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Ferret and Pig Models of Cystic Fibrosis: Prospects and Promise for Gene Therapy

机译:雪貂和猪囊性纤维化的模型:基因治疗的前景和承诺

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摘要

Large animal models of genetic diseases are rapidly becoming integral to biomedical research as technologies to manipulate the mammalian genome improve. The creation of cystic fibrosis (CF) ferrets and pigs is an example of such progress in animal modeling, with the disease phenotypes in the ferret and pig models more reflective of human CF disease than mouse models. The ferret and pig CF models also provide unique opportunities to develop and assess the effectiveness of gene and cell therapies to treat affected organs. In this review, we examine the organ disease phenotypes in these new CF models and the opportunities to test gene therapies at various stages of disease progression in affected organs. We then discuss the progress in developing recom-binant replication-defective adenoviral, adeno-associated viral, and lentiviral vectors to target genes to the lung and pancreas in ferrets and pigs, the two most affected organs in CF. Through this review, we hope to convey the potential of these new animal models for developing CF gene and cell therapies.
机译:大的遗传疾病的动物模型迅速成为不可或缺的生物医学研究作为哺乳动物的技术操作基因组得到改善。(CF)雪貂和猪是这样的一个例子进步在动物模型中,疾病表型的雪貂和猪模型反映人类CF疾病小鼠模型。雪貂和猪的CF模型还提供了独一无二的开发和评估的机会基因和细胞疗法治疗的有效性受影响的器官。在这些新的CF模型器官疾病表型和测试基因疗法的机会疾病进展的不同阶段的影响器官。发展recom-binant replication-defectiveadenoviral,腺相关病毒目标基因的慢病毒载体的肺在雪貂和猪胰腺,两大部分受影响的器官在CF。通过本文,我们希望传达的潜力这些新的动物模型开发CF基因和细胞治疗。

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