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脓毒症相关性肝损伤:机制与潜在治疗靶点。

Sepsis-associated liver injury: Mechanisms and potential therapeutic targets.

机构信息

Department of Infectious Diseases, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China.

出版信息

World J Gastroenterol. 2024 Nov 14;30(42):4518-4522. doi: 10.3748/wjg.v30.i42.4518.

Abstract

In this editorial, we examined a recent article in the that focused on sepsis-associated liver injury (SLI) and its treatment. SLI is a serious complication of sepsis, primarily caused by microcirculatory disturbances, the gut-liver axis, and inflammatory responses. Specific treatment recommendations for SLI are lacking. The gut-liver axis represents a potential therapeutic target, with metformin showing promise in modulating the gut microbiome and enhancing intestinal barrier function. Although immunomodulatory therapies are being explored, anti-tumor necrosis factor agents and interleukin-1 receptor antagonists have not demonstrated significant clinical benefits. Statins may reduce liver inflammation and prevent injury in sepsis, but their clinical application is limited. Reduced D-related human leucocyte antigen expression on monocytes and lymphocytes suggests immune suppression in patients, indicating that corticosteroids could reverse clinical deterioration in severe infections and address adrenal cortical insufficiency. Current large-scale studies on glucocorticoid therapy for sepsis have yielded mixed results, likely due to inadequate assessment of the immune status of the host. Future research should prioritize the development of personalized immunotherapy tailored to patients' immune profiles, focusing on identifying novel indicators of immune status and advancing immunomodulatory targets and therapeutics for septic patients.

摘要

在这篇社论中,我们检查了最近在[杂志名称]上发表的一篇文章,该文章聚焦于脓毒症相关肝损伤(SLI)及其治疗。SLI 是脓毒症的严重并发症,主要由微循环紊乱、肠-肝轴和炎症反应引起。目前缺乏针对 SLI 的具体治疗建议。肠-肝轴是一个潜在的治疗靶点,二甲双胍在调节肠道微生物群和增强肠道屏障功能方面显示出前景。虽然正在探索免疫调节疗法,但抗肿瘤坏死因子制剂和白细胞介素-1 受体拮抗剂并未显示出显著的临床获益。他汀类药物可能减少脓毒症中的肝脏炎症和损伤,但它们的临床应用受到限制。单核细胞和淋巴细胞上 D 相关人类白细胞抗原表达减少表明患者存在免疫抑制,这表明皮质类固醇可能逆转严重感染的临床恶化,并解决肾上腺皮质功能不全。目前关于脓毒症皮质类固醇治疗的大型研究结果喜忧参半,这可能是由于宿主免疫状态评估不足所致。未来的研究应优先制定针对患者免疫谱的个性化免疫疗法,重点是确定新的免疫状态指标,并推进脓毒症患者的免疫调节靶点和治疗方法。

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