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首页> 外文期刊>Intensive care medicine >Transient Bcl-2 gene down-expression in circulating mononuclear cells of severe sepsis patients who died despite appropriate intensive care.
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Transient Bcl-2 gene down-expression in circulating mononuclear cells of severe sepsis patients who died despite appropriate intensive care.

机译:重度脓毒症患者的循环单核细胞中瞬时Bcl-2基因表达下调,尽管经过适当的重症监护仍然死亡。

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摘要

OBJECTIVE: To assess the levels of expression of the antiapoptotic gene Bcl-2 and the proapoptotic gene Bax in circulating mononuclear cells (CMNC) harvested during the course of severe sepsis (SS) in formerly non-immunocompromised patients undergoing hospital-acquired infection, in parallel to cytokine levels. DESIGN: Prospective study. SETTING: Intensive care unit. PARTICIPANTS: A total of 24 patients without immunodeficiency undergoing standard goal-directed therapy for nosocomial SS, 10 critically ill patients without sepsis, and 10 healthy controls. INTERVENTIONS: Blood was collected before infection and within 12 h, 1, 3 and 7 days after fever onset, to determine plasma concentrations of IL-6, IL-10, TNF-alpha, C-reactive protein, whole blood cell counts, lymphocyte subsets, annexin V labelling for apoptosis, and Bax and Bcl-2 relative RNA expression by real-time polymerase chain reaction. RESULTS: SS patients displayed increased cytokine concentrations, TNF-alpha being significantly increased atfull-blown sepsis. Within 12 h after onset of infection, lymphocyte counts were lower in SS patients than in critically ill controls ( p=0.001), and this phenomenon was marked in CD4+ and CD8+ subsets ( p<0.001). This was associated with enhanced apoptosis in CMNC (15.7+/-8.7% vs 3.4+/-2.1%, p<0.001) and a significant down-expression of the Bcl-2 gene throughout the study ( p<0.05). In contrast, the expression of Bax did not change significantly. Within 12 h of fever onset, non-survivors expressed a 10-fold down-expression of Bcl-2 when compared to survivors ( p<0.001). CONCLUSIONS: An early transient down-expression of the gene Bcl-2 occurred in CMNC harvested from SS patients who died despite intensive care. In contrast, the expression of the gene Bax did not change significantly.
机译:目的:评估原发于非免疫功能低下的原发性医院感染患者在严重脓毒症(SS)过程中收集的循环单核细胞(CMNC)中抗凋亡基因Bcl-2和促凋亡基因Bax的表达水平。与细胞因子水平平行。设计:前瞻性研究。地点:重症监护室。参与者:共有24例无免疫缺陷的患者接受了针对医院SS的标准目标导向疗法,10例无败血症的危重患者和10例健康对照。干预措施:在感染前以及发烧后12小时,1、3和7天内收集血液,以确定血浆中IL-6,IL-10,TNF-α,C反应蛋白的浓度,全血细胞计数,淋巴细胞亚组,膜联蛋白V标记凋亡,以及通过实时聚合酶链反应进行Bax和Bcl-2相对RNA表达。结果:SS患者显示出增加的细胞因子浓度,TNF-α在成熟脓毒症中显着增加。在感染发作后的12小时内,SS患者的淋巴细胞计数低于危重对照组(p = 0.001),并且该现象在CD4 +和CD8 +亚群中明显(p <0.001)。在整个研究过程中,这与CMNC细胞凋亡的增加有关(15.7 +/- 8.7%对3.4 +/- 2.1%,p <0.001)以及Bcl-2基因的显着下调(p <0.05)。相反,Bax的表达没有明显变化。在发热开始后的12小时内,与幸存者相比,非幸存者的Bcl-2表达下调了10倍(p <0.001)。结论:从重症监护病房死亡的SS患者收集的CMNC中,出现了Bcl-2基因的早期短暂表达。相反,基因Bax的表达没有明显改变。

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