Department of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.
Am J Hematol. 2019 Jan;94(1):93-102. doi: 10.1002/ajh.25337. Epub 2018 Nov 25.
Adult B-lymphoblastic leukemia (B-ALL) is a hematological malignancy characterized by genetic heterogeneity. Despite successful remission induction with classical chemotherapeutics and novel targeted agents, enduring remission is often hampered by disease relapse due to outgrowth of a pre-existing subclone resistant against the treatment. In this study, we show that small glycophosphatidylinositol (GPI)-anchor deficient CD52-negative B-cell populations are frequently present already at diagnosis in B-ALL patients, but not in patients suffering from other B-cell malignancies. We demonstrate that the GPI-anchor negative phenotype results from loss of mRNA expression of the PIGH gene, which is involved in the first step of GPI-anchor synthesis. Loss of PIGH mRNA expression within these B-ALL cells follows epigenetic silencing rather than gene mutation or deletion. The coinciding loss of CD52 membrane expression may contribute to the development of resistance to alemtuzumab (ALM) treatment in B-ALL patients resulting in the outgrowth of CD52-negative escape variants. Additional treatment with 5-aza-2'-deoxycytidine may restore expression of CD52 and revert ALM resistance.
成人 B 淋巴细胞白血病(B-ALL)是一种以遗传异质性为特征的血液系统恶性肿瘤。尽管通过经典化疗药物和新型靶向药物成功诱导缓解,但由于先前存在的对治疗有抗性的亚克隆的生长,疾病复发常常阻碍持久缓解。在这项研究中,我们表明,在 B-ALL 患者中,在诊断时已经经常存在小糖基磷脂酰肌醇(GPI)锚缺失的 CD52 阴性 B 细胞群体,但在患有其他 B 细胞恶性肿瘤的患者中不存在。我们证明,GPI-锚缺失表型是由于 PIGH 基因的 mRNA 表达缺失所致,该基因参与 GPI-锚合成的第一步。这些 B-ALL 细胞中 PIGH mRNA 表达的缺失遵循表观遗传沉默而不是基因突变或缺失。CD52 膜表达的同时缺失可能导致 B-ALL 患者对阿仑单抗(ALM)治疗产生耐药性,从而产生 CD52 阴性逃逸变体的生长。用 5-氮杂-2'-脱氧胞苷进行额外治疗可能恢复 CD52 的表达并逆转 ALM 耐药性。