Payne S V, Wright D H, Jones K J, Judd M A
J Clin Pathol. 1982 Feb;35(2):159-66. doi: 10.1136/jcp.35.2.159.
In an immunohistochemical study of 26 biopsies from 24 patients with Hodgkin's disease a granular staining pattern for alpha-1-antitrypsin (alpha(1)AT) and alpha-1-antichymotrypsin (alpha(1)ACT) was seen in Reed-Sternberg (RS) cells and mononuclear Hodgkin's (H) cells in over half the cases. The pattern of staining for these antiproteases seen in RS and H cells has previously only been observed in normal and malignant cells of the monocyte/macrophage lineage within the lymphoreticular system. A faintly granular evenly distributed staining for IgG was found in viable RS and H cells. This staining was associated with a similar distribution of both light chains but not J chain, suggesting that the immunoglobulin had not been synthesised by these cells but had been taken up from the extracellular environment. It is suggested that this uptake is an active process occurring in viable RS and H cells, possibly via Fcgamma receptors and further supports an origin from cells of the monocyte/macrophage lineage. IgA, IgD, albumin, fibrinogen, C1q, C4 and C3 were present in some cells, IgM was more rarely found and lysozyme was absent. The fact that cells staining for these serum proteins generally showed signs of degeneration and that the extent of staining correlated with the molecular weight, but not serum concentration, of the protein suggests that they are passively acquired by dead or dying cells and thus represent a separate phenomenon from IgG uptake. The function of IgG uptake and accumulation by RS cells and the alpha(1)AT and alpha(1)ACT markers may prove of use in identifying the macrophage subtype from which these cells are derived.
在一项对24例霍奇金病患者的26份活检标本进行的免疫组织化学研究中,超过半数病例的里德-斯腾伯格(RS)细胞和单核霍奇金(H)细胞中可见α-1抗胰蛋白酶(α1AT)和α-1抗糜蛋白酶(α1ACT)呈颗粒状染色模式。此前,仅在淋巴网状系统内单核细胞/巨噬细胞系的正常和恶性细胞中观察到RS细胞和H细胞中这些抗蛋白酶的染色模式。在存活的RS细胞和H细胞中发现IgG呈微弱颗粒状均匀分布染色。这种染色与两条轻链的类似分布相关,但与J链无关,这表明免疫球蛋白不是由这些细胞合成的,而是从细胞外环境摄取的。提示这种摄取是存活的RS细胞和H细胞中发生的一个活跃过程,可能通过Fcγ受体进行,进一步支持其起源于单核细胞/巨噬细胞系的细胞。一些细胞中存在IgA、IgD、白蛋白、纤维蛋白原、C1q、C4和C3,IgM较少见,溶菌酶不存在。这些血清蛋白染色的细胞通常显示退变迹象,且染色程度与蛋白质的分子量相关,而与血清浓度无关,这一事实表明它们是由死亡或濒死细胞被动获得的,因此代表了一种与IgG摄取不同的现象。RS细胞摄取和积累IgG以及α1AT和α1ACT标志物的功能可能有助于识别这些细胞所衍生的巨噬细胞亚型。