Gordon J, Aman P, Mellstedt H, Biberfeld P, Klein G
Leuk Res. 1983;7(2):133-8. doi: 10.1016/0145-2126(83)90003-6.
Neoplastic populations from three cases of chronic lymphocytic leukaemia (CLL) which had features consistent with a maturation arrest at the 'small pre-B' stage are described. The cells were small and rounded with a scanty cytoplasm and stained for mu heavy chains but not light chains intracellularly while surface immunoglobulin (SmIg) was either undetectable or expressed sparsely on a minority of cells. Other features included the weak expression of B1, a lack of B2, an absence of the common acute lymphoblastic leukaemia antigen (cALLA), the presence of Ia and a variable expression of the receptors for Fc gamma and C3. Successful induction of in vitro differentiation in all three of the cases allowed the identification of a sequence of events whereby cells initially containing isolated mu heavy chains in their cytoplasm, on commencing light chain synthesis, begin to express stable SmIgM while surplus light chain is secreted without any association with the heavy chain. Although this is followed ultimately by the secretion of intact Ig effector molecules, the export of surplus light chains is apparently maintained throughout the developmental sequence. These findings are discussed with particular emphasis on their relation to normal B-cell maturation.
描述了3例慢性淋巴细胞白血病(CLL)的肿瘤细胞群,其特征与“小前B”阶段的成熟停滞一致。细胞小而圆,细胞质稀少,胞内μ重链染色阳性,但轻链染色阴性,而表面免疫球蛋白(SmIg)要么检测不到,要么在少数细胞上稀疏表达。其他特征包括B1表达较弱、缺乏B2、不存在普通急性淋巴细胞白血病抗原(cALLA)、存在Ia以及Fcγ和C3受体的可变表达。在所有3例病例中成功诱导体外分化,从而确定了一系列事件,即最初细胞质中含有分离的μ重链的细胞,在开始轻链合成时,开始表达稳定的SmIgM,而多余的轻链则在不与重链结合的情况下分泌。尽管最终会分泌完整的Ig效应分子,但多余轻链的输出显然在整个发育过程中持续存在。对这些发现进行了讨论,特别强调了它们与正常B细胞成熟的关系。