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首页> 外文期刊>BMC Infectious Diseases >Title: role of matrix metalloproteinase ?9 in progression of tuberculous meningitis: a pilot study in patients at different stages of the disease
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Title: role of matrix metalloproteinase ?9 in progression of tuberculous meningitis: a pilot study in patients at different stages of the disease

机译:发言题目:基质金属蛋白酶α9在结核性脑膜炎进展中的作用:该病不同阶段患者的一项初步研究

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Background TBM (Tuberculous meningitis) is severe form of tuberculosis causing death of one third of the affected individuals or leaving two-third of the survivors disabled. MMP-9 (Matrix metalloproteinase-9) is produced by the central nervous system in a variety of inflammatory conditions and has a role in the breakdown of extracellular matrix and blood–brain barrier. Methods In this study, the levels of MMP-9 and its inhibitor, TIMP-1 (tissue inhibitor of metalloproteinases-1), were screened using zymography and reverse zymography in cerebrospinal fluid and serum of tuberculous meningitis patients at different stages of the disease. Further, role of MMP-9 as therapeutic target was studied in C6 glioma cells infected with Mycobacterium tuberculosis H37Rv. Cells were treated with dexamethasone or SB-3CT (specific inhibitor of MMP-9) in combination with conventional antitubercular drugs. Results MMP-9 levels in patients were increased as the disease progressed to advanced stages. The infection led to increased MMP-9 levels in C6 glioma cells and specific inhibition of MMP-9 by SB-3CT augmented bacillary clearance when used along with antitubercular drugs. Conclusion MMP-9 plays a prominent role in progression of tuberculous meningitis from initial to advanced stages. Increased levels of MMP-9 during advancement of the disease leads to degeneration of nervous tissue and blood brain barrier disruption. Hence, MMP-9 can be considered as a therapeutic target for efficient management of TBM and can be explored to inhibit further progression of the disease if used at an early stage.
机译:背景技术TBM(结核性脑膜炎)是一种严重的结核病,导致三分之一的受感染者死亡或三分之二的幸存者致残。 MMP-9(基质金属蛋白酶-9)由中枢神经系统在多种炎症条件下产生,并在细胞外基质和血脑屏障的分解中起作用。方法在这项研究中,采用酶谱和反向酶谱法对结核性脑膜炎患者在不同疾病阶段的MMP-9及其抑制剂TIMP-1(金属蛋白酶的组织抑制剂)的水平进行了筛选。此外,在感染了结核分枝杆菌H 37 R v 的C6神经胶质瘤细胞中研究了MMP-9作为治疗靶标的作用。用地塞米松或SB-3CT(MMP-9的特异性抑制剂)与常规抗结核药联合治疗细胞。结果随着疾病进展到晚期,患者的MMP-9水平升高。当与抗结核药物一起使用时,感染导致C6胶质瘤细胞中MMP-9水平升高,并且SB-3CT增强了细菌清除率,从而特异性抑制了MMP-9。结论MMP-9在结核性脑膜炎从初期到晚期的发展中起着重要作用。在疾病发展过程中,MMP-9水平升高会导致神经组织变性和血脑屏障破坏。因此,MMP-9可以被认为是有效管理TBM的治疗靶标,并且如果在早期使用,则可以被探索为抑制疾病的进一步发展。

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