Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6076, USA.
Blood. 2010 Jun 3;115(22):4356-66. doi: 10.1182/blood-2009-12-257352. Epub 2010 Mar 12.
X-linked severe-combined immunodeficiency (SCID-X1) has been treated by therapeutic gene transfer using gammaretroviral vectors, but insertional activation of proto-oncogenes contributed to leukemia in some patients. Here we report a longitudinal study of gene-corrected progenitor cell populations from 8 patients using 454 pyrosequencing to map vector integration sites, and extensive resampling to allow quantification of clonal abundance. The number of transduced cells infused into patients initially predicted the subsequent diversity of circulating cells. A capture-recapture analysis was used to estimate the size of the gene-corrected cell pool, revealing that less than 1/100th of the infused cells had long-term repopulating activity. Integration sites were clustered even at early time points, often near genes involved in growth control, and several patients harbored expanded cell clones with vectors integrated near the cancer-implicated genes CCND2 and HMGA2, but remain healthy. Integration site tracking also documented that chemotherapy for adverse events resulted in successful control. The longitudinal analysis emphasizes that key features of transduced cell populations--including diversity, integration site clustering, and expansion of some clones--were established early after transplantation. The approaches to sequencing and bioinformatics analysis reported here should be widely useful in assessing the outcome of gene therapy trials.
X 连锁重症联合免疫缺陷(SCID-X1)已通过使用γ逆转录病毒载体的治疗性基因转移进行治疗,但原癌基因的插入激活导致一些患者发生白血病。在此,我们通过 454 焦磷酸测序对 8 名患者的基因校正祖细胞群进行了纵向研究,以绘制载体整合位点图谱,并进行广泛的重采样以定量克隆丰度。输注到患者体内的转导细胞数量最初预测了循环细胞的后续多样性。使用捕获-再捕获分析来估计基因校正细胞池的大小,结果表明,输注的细胞中只有不到 1/100 具有长期的再生活性。整合位点甚至在早期就聚集在一起,通常靠近参与生长控制的基因,并且一些患者带有整合在癌症相关基因 CCND2 和 HMGA2 附近的载体的扩展细胞克隆,但仍保持健康。整合位点跟踪还记录了因不良事件进行的化疗已成功控制了病情。纵向分析强调,转导细胞群的关键特征——包括多样性、整合位点聚类和某些克隆的扩增——在移植后早期就已确立。这里报告的测序和生物信息学分析方法应该广泛用于评估基因治疗试验的结果。