Brenner M K
St Jude Children's Research Hospital, Cell and Gene Therapy Program, Memphis, TN 38105-2794, USA.
Ann Med. 1996 Dec;28(6):491-7. doi: 10.3109/07853899608999113.
Although gene transfer was first suggested to treat inherited monogenic disorders, at present most clinical protocols are intended to treat patients with malignant disease. Although current vector technologies profoundly limit the potential therapeutic applications of gene transfer, the technique is already being successfully used to complement longer established therapies. This article reviews current and forthcoming applications of gene transfer to treat haematological malignancies.
尽管基因转移最初被提出用于治疗遗传性单基因疾病,但目前大多数临床方案旨在治疗恶性疾病患者。虽然当前的载体技术极大地限制了基因转移的潜在治疗应用,但该技术已成功用于补充更成熟的疗法。本文综述了基因转移在治疗血液系统恶性肿瘤方面的当前及未来应用。