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Multiple sclerosis: glatiramer acetate induces anti-inflammatory T cells in the cerebrospinal fluid
被引:32
作者:
Hestvik, A. L. K.
[1
]
Skorstad, G.
[2
]
Price, D. A.
[3
]
Vartdal, F.
[1
]
Holmoy, T.
[1
,2
]
机构:
[1] Rikshosp Radiumhosp, Inst Immunol, Fac Med, Oslo, Norway
[2] Ullevaal Univ Hosp, Dept Neurol, Oslo, Norway
[3] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DU, England
关键词:
multiple sclerosis;
immunology;
glatiramer acetate;
disease modifying therapies;
D O I:
10.1177/1352458508089411
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Glatiramer acetate (GA) is believed to induce GA-reactive T cells that secrete anti-inflammatory cytokines at the site of inflammation in multiple sclerosis (MS). However, GA-reactive T cells have not been established from the intrathecal compartment of MS patients, and intrathecal T cells may differ from T cells in blood. Here, we compared the phenotype of GA-reactive T cells from the cerebrospinal fluid (CSF) and blood of five MS patients treated with GA for 3-36 months, and in three of these patients also before treatment. From the CSF of these patients, all 22 T cell lines generated before and all 38 T cell lines generated during treatment were GA-reactive. GA treatment induced a more pronounced anti-inflammatory profile of GA-reactive T cell lines from CSF than from blood. While GA-reactive T cell clones from CSF were restricted by either human leukocyte antigen (HLA) -DR or HLA-DP, only HLA-DR restricted GA-reactive T cell clones were detected in blood. No cross reactivity with myelin proteins was detected in GA-reactive T cell lines or clones from CSF. These results suggest that a selected subset of GA-reactive T cells are present in the intrathecal compartment, and support an anti-inflammatory mechanism of action for GA.
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页码:749 / 758
页数:10
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