Saltman D L, Ross J A, Banks R E, Ross F M, Ford A M, Mackie M J
Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh, Scotland.
Blood. 1989 Nov 1;74(6):2062-5.
To establish the clonal origin of a case of concomitant B-cell chronic lymphocytic leukemia (IgM kappa) and multiple myeloma (IGA lambda), we analyzed the immunoglobulin (Ig) gene rearrangements in the patient's blood and bone marrow. Despite the different isotypes, pretreatment investigation of the heavy chain gene (JH) revealed a germline fragment and two identical rearrangements in the blood and marrow. Both kappa and lambda light-chain genes were rearranged in the blood, suggesting peripheral blood lymphocyte involvement in the myeloma. Analysis of the Ig genes after chemotherapy demonstrated no change in the JH or CK rearrangements; however, the lambda genes were now in a germline configuration. Our results suggest that in this patient both chronic lymphocytic leukemia and myeloma originated from the same B-cell progenitor.
为确定一例伴有B细胞慢性淋巴细胞白血病(IgM κ)和多发性骨髓瘤(IgA λ)患者的克隆起源,我们分析了该患者血液和骨髓中的免疫球蛋白(Ig)基因重排。尽管存在不同的同种型,但重链基因(JH)的预处理研究显示在血液和骨髓中有一个种系片段和两个相同的重排。κ和λ轻链基因在血液中均发生重排,提示外周血淋巴细胞参与了骨髓瘤的发生。化疗后Ig基因分析显示JH或CK重排无变化;然而,λ基因现在处于种系构型。我们的结果提示,该患者的慢性淋巴细胞白血病和骨髓瘤均起源于同一个B细胞祖细胞。