Testing the safety and efficacy of inhibitory RNA mediated purine analog resistan

测试抑制性 RNA 介导的嘌呤类似物耐药的安全性和有效性

• 批准号: 7837434
• 负责人: CHRISTOPHER C PORTER
• 金额: $ 17.51万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7837434
• 关键词: Adverse effects; Affect; Animals; Autologous; Behavioral; Biological Assay; Blood; Blood Cells; CD34 gene; Cell Transplants; Cells; Chronic Granulomatous Disease; Clinical Research; Clinical Trials; Code; Data; Development; Diamond-Blackfan anemia; Disease; Drug resistance; Effectiveness; Engraftment; Failure; Fanconi Syndrome; Funding Mechanisms; Gene Abnormality; Genes; Genome; Goals; Hematological Disease; Hematopoietic; Hematopoietic stem cells; Hemoglobinopathies; Hereditary Disease; Human; Immunocompromised Host; In Vitro; Inherited; Investigation; Malignant - descriptor; Manuscripts; Measures; Mediating; Methods; Mus; Myelogenous; NOD/SCID mouse; Nature; Pancytopenia; Patients; Pharmaceutical Preparations; Polymerase Chain Reaction; Population; Publishing; RNA; Research; Research Project Grants; Resistance; Retroviridae; Risk; Sickle Cell Anemia; Site; Staging; Subfamily lentivirinae; Syndrome; System; Technology; Testing; Thalassemia; Thioguanine; Toxic effect; Translations; Umbilical Cord Blood; Virus Integration; Wiskott-Aldrich Syndrome; X-Linked Severe Combined Immunodeficiency; Xenograft procedure; gene therapy; genetically modified cells; genotoxicity; human disease; improved; in vivo; lentiviral integration; leukemia; mouse model; nonhuman primate; pre-clinical; preclinical study; prevent; public health relevance; purine analog; research study; safety testing; self-renewal; success; therapeutic gene; tumor

DESCRIPTION (provided by applicant): Gene therapy has long been touted to hold the promise of cure for a variety of congenital diseases. However, gene therapy trials are still small in number and scale due to several problems that have prevented wider application of current technology. Inefficient transduction, poor long term expression, and engraftment failure of ex vivo manipulated cells have slowed the practical advancement of gene therapy. Therefore, the ability to select for or amplify a genetically corrected population of cells from patients with single gene abnormalities might enhance the applicability of gene therapy. Previously investigated strategies for in vivo cell selection have had limited effectiveness and/or require the use of highly toxic medications. We have found that the provision of interfering RNA mediated purine analog resistance (iPAR) allows for efficient in vitro and in vivo selection of lentivirus transduced murine hematopoietic progenitor cells using the purine analog, 6-thioguanine (6TG). We hypothesize that iPAR and purine analogs (iPAR/PA) can be used as a safe and effective means for in vivo selection of autologous, genetically corrected hematopoietic cells to cure human diseases. While we believe that our preliminary data are compelling, substantial pre-clinical studies are essential to determine the applicability of iPAR for use in human patients. With the studies proposed herein, we plan to provide further experimental evidence of the effectiveness of iPAR/PA in hematopoietic cell selection. The specific aims of this project are to 1) determine the effectiveness of iPAR/PA in human hematopoietic progenitor cells and 2) determine the toxicity of lentivirus delivered iPAR and treatment with 6TG as it relates to virus integration into the genome. These aims will be accomplished primarily by using 1) xenografts of human CD34+ umbilical cord blood cells (UCBC) in immunocompromised NOD/SCID mice and 2) identification of lentiviral integration sites by LAM-PCR and sequencing, as well as functional transformation assays including a modified myeloid immortalization assay and a tumor prone mouse model. Positive findings from these studies will justify further investigation of iPAR/PA in larger animals or non-human primates and eventually human patients. A variety of human hematologic diseases would benefit from this strategy of in vivo cell selection, including, but not limited to congenital bone marrow failure syndromes (Fanconi and Diamond-Blackfan anemias), chronic granulomatous disease, Wiscott-Aldrich syndrome, hemoglobinopathies (sickle cell disease, thalassemias), and even hemophilias. PUBLIC HEALTH RELEVANCE: The goal of these experiments is to improve current efforts to cure genetic diseases of the blood system. The strategy involves providing drug resistance to the cells that have been genetically corrected, followed by selection of these cells within the body using a medication that may be safer than others that have been previously studied. This strategy could be applied to a variety of human diseases such as bone marrow failure syndromes, hemoglobinopathies, and hemophilias.

描述(申请人提供)：长期以来，基因疗法一直被吹捧为治愈各种先天性疾病的希望。然而，由于一些问题阻碍了当前技术的更广泛应用，基因治疗试验的数量和规模仍然很小。体外操控细胞转导效率低、长期表达差、植入失败等因素阻碍了基因治疗的实用化进程。因此，从单基因异常患者中选择或扩增经过基因纠正的细胞群体的能力可能会增强基因治疗的适用性。以前研究的体内细胞选择策略的有效性有限，和/或需要使用剧毒药物。我们发现，干扰RNA介导的嘌呤类似物抵抗(IPar)的提供允许使用嘌呤类似物6-硫代鸟嘌呤(6TG)在体外和体内高效地选择慢病毒转导的小鼠造血祖细胞。我们推测，iPar和嘌呤类似物(iPar/PA)可以作为一种安全和有效的手段，用于体内选择自体的、经过基因修正的造血细胞来治疗人类疾病。虽然我们相信我们的初步数据是令人信服的，但大量的临床前研究对于确定iPar是否适用于人类患者至关重要。通过本文提出的研究，我们计划为iPar/PA在造血细胞选择中的有效性提供进一步的实验证据。本项目的具体目的是：1)确定iPar/PA在人造血祖细胞中的有效性；2)确定慢病毒携带的iPar和6TG治疗的毒性，因为它与病毒整合到基因组中有关。这些目标将主要通过1)将人CD34+脐血细胞(UCBC)移植到免疫低下的NOD/SCID小鼠中，2)通过LAM-PCR和测序鉴定慢病毒整合位点，以及功能转化分析，包括改良的髓系永生化试验和易患肿瘤的小鼠模型来实现。这些研究的积极发现将证明在更大的动物或非人类灵长类动物以及最终的人类患者中进一步研究iPar/PA是合理的。多种人类血液疾病将从体内细胞选择策略中受益，包括但不限于先天性骨髓衰竭综合征(Fanconi和Diamond-Blackfan贫血)、慢性肉芽肿疾病、Wiscott-Aldrich综合征、血红蛋白疾病(镰状细胞疾病、地中海贫血)，甚至血友病。公共卫生相关性：这些实验的目标是改进目前治愈血液系统遗传疾病的努力。该策略包括为经过基因纠正的细胞提供抗药性，然后使用一种可能比之前研究的其他药物更安全的药物在体内选择这些细胞。这一策略可以应用于多种人类疾病，如骨髓衰竭综合征、血红蛋白疾病和血友病。