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Induced sputum-retrieved matrix metalloproteinase 9 and tissue metalloproteinase inhibitor 1 in granulomatous diseases

机译:肉芽肿病中诱导的痰回收基质金属蛋白酶9和组织金属蛋白酶抑制剂1

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摘要

Matrix metalloproteinases (MMPs) capable of degrading various components of connective tissue matrices, and tissue inhibitor metalloproteinases (TIMPs) are considered important in lung parenchymal remodeling and repair processes in pulmonary diseases. Induced sputum (IS) is a reliable noninvasive method to investigate pathogenesis, pathophysiology and treatment of lung disease. This study was designed to determine whether IS-MMP9/TIMP1 levels demonstrate lung parenchymal remodeling in sarcoidosis (SA) and Crohn's disease (CRD) patients. Sputum was induced and processed conventionally in 13 SA patients, 18 CRD patients and 9 controls. Two-hundred cells were counted on Giemsa-stained cytopreps, and T lymphocytes subsets (CD4 = T helper and CD8 = T suppressor cytotoxic cells) were analysed by FACS using monoclonal antibodies.MMP-9 and TIMP-1 were measured using commercial ELISA kits. MMP-9 concentrations, but not those of TIMP-1, were significantly greater in the sputum supernatant in SA and CRD patients compared to controls (P = 0·018 and P = 0·0019, respectively). The molar ratio, MMP-9/TIMP-1, was significantly higher in SA and CRD patients compared to controls (P = 0·008 and P = 0·024, respectively). Gelatinase species having a molecular weight similar to that of MMP-9 were demonstrated by zymographic analysis. MMP-9 levels were highly correlated with the CD4/CD8 ratio and DLCO capacity in SA but less in CRD patients. MMP-9 levels in IS provide a sensitive marker for pulmonary damage.
机译:能够降解结缔组织基质各种成分的基质金属蛋白酶(MMP)和组织抑制剂金属蛋白酶(TIMP)被认为在肺实质的肺实质重塑和修复过程中很重要。诱导痰(IS)是研究肺部疾病的发病机理,病理生理学和治疗方法的可靠的非侵入性方法。这项研究旨在确定IS-MMP9 / TIMP1水平是否显示结节病(SA)和克罗恩病(CRD)患者的肺实质重塑。按常规方法在13例SA患者,18例CRD患者和9例对照中诱导和处理痰。在Giemsa染色的细胞制备物中计数200个细胞,并使用单克隆抗体通过FACS分析T淋巴细胞亚群(CD4 = T辅助细胞和CD8 = T抑制细胞毒性细胞),并使用市售ELISA试剂盒测量MMP-9和TIMP-1 。与对照组相比,SA和CRD患者的痰液上清液中MMP-9的浓度显着更高,而TIMP-1的浓度则显着更高(分别为P = 0.018和P = 0.0019)。与对照组相比,SA和CRD患者的摩尔比MMP-9 / TIMP-1显着更高(分别为P = 0·008和P = 0·024)。通过酶谱分析证实分子量与MMP-9相似的明胶酶种类。 MMP-9水平与SA中CD4 / CD8比和DLCO容量高度相关,而在CRD患者中较少。 IS中的MMP-9水平为肺损伤提供了敏感的标志。

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