to controls and non-relapse patients. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:19 / 23
页数:5
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