San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Paediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Nat Commun. 2024 Apr 30;15(1):3662. doi: 10.1038/s41467-024-47866-5.
Hematopoietic stem cell gene therapy (GT) using a γ-retroviral vector (γ-RV) is an effective treatment for Severe Combined Immunodeficiency due to Adenosine Deaminase deficiency. Here, we describe a case of GT-related T-cell acute lymphoblastic leukemia (T-ALL) that developed 4.7 years after treatment. The patient underwent chemotherapy and haploidentical transplantation and is currently in remission. Blast cells contain a single vector insertion activating the LIM-only protein 2 (LMO2) proto-oncogene, confirmed by physical interaction, and low Adenosine Deaminase (ADA) activity resulting from methylation of viral promoter. The insertion is detected years before T-ALL in multiple lineages, suggesting that further hits occurred in a thymic progenitor. Blast cells contain known and novel somatic mutations as well as germline mutations which may have contributed to transformation. Before T-ALL onset, the insertion profile is similar to those of other ADA-deficient patients. The limited incidence of vector-related adverse events in ADA-deficiency compared to other γ-RV GT trials could be explained by differences in transgenes, background disease and patient's specific factors.
采用γ-逆转录病毒载体(γ-RV)的造血干细胞基因治疗(GT)是治疗由于腺苷脱氨酶缺乏引起的严重联合免疫缺陷症的有效方法。在这里,我们描述了一例治疗后 4.7 年发生的 GT 相关 T 细胞急性淋巴细胞白血病(T-ALL)的病例。患者接受了化疗和半相合移植,目前处于缓解期。白血病细胞包含一个激活 LIM 仅蛋白 2(LMO2)原癌基因的单一载体插入,这是通过物理相互作用证实的,并且由于病毒启动子的甲基化导致腺苷脱氨酶(ADA)活性降低。该插入在 T-ALL 发生前多年在多个谱系中被检测到,提示在胸腺祖细胞中发生了进一步的打击。白血病细胞包含已知和新的体细胞突变以及种系突变,这些突变可能促成了转化。在 T-ALL 发病前,插入谱与其他 ADA 缺陷患者的插入谱相似。与其他 γ-RV GT 试验相比,ADA 缺陷患者中与载体相关的不良事件发生率较低,这可以通过转染基因、背景疾病和患者特定因素的差异来解释。