遗传增强
治疗性血管生成
缺血
医学
血管生成
基因
生物信息学
病毒载体
离体
基因转移
疾病
体内
生物
严重肢体缺血
外科
血管疾病
动脉疾病
癌症研究
病理
内科学
新生血管
遗传学
重组DNA
作者
V. Z. Tarantul,А. В. Гавриленко
标识
DOI:10.2174/1566523221666210712185742
摘要
Peripheral artery diseases remain a serious public health problem. Although there are many traditional methods for their treatment using conservative therapeutic techniques and surgery, gene therapy is an alternative and potentially more effective treatment option especially for "no-option" patients. This review treats the results of many years of research and application of gene therapy as an example of treatment of patients with critical limb ischemia. Data on successful and unsuccessful attempts to use this technology for treating this disease are presented. Trends in changing the paradigm of approaches to therapeutic angiogenesis are noted: from viral vectors to non-viral vectors, from gene transfer to the whole organism to targeted transfer to cells and tissues, from single-gene use to combination of genes; from DNA therapy to RNA therapy, from in vivo therapy to ex vivo therapy.
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