Young L, Katrib A, Cuello C, Vollmer-Conna U, Bertouch J V, Roberts-Thomson P J, Ahern M J, Smith M D, Youssef P P
Prince of Wales Hospital, Sydney, New South Wales, Australia.
Arthritis Rheum. 2001 Feb;44(2):343-50. doi: 10.1002/1529-0131(200102)44:2<343::AID-ANR52>3.0.CO;2-Q.
To investigate the effects of intraarticular glucocorticoid treatment on macrophage infiltration, the expression of the chemokines monocyte chemoattractant protein 1 (MCP-1) and macrophage inflammatory protein 1alpha (MIP-1alpha), and the expression of matrix metalloproteinases 1 and 3 (MMPs 1 and 3) and their inhibitors, the tissue inhibitors of metalloproteinases 1 and 2 (TIMPs 1 and 2), in osteoarthritis (OA) synovial membranes.
Forty patients underwent arthroscopic biopsy before and 1 month after intraarticular injection of glucocorticoids. Twenty-one patients received 120 mg of methylprednisolone acetate (Depo-Medrol; Upjohn, Kalamazoo, MI), and 20 patients received placebo (1 patient received placebo in 1 knee and methylprednisolone acetate in the other). Immunoperoxidase staining for the expression of CD68, MCP-1, MIP-1alpha, MMP-1, MMP-3, TIMP-1, and TIMP-2 was performed, and the immunostaining was quantified by color video image analysis.
CD68, MCP-1, MIP-1alpha, MMP-1, MMP-3, TIMP-1, and TIMP-2 immunostaining was observed in all synovial membranes. Intraarticular glucocorticoid treatment was associated with a small (30%) but statistically significant (P = 0.048) reduction in CD68+ macrophage staining in the synovial lining layer, but there was no change in the CD68 expression in the synovial sublining layer. No significant differences were observed for MCP-1, MIP-1alpha, MMP-1, MMP-3, TIMP-1, and TIMP-2 immunostaining in the synovial lining or sublining layers.
Intraarticular glucocorticoids may reduce CD68+ macrophage infiltration into the synovial lining layer, but not the expression of MCP-1, MIP-1alpha, MMP-1, MMP-3, TIMP-1, and TIMP-2 in the synovial membrane, in patients with OA.
研究关节内注射糖皮质激素对骨关节炎(OA)滑膜中巨噬细胞浸润、趋化因子单核细胞趋化蛋白1(MCP-1)和巨噬细胞炎性蛋白1α(MIP-1α)的表达、基质金属蛋白酶1和3(MMP-1和MMP-3)及其抑制剂金属蛋白酶组织抑制剂1和2(TIMP-1和TIMP-2)表达的影响。
40例患者在关节内注射糖皮质激素前及注射后1个月接受关节镜活检。21例患者接受120mg醋酸甲泼尼龙(得宝松;Upjohn公司,卡拉马祖,密歇根州),20例患者接受安慰剂(1例患者一侧膝关节接受安慰剂,另一侧接受醋酸甲泼尼龙)。对CD68、MCP-1、MIP-1α、MMP-1、MMP-3、TIMP-1和TIMP-2的表达进行免疫过氧化物酶染色,并通过彩色视频图像分析对免疫染色进行定量。
在所有滑膜中均观察到CD68、MCP-1、MIP-1α、MMP-1、MMP-3、TIMP-1和TIMP-2免疫染色。关节内注射糖皮质激素治疗使滑膜衬里层CD68+巨噬细胞染色减少了30%,差异虽小,但具有统计学意义(P = 0.048),而滑膜下层CD68表达无变化。滑膜衬里层或下层中MCP-1、MIP-1α、MMP-1、MMP-3、TIMP-1和TIMP-2免疫染色未观察到显著差异。
对于OA患者,关节内注射糖皮质激素可能会减少CD68+巨噬细胞向滑膜衬里层的浸润,但不会改变滑膜中MCP-1、MIP-1α、MMP-1、MMP-3、TIMP-1和TIMP-2的表达。