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肿瘤坏死因子相关凋亡诱导配体(TRAIL)可改善固有免疫反应并提高多微生物脓毒症小鼠的存活率。

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) improves the innate immune response and enhances survival in murine polymicrobial sepsis.

机构信息

Department of Surgery, Ernst-Moritz-Arndt University Greifswald, Germany.

出版信息

Crit Care Med. 2010 Nov;38(11):2169-74. doi: 10.1097/CCM.0b013e3181eedaa8.

Abstract

OBJECTIVE

To investigate the role of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) in postoperative polymicrobial abdominal sepsis.Sepsis is the leading cause of death among critically ill surgical patients. TRAIL is commonly known as an apoptosis-inducing agent in cancer cells. It also plays an important role in the regulation of inflammatory reactions. The role of TRAIL in polymicrobial sepsis is still unclear.

DESIGN

Experimental animal model.

SETTING

University laboratory.

SUBJECTS

C57BL/6 mice.

INTERVENTIONS

Colon ascendens stent peritonitis (CASP) was induced in female mice. One hour, 24 hrs, and 48 hrs after induction of CASP, murine recombinant TRAIL was given intravenously.

MEASUREMENTS AND MAIN RESULTS

This study demonstrates a protective effect of TRAIL in CASP, an experimental model of murine polymicrobial sepsis. Intravenous administration of recombinant TRAIL to mice after CASP induction led to highly significantly prolonged survival. The migration of effector cells into the peritoneal cavity was strongly enhanced. Consequently, TRAIL-treated mice eliminated bacteria significantly better from the peritoneal cavity, the source of infection. Systemic spread of gut bacteria was also reduced by several orders of magnitude. As a result of the reduced systemic spread of bacteria, the accumulation of neutrophils within the spleen and mesenteric lymph nodes was strongly decreased.

CONCLUSION

TRAIL-treated mice are highly protected from abdominal sepsis. Because diagnosis and therapy are frequently delayed in human sepsis, it is remarkable that TRAIL is effective when given via a therapeutic approach. Therefore, this study suggests a therapeutic potential for TRAIL in human sepsis. This should be addressed in future trials.

摘要

目的

探讨肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)在术后多微生物性腹脓毒症中的作用。脓毒症是危重症外科患者死亡的主要原因。TRAIL 通常被认为是癌细胞凋亡诱导剂。它在炎症反应的调节中也起着重要作用。TRAIL 在多微生物性脓毒症中的作用尚不清楚。

设计

实验动物模型。

地点

大学实验室。

研究对象

C57BL/6 小鼠。

干预

诱导雌性小鼠升结肠支架腹膜炎(CASP)。在诱导 CASP 后 1 小时、24 小时和 48 小时,给予小鼠重组 TRAIL 静脉内给药。

测量和主要结果

本研究表明 TRAIL 在 CASP 中具有保护作用,CASP 是一种多微生物性脓毒症的实验模型。在 CASP 诱导后给予重组 TRAIL 静脉内给药可显著延长小鼠的存活时间。效应细胞向腹腔内的迁移明显增强。因此,TRAIL 治疗的小鼠从腹腔(感染源)中清除细菌的效果明显更好。肠道细菌的全身扩散也减少了几个数量级。由于细菌全身扩散减少,脾和肠系膜淋巴结内中性粒细胞的积聚也明显减少。

结论

TRAIL 治疗的小鼠对腹脓毒症有高度保护作用。由于人类脓毒症的诊断和治疗经常延迟,TRAIL 在治疗方法中有效是值得注意的。因此,本研究提示 TRAIL 在人类脓毒症中有治疗潜力。这应在未来的试验中得到解决。

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