Forbes G M, Horne R, Erber W N, Collins B J, Papadimitriou J M
Department of Gastroenterology, Royal Perth Hospital, Perth, WA.
Pathology. 1996 Aug;28(3):251-4. doi: 10.1080/00313029600169094.
Previous studies have demonstrated upregulation of intestinal mucosal macrophage CD16 (an Fc receptor for IgG) in bone marrow transplant (BMT) recipients with graft-versus-host disease (GVHD). We sought to determine whether there was ultrastructural evidence of mucosal macrophage activation in allogeneic BMT recipients and relate appearances to those seen in autologous BMT patients and to immunohistological findings. Sigmoid colonic mucosal biopsies from five allogeneic and three autologous BMT patients were taken prior to, 30 days after transplant and, in three of the allogeneic patients, 120 days after transplant. These were examined by immunohistochemistry and electron microscopy. Immunohistological analysis revealed upregulation of lamina propria macrophage CD16 after transplant in all patients except one autologous BMT recipient; there were no such changes in total macrophage numbers. Ultrastructural evidence of lamina propria macrophage activation was prominent after both allogeneic and autologous BMT. There was an increase in nuclear size accompanied by increased euchromatin and larger nucleoli. In the cytoplasm there were increased numbers of lysosomes, many of which were small and cylindrical, and cytoplasmic flaps were prominent. Phagosomes were less numerous after transplant. These data confirm that after BMT intestinal mucosal macrophages become activated. However changes in macrophage ultrastructure specific to patients at risk of developing clinical GVHD are lacking.
先前的研究表明,在患有移植物抗宿主病(GVHD)的骨髓移植(BMT)受者中,肠道黏膜巨噬细胞CD16(一种IgG的Fc受体)上调。我们试图确定在异基因BMT受者中是否存在黏膜巨噬细胞活化的超微结构证据,并将其表现与自体BMT患者的表现以及免疫组织学结果相关联。在移植前、移植后30天以及在三名异基因患者中在移植后120天,采集了五名异基因和三名自体BMT患者的乙状结肠黏膜活检组织。对这些组织进行了免疫组织化学和电子显微镜检查。免疫组织学分析显示,除一名自体BMT受者外,所有患者移植后固有层巨噬细胞CD16上调;巨噬细胞总数没有此类变化。在异基因和自体BMT后,固有层巨噬细胞活化的超微结构证据都很突出。核大小增加,同时常染色质增加,核仁增大。细胞质中溶酶体数量增加,其中许多是小的圆柱形,细胞质襟片突出。移植后吞噬体数量较少。这些数据证实,BMT后肠道黏膜巨噬细胞被激活。然而,缺乏针对有发生临床GVHD风险患者的巨噬细胞超微结构变化。