Centola M, Lin K, Sutton C, Berenson J R, Kunkel L A, Rosen L, Hahn B H, Robinson R R
XOMA Corporation, Santa Monica, California, USA.
Leuk Lymphoma. 1996 Feb;20(5-6):465-69. doi: 10.3109/10428199609052430.
We have assessed the specificity of antibodies from the leukemic B cells of five patients with both chronic lymphocytic leukemia and autoimmune hemolytic anemia (CLL-AHA). Leukemic cells from one patient displayed surface immunoglobulin with heavy and light chain isotypes identical to that of the patient's anti-red blood cell (RBC) antibodies, and the leukemic cells secreted antibodies in vitro with anti-RBC activity. However, in the remaining patients, the leukemic cells displayed surface immunoglobulin with light chain isotypes different from that of the patient's anti-RBC antibodies and secreted antibodies in vitro with no detectable anti-RBC activity. Thus, there are two distinct classes of CLL-AHA patients, differentiated by the presence or absence of an anti-RBC antibody-producing leukemic B cell clone. The apparent heterogeneity in the source of pathogenic anti-RBC antibodies may impact the treatment response of the two classes of CLL-AHA patients.
我们评估了5例同时患有慢性淋巴细胞白血病和自身免疫性溶血性贫血(CLL-AHA)患者白血病B细胞中抗体的特异性。1例患者的白血病细胞表面免疫球蛋白的重链和轻链同种型与该患者的抗红细胞(RBC)抗体相同,并且白血病细胞在体外分泌具有抗RBC活性的抗体。然而,在其余患者中,白血病细胞表面免疫球蛋白的轻链同种型与患者的抗RBC抗体不同,并且在体外分泌的抗体没有可检测到的抗RBC活性。因此,存在两类不同的CLL-AHA患者,通过是否存在产生抗RBC抗体的白血病B细胞克隆来区分。致病性抗RBC抗体来源的明显异质性可能会影响两类CLL-AHA患者的治疗反应。