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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Nucleic-acid based gene therapy approaches for sepsis
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Nucleic-acid based gene therapy approaches for sepsis

机译:基于核酸的基于核酸基因治疗方法

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Despite advances in overall medical care, sepsis and its sequelae continue to be an embarrassing clinical entity with an unacceptably high mortality rate. The central reason for high morbidity and high mortality of sepsis and its sequelae is the lack of an effective treatment. Previous clinical trials have largely failed to identify an effective therapeutic target to improve clinical outcomes in sepsis. Thus, the key goal favoring the outcome of septic patients is to devise innovative and evolutionary therapeutic strategies. Gene therapy can be considered as one of the most promising novel therapeutic approaches for nasty disorders. Since a number of transcription factors, such as nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1), play a pivotal role in the pathophysiology of sepsis that can be characterized by the induction of multiple genes and their products, sepsis may be regarded as a gene-related disorder and gene therapy may be considered a promising novel therapeutic approach for treatment of sepsis. In this review article, we provide an up-to-date summary of the gene-targeting approaches, which have been developed in animal models of sepsis. Our review sheds light on the molecular basis of sepsis pathology for the development of novel gene therapy approaches and leads to the conclusion that future research efforts may fully take into account gene therapy for the treatment of sepsis.
机译:尽管在整体医疗保健,脓毒症及其后遗症的进展仍然是一个令人尴尬的临床实体不可接受的高死亡率。高发病率和败血症的死亡率高及其后遗症的核心原因是缺乏有效的治疗手段。上一页临床试验​​已经在很大程度上未能确定一个有效的治疗靶点改善败血症的临床结果。因此,有利于脓毒症患者的预后的主要目标是设计创新和进化的治疗策略。基因治疗可被认为是最有前途的新的治疗的一个方法为讨厌病症。因为许多转录因子,如核因子-κB(NF-κB的)和激活蛋白-1(AP-1),播放在脓毒症病理生理学可被多个基因的诱导来表征了关键作用和他们的产品,败血症可视为一个基因相关的疾病及基因治疗可以考虑用于治疗脓毒症的有前途的新的治疗方法。在这篇综述文章中,我们所提供的基因靶向技术,已在败血症的动物模型被开发的最高最新总结。我们的审查阐明了败血症病变的新型基因疗法的发展的分子基础方法和得出的结论,今后的研究工作可以充分考虑到基因治疗脓毒症的治疗。

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