Higashi-Kuwata Nobuyo, Makino Takamitsu, Inoue Yuji, Takeya Motohiro, Ihn Hironobu
Exp Dermatol. 2009 Aug;18(8):727-9. doi: 10.1111/j.1600-0625.2008.00828.x. Epub 2009 Mar 3.
Localized scleroderma is a connective tissue disorder that is limited to the skin and subcutaneous tissue. Macrophages have been reported to be particularly activated in patients with skin disease including systemic sclerosis and are potentially important sources for fibrosis-inducing cytokines, such as transforming growth factor beta. To clarify the features of immunohistochemical characterization of the immune cell infiltrates in localized scleroderma focusing on macrophages, skin biopsy specimens were analysed by immunohistochemistry. The number of cells stained with monoclonal antibodies, CD68, CD163 and CD204, was calculated. An evident macrophage infiltrate and increased number of alternatively activated macrophages (M2 macrophages) in their fibrotic areas were observed along with their severity of inflammation. This study revealed that alternatively activated macrophages (M2 macrophages) may be a potential source of fibrosis-inducing cytokines in localized scleroderma, and may play a crucial role in the pathogenesis of localized scleroderma.
局限性硬皮病是一种局限于皮肤和皮下组织的结缔组织疾病。据报道,巨噬细胞在包括系统性硬化症在内的皮肤病患者中特别活跃,并且可能是诱导纤维化细胞因子(如转化生长因子β)的重要来源。为了阐明以巨噬细胞为重点的局限性硬皮病免疫细胞浸润的免疫组织化学特征,通过免疫组织化学分析了皮肤活检标本。计算用单克隆抗体CD68、CD163和CD204染色的细胞数量。观察到在其纤维化区域有明显的巨噬细胞浸润和交替活化巨噬细胞(M2巨噬细胞)数量增加,以及炎症严重程度。这项研究表明,交替活化巨噬细胞(M2巨噬细胞)可能是局限性硬皮病中诱导纤维化细胞因子的潜在来源,并可能在局限性硬皮病的发病机制中起关键作用。