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Stem Cell Gene Transfer: Insights into Integration and Hematopoiesis from Primate Genetic Marking Studies

机译:干细胞基因转移:与灵长类动物遗传标记研究中的整合和血液缺陷见解

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Genetic marking strategies in the nonhuman primate model have elucidated a number of principles with relevance to implementation of clinical stem cell therapies, including the lineage potential, number, and life span of hematopoietic stem and progenitor cells. The recent occurrence of leukemias likely related to insertional activation of a proto-oncogene in two patients with X-severe combined immunodeficiency (SCID) syndromes treated with CD34~+ cells transduced with retroviral vectors expressing the corrective common γ cytokine receptor gene has refocused attention on the issue of retroviral integration. We have analyzed >1500 independent insertions from rhesus macaques transplanted with CD34~+ cells transduced with either MLV or SIV vectors. Of these, 46 rhesus macaques followed long term have not had progression to leukemia, abnormal hematopoiesis, or clonal hematopoiesis. However, the pattern of both MLV and SIV integrants in cells of these animals was found to be highly nonrandom, with a propensity for insertions of both vectors within genes: for MLV particularly near the transcription start site, and for SIV particularly in gene-dense regions.
机译:非人类灵长类动物模型中的遗传标记策略阐述了许多与临床干细胞疗法的实施相关的原则,包括血液生成茎和祖细胞的谱系潜力,数量和寿命。最近发生的白血病可能与用CD34〜+细胞治疗的两名X严重组合免疫缺陷(SCID)综合征(SCID)综合征患者的插入激活,所述CD34〜+细胞转导的逆转录病毒载体的逆转录常见的γ细胞因子受体基因转移已重新注释逆转录病毒整合问题。我们已经分析了> 1500从移植的恒河猴的独立插入,用MLV或SIV载体转导的CD34〜+细胞。其中,46个恒河猴,长期患有白血病,异常血小病或克隆血液血液的进展。然而,发现这些动物细胞中的MLV和SIV整合体的模式是高度的非谐振,其用于在基因内插入两个载体的倾向:对于MLV,特别是在转录起始位点附近,特别是在基因密集中的SIV。地区。

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