Serum matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 levels in patients with tick-borne encephalitis

被引:29
|
作者
Palus, Martin [1 ,2 ]
Zampachova, Eva [3 ]
Elsterova, Jana [1 ,2 ]
Ruzek, Daniel [1 ,4 ]
机构
[1] Acad Sci Czech Republ, Ctr Biol, Inst Parasitol, CZ-37005 Ceske Budejovice, Czech Republic
[2] Univ South Bohemia, Fac Sci, CZ-37005 Ceske Budejovice, Czech Republic
[3] Hosp Ceske Budejovice, Dept Virol, CZ-37001 Ceske Budejovice, Czech Republic
[4] Vet Res Inst, Dept Virol, CZ-62100 Brno, Czech Republic
关键词
Tick-borne encephalitis; Matrix metalloproteinase-9; Tissue inhibitor of metalloproteinase-1; Blood-brain barrier; BLOOD-BRAIN-BARRIER; MATRIX METALLOPROTEINASES; CEREBROSPINAL-FLUID; DISRUPTION; EXPRESSION; PROTEINS; INCREASE;
D O I
10.1016/j.jinf.2013.09.028
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1) play important roles in the function of the blood-brain barrier (BBB). To investigate the function of the BBB during tick-borne encephalitis (TBE), the levels of MMP-9 and its common tissue inhibitor, TIMP-1, were measured in serum from patients with acute phase of TBE. Methods: Serum MMP-9 and TIMP-1 levels were measured in 147 patients with TBE and 153 controls by ELISA. Results: Serum MMP-9 levels and MMP-9/TIMP-1 ratios of TBE patients were significantly higher than controls (p < 0.0001 and p < 0.005, respectively). There were no significant differences in serum TIMP-1 levels between TBE patients and controls. Serum MMP-9 and TIMP-1 levels and MMP-9/TIMP-1 ratios were not associated with age of the patients. However, TBE-positive males with TBE had higher levels of MMP-9 than TBE-positive females (p < 0.05). Conclusions: Our results suggest that the increased serum level of MMP-9 and MMP-9/TIMP-1 ratio is associated with the pathogenesis of TBE. Serum MMP-9 can serve as an indicator of breakdown of the BBB and inflammatory brain damage during TBE. (C) 2013 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:165 / 169
页数:5
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