Department of Pediatrics and Powell Gene Therapy Center, University of Florida , Gainesville, Florida, USA.
Spark Therapeutics , Philadelphia, Pennsylvania, USA.
Mol Ther Methods Clin Dev. 2016 May 25;3:16034. doi: 10.1038/mtm.2016.34. eCollection 2016.
Therapeutic gene transfer holds the promise of providing lasting therapies and even cures for diseases that were previously untreatable or for which only temporary or suboptimal treatments were available. For some time, clinical gene therapy was characterized by some impressive but rare examples of successes and also several setbacks. However, effective and long-lasting treatments are now being reported from gene therapy trials at an increasing pace. Positive outcomes have been documented for a wide range of genetic diseases (including hematological, immunological, ocular, and neurodegenerative and metabolic disorders) and several types of cancer. Examples include restoration of vision in blind patients, eradication of blood cancers for which all other treatments had failed, correction of hemoglobinopathies and coagulation factor deficiencies, and restoration of the immune system in children born with primary immune deficiency. To date, about 2,000 clinical trials for various diseases have occurred or are in progress, and many more are in the pipeline. Multiple clinical studies reported successful treatments of pediatric patients. Design of gene therapy vectors and their clinical development are advancing rapidly. This article reviews some of the major successes in clinical gene therapy of recent years.
治疗性基因转移有望为以前无法治疗或仅提供暂时或次优治疗的疾病提供持久的治疗甚至治愈。在一段时间内,临床基因治疗的特点是一些令人印象深刻但罕见的成功例子,也有一些挫折。然而,现在越来越多的基因治疗试验报告了有效和持久的治疗方法。广泛的遗传疾病(包括血液、免疫、眼科、神经退行性和代谢紊乱)和多种类型的癌症都有记录到积极的结果。例如,为失明患者恢复视力,消除所有其他治疗方法都失败的血液癌症,纠正血红蛋白病和凝血因子缺乏症,以及为患有原发性免疫缺陷的儿童恢复免疫系统。迄今为止,已经或正在进行针对各种疾病的约 2000 项临床试验,还有更多的临床试验正在筹备中。多项临床研究报告了儿科患者成功治疗的案例。基因治疗载体的设计及其临床开发正在迅速推进。本文综述了近年来临床基因治疗的一些主要成功案例。