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治疗中的基因转移技术:当前应用与未来目标

Gene transfer technology in therapy: current applications and future goals.

作者信息

Romano G, Pacilio C, Giordano A

机构信息

Kimmel Cancer Center, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Stem Cells. 1999;17(4):191-202. doi: 10.1002/stem.170191.

Abstract

Gene therapy has attracted much interest since the first submissions of phase I clinical trials in the early 1990s, for the treatment of inherited genetic diseases. Preliminary results were very encouraging and prompted many investigators to submit protocols for phase I and phase II clinical trials for the treatment of inherited genetic diseases and cancer. The possible application of gene transfer technology to treat AIDS, cardiopathies, and neurologic diseases is under evaluation. Some viral vectors have already been used to deliver HIV-1 subunits to immunize volunteers who are participating in the AIDS vaccine programs in the USA. However, gene delivery systems still need to be optimized in order to achieve effective therapeutic interventions. The purpose of this review is to summarize the latest achievements in improving gene delivery systems, their current application in preclinical studies and in therapy, and the most pressing issues that must be addressed in the area of vector design.

摘要

自20世纪90年代初首次提交I期临床试验申请用于治疗遗传性疾病以来,基因治疗已引起了广泛关注。初步结果非常令人鼓舞,并促使许多研究人员提交了用于治疗遗传性疾病和癌症的I期和II期临床试验方案。基因转移技术在治疗艾滋病、心脏病和神经系统疾病方面的潜在应用正在评估中。一些病毒载体已被用于递送HIV-1亚基,以免疫参与美国艾滋病疫苗项目的志愿者。然而,为了实现有效的治疗干预,基因递送系统仍需优化。本综述的目的是总结在改进基因递送系统方面的最新成果、它们在临床前研究和治疗中的当前应用,以及载体设计领域必须解决的最紧迫问题。

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