Grogan T M, Rangel C S, Wirt D P, Richter L C, Bever F N, Jolley C S, Villar H V, Jones S E
Diagn Immunol. 1985;3(3):126-32.
Using a battery of monoclonal antibodies on snap-frozen sections, we delineated the immunoarchitecture of two splenic small cleaved cell lymphomas (SCL). Both cases had light- and heavy-chain restricted immunoglobulin (lg) expression signifying replacement of splenic white pulp by a single B-cell clone. Both the monotypia and aberrant topography of lg expression in SCL contrasted with the usual polyclonal, zonal lg expression in reactive splenic B-cell zones. Pan B antigens (B1, B4, and L14) were constant in expression as expected for B-cell neoplasms, while B-cell maturation antigens (B2, IgD, and CALLA) were variably expressed, suggesting that different SCL may derive from separate phases of B-cell ontogeny. Close association of SCL with dendritic reticulum cells suggests SCL may derive from splenic secondary follicles or home to these sites. The variable T-cell component detected by a T-cell panel (Leu 1-9) indicates the substantial range of T-cell reactivity in splenic SCL. We emphasize the immunologic aberrancy of splenic SCL when compared to normal splenic B-cell immunotopography. Further, we illustrate the utility of serial tissue section immunochemistry in revealing complex neoplastic cell phenotypes and in revealing the relationships of reactive cells to neoplastic cells.
我们使用一系列单克隆抗体对速冻切片进行检测,描绘了两例脾小裂细胞淋巴瘤(SCL)的免疫结构。两例病例均有轻链和重链受限的免疫球蛋白(Ig)表达,这表明单个B细胞克隆取代了脾白髓。SCL中Ig表达的单型性和异常分布与反应性脾B细胞区通常的多克隆、带状Ig表达形成对比。正如B细胞肿瘤所预期的那样,泛B抗原(B1、B4和L14)的表达是恒定的,而B细胞成熟抗原(B2、IgD和CALLA)的表达则各不相同,这表明不同的SCL可能源自B细胞个体发生的不同阶段。SCL与树突状网状细胞的密切关联表明SCL可能源自脾次级滤泡或定位于这些部位。通过T细胞抗体组合(Leu 1 - 9)检测到的可变T细胞成分表明脾SCL中T细胞反应性的范围很大。与正常脾B细胞免疫拓扑结构相比,我们强调了脾SCL的免疫异常。此外,我们阐述了连续组织切片免疫化学在揭示复杂肿瘤细胞表型以及揭示反应性细胞与肿瘤细胞关系方面的作用。