Anderson K C, Bates M P, Slaughenhoupt B L, Pinkus G S, Schlossman S F, Nadler L M
Blood. 1984 Jun;63(6):1424-33.
A series of monoclonal antibodies that define B cell restricted and associated antigens was utilized in an attempt to characterize tumors of B lineage and to relate these tumors to B cell differentiative stages. Antigens that were previously shown to be B cell restricted on normal B lymphocytes were similarly expressed only on B cell malignancies. In contrast, antigens that were B cell associated were also found on tumors of other lineages. Moreover, on the basis of cell surface phenotypes, tumors of B cell origin were divided into three major subgroups, which corresponded to the level of differentiation of the malignant tumor cell: pre-B cell stage (non-T acute lymphoblastic leukemia and chronic myelocytic leukemia in lymphoid blast crisis); the mid-B cell stage (chronic lymphocytic leukemia, poorly differentiated lymphomas); and secretory B cell stage (large cell lymphomas and plasma cell tumors). A hypothetical model is derived that relates the malignant B cell to its normal cellular counterpart on the basis of cell surface expression of this panel of B cell-restricted and B cell-associated antigens.
一系列可定义B细胞限制性及相关抗原的单克隆抗体被用于试图对B系肿瘤进行特征描述,并将这些肿瘤与B细胞分化阶段相关联。先前显示在正常B淋巴细胞上具有B细胞限制性的抗原同样仅在B细胞恶性肿瘤上表达。相比之下,B细胞相关抗原也在其他谱系的肿瘤中被发现。此外,基于细胞表面表型,B细胞起源的肿瘤被分为三个主要亚组,这与恶性肿瘤细胞的分化水平相对应:前B细胞阶段(非T急性淋巴细胞白血病和淋巴细胞母细胞危象期的慢性粒细胞白血病);中B细胞阶段(慢性淋巴细胞白血病、低分化淋巴瘤);以及分泌性B细胞阶段(大细胞淋巴瘤和浆细胞瘤)。基于这组B细胞限制性和B细胞相关抗原的细胞表面表达,得出了一个将恶性B细胞与其正常细胞对应物相关联的假设模型。