Horák Jan, Nalos Lukáš, Martínková Vendula, Beneš Jan, Štengl Milan, Matějovič Martin
1st Medical Department, Faculty of Medicine in Pilsen, Charles University, Prague, Czech Republic.
Experimental Intensive Care Unit, Biomedical Centre, Faculty of Medicine in Plzen, Charles University, Alej Svobody 1655/76, Plzen, Czech Republic.
Stem Cells Int. 2017;2017:7304121. doi: 10.1155/2017/7304121. Epub 2017 Sep 14.
Sepsis, newly defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection, is the most common cause of death in ICUs and one of the principal causes of death worldwide. Although substantial progress has been made in the understanding of fundamental mechanisms of sepsis, translation of these advances into clinically effective therapies has been disappointing. Given the extreme complexity of sepsis pathogenesis, the paradigm "one disease, one drug" is obviously flawed and combinations of multiple targets that involve early immunomodulation and cellular protection are needed. In this context, the immune-reprogramming properties of cell-based therapy using mesenchymal stem cells (MSC) represent an emerging therapeutic strategy in sepsis and associated organ dysfunction. This article provides an update of the current knowledge regarding MSC in preclinical models of sepsis and sepsis-induced acute kidney injury. Recommendations for further translational research in this field are discussed.
脓毒症,新近被定义为由宿主对感染的失调反应所导致的危及生命的器官功能障碍,是重症监护病房(ICU)中最常见的死亡原因,也是全球主要死亡原因之一。尽管在脓毒症基本机制的理解方面已取得重大进展,但将这些进展转化为临床有效治疗方法的成果却令人失望。鉴于脓毒症发病机制极其复杂,“一种疾病,一种药物”的模式显然存在缺陷,需要涉及早期免疫调节和细胞保护的多个靶点的联合治疗。在此背景下,使用间充质干细胞(MSC)的细胞疗法的免疫重编程特性代表了脓毒症及相关器官功能障碍的一种新兴治疗策略。本文提供了关于MSC在脓毒症临床前模型和脓毒症诱导的急性肾损伤方面的当前知识的更新。并讨论了该领域进一步转化研究的建议。