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基因疗法在范可尼贫血(一种进行性骨髓衰竭综合征)治疗中的应用。

Gene therapy in the treatment of Fanconi anemia, a progressive bone marrow failure syndrome.

作者信息

Williams David A, Croop James, Kelly Patrick

机构信息

Fanconi Anemia Comprehensive Care Center, Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Division of Experimental Hematology, Department of Pediatrics, Cincinnati, OH 45229, USA.

出版信息

Curr Opin Mol Ther. 2005 Oct;7(5):461-6.

Abstract

Fanconi anemia (FA) is a genetic disease characterized by progressive, fatal bone marrow failure, congenital anomalies and predisposition to cancer. Although stem cell transplantation is therapeutic, human leukocyte antigen-identical sibling donors are available to a minority of patients. In murine models and human cells in vitro, gene transfer corrects the FA cellular phenotype of chromosomal breakage in response to DNA-damaging agents, suggesting therapeutic use of gene transfer is possible. However, disease-specific characteristics make application of viral vector technology difficult. Multiple studies are currently underway to develop a gene therapy approach for treating this disease, including phase I trials.

摘要

范可尼贫血(FA)是一种遗传性疾病,其特征为进行性、致命性骨髓衰竭、先天性异常以及易患癌症。尽管干细胞移植具有治疗作用,但只有少数患者能够获得人类白细胞抗原匹配的同胞供体。在小鼠模型和体外培养的人类细胞中,基因转移可纠正FA细胞对DNA损伤剂产生的染色体断裂细胞表型,这表明基因转移可能具有治疗用途。然而,该疾病的特殊特征使得病毒载体技术的应用变得困难。目前正在开展多项研究以开发治疗这种疾病的基因治疗方法,包括I期试验。

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