Freedman A S, Pedrazzini A, Nadler L M
Dana-Farber Cancer Institute, Department of Medicine, Harvard Medical School, Boston, Massachusetts.
Cancer Invest. 1991;9(1):69-84. doi: 10.3109/07357909109032802.
The use of MAbs directed against B-cell markers has identified considerably more heterogeneity within B-cell neoplasms than was evident by standard morphologic and histochemical techniques. Using markers specific for lineage and state of differentiation, it is possible to correlate malignant B cells to their normal cellular counterparts. Considering the complexity of normal B-cell ontogeny, differentiation, and function, it is not surprising that these malignancies reflect this diversity. Hopefully, with increasing characterization of the normal function of cell surface molecules, as well as the subpopulations of normal cells to which these malignancies correspond, we will have a better understanding of the biologic and clinical behavior of these malignancies.
与标准形态学和组织化学技术相比,针对B细胞标志物的单克隆抗体(MAbs)的使用已在B细胞肿瘤中发现了更多的异质性。利用针对谱系和分化状态的特异性标志物,可以将恶性B细胞与其正常细胞对应物相关联。考虑到正常B细胞个体发育、分化和功能的复杂性,这些恶性肿瘤反映这种多样性也就不足为奇了。有望随着对细胞表面分子正常功能以及这些恶性肿瘤所对应的正常细胞亚群的特征描述不断增加,我们将更好地理解这些恶性肿瘤的生物学和临床行为。