Sarsfield P, Jones D B, Wotherspoon A C, Harvard T, Wright D H
University Department of Pathology, Southampton General Hospital, U.K.
J Pathol. 1996 Sep;180(1):18-25. doi: 10.1002/(SICI)1096-9896(199609)180:1<18::AID-PATH624>3.0.CO;2-V.
This paper presents a description of the patterns of distribution of accessory cells in helicobacter gastritis and low-grade gastric MALT lymphomas. The use of gastric resection specimens afforded abundant, well-orientated lymphoid tissue. Fifteen cases were selected from patients with MALT lymphomas, three with gastritis alone, and six histologically normal controls. A panel of antibodies working in paraffin-embedded tissue, identifying differing accessory cells, was used. These comprised antibodies to HLA class II (WR18), acid cysteine proteinase inhibitor (ACPI), CD68 (PGM1), Factor XIIIa, S100 protein, CD23 (BU38), CD106 (V-CAM1), CD55 (BRIC 128), and CD21 (1F8). CD68-positive macrophages in the gastritis cases were abundant in the superficial mucosa. Factor XIIIa also identified dendritic cells at deeper sites but these were absent from both the acquired and the neoplastic lymphoid tissue. Antibodies to both S100 protein and ACPI stained dendritic cells localized to areas within and adjacent to the lymphoid tissue only. S100 protein-positive cells were concentrated in close contact with glandular epithelium immediately above the germinal centres, while ACPI-positive dendritic cells were identified, especially around the more blastic reactive follicles, in the intervening space between the germinal centres and the overlying epithelium. Similar patterns of organization were also seen in the areas of mucosal lymphoma. The follicular dendritic markers revealed overlapping but distinct sub-populations within the germinal centres which appeared to alter depending on the activity of the germinal centres. While both ACPI and CD55 stained the germinal centre dendritic reticulum cell networks only, CD21 and CD106 also stained the mantle dendritic cells. The proportion staining with CD23, which stains dendritic reticulum cells within the centrocyte-rich areas of the germinal centres only, was greatest in the more quiescent germinal centres. Similar patterns of staining were also seen in germinal centres within the gastric MALT lymphomas. It is proposed that the sub-populations of dendritic cells staining with S100 protein and ACPI may facilitate helicobacter antigen delivery to the germinal centres. The follicular dendritic cells then promote a sustained B-cell response to the luminal pathogen.
本文描述了幽门螺杆菌胃炎和低度胃黏膜相关淋巴组织淋巴瘤中辅助细胞的分布模式。胃切除标本提供了丰富且方向良好的淋巴组织。从黏膜相关淋巴组织淋巴瘤患者中选取了15例,3例仅患有胃炎,以及6例组织学正常的对照。使用了一组针对石蜡包埋组织的抗体,以识别不同的辅助细胞。这些抗体包括针对II类人类白细胞抗原(WR18)、酸性半胱氨酸蛋白酶抑制剂(ACPI)、CD68(PGM1)、凝血因子XIIIa、S100蛋白、CD23(BU38)、CD106(V-CAM1)、CD55(BRIC 128)和CD21(1F8)的抗体。胃炎病例中CD68阳性巨噬细胞在浅表黏膜中丰富。凝血因子XIIIa也在较深部位识别出树突状细胞,但在获得性和肿瘤性淋巴组织中均未发现。针对S100蛋白和ACPI的抗体仅对位于淋巴组织内及其相邻区域的树突状细胞进行染色。S100蛋白阳性细胞集中在与生发中心上方的腺上皮紧密接触处,而ACPI阳性树突状细胞则在生发中心与上皮之间的间隙中被识别出来,尤其是在更具母细胞性的反应性滤泡周围。在黏膜淋巴瘤区域也观察到了类似的组织模式。滤泡树突状细胞标志物显示出生发中心内重叠但不同的亚群,这些亚群似乎会根据生发中心的活性而改变。虽然ACPI和CD55仅对生发中心树突状网状细胞网络进行染色,但CD21和CD106也对套区树突状细胞进行染色。仅对生发中心富含中心细胞区域内的树突状网状细胞进行染色的CD23的染色比例在较静止的生发中心中最大。在胃黏膜相关淋巴组织淋巴瘤的生发中心也观察到了类似的染色模式。有人提出,用S100蛋白和ACPI染色的树突状细胞亚群可能有助于将幽门螺杆菌抗原递送至生发中心。然后滤泡树突状细胞促进对腔内病原体的持续B细胞反应。