CCR5 Δ32, matrix metalloproteinase-9 and disease activity in multiple sclerosis

被引:135
作者
Sellebjerg, F
Madsen, HO
Jensen, CV
Jensen, J
Garred, P
机构
[1] Univ Copenhagen, Glostrup Hosp, Dept Neurol, DK-2600 Glostrup, Denmark
[2] Statens Serum Inst, Sector Diagnost Serv, Dept Clin Biochem, DK-2300 Copenhagen S, Denmark
[3] Univ Copenhagen, Rigshosp, Dept Clin Immunol, DK-2200 Copenhagen N, Denmark
[4] Univ Copenhagen, Hvidovre Hosp, Danish Res Ctr Magnet Resonance Imaging, DK-2650 Hvidovre, Denmark
关键词
cerebrospinal fluid; chemokine; matrix metalloproteinase; multiple sclerosis; CD4 T cells;
D O I
10.1016/S0165-5728(99)00166-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines and matrix metalloproteinases (MMPs) appear to be crucial in leukocyte recruitment to the central nervous system in multiple sclerosis (MS). CCR5 Delta 32. a truncated allele of the CC chemokine receptor CCR5 gene encoding a non-functional receptor, did not confer protection from MS. CCR5 Delta 32 was, however, associated with a lower risk of recurrent clinical disease activity. High CSF levels of MMP-9 activity were also associated with recurrent disease activity. These results directly link intrathecal inflammation to disease activity in patients with MS, suggesting that treatments targeting CCR5 or treatment with MMP inhibitors may attenuate disease activity in MS. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:98 / 106
页数:9
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