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脓毒症亚表型:弥合脓毒症治疗策略的差距

Sepsis subphenotypes: bridging the gaps in sepsis treatment strategies.

作者信息

Zhang Xue, Zhang Wei, Zhang Huan, Liao Xuelian

机构信息

Department of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

Institute of Critical Care Medicine, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Front Immunol. 2025 Feb 6;16:1546474. doi: 10.3389/fimmu.2025.1546474. eCollection 2025.

DOI:10.3389/fimmu.2025.1546474
PMID:40013154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11862915/
Abstract

Sepsis, a heterogeneous illness produced by a dysregulated host response to infection, remains a severe mortality risk. Recent discoveries in sepsis research have stressed phenotyping as a feasible strategy for tackling heterogeneity and enhancing therapy precision. Sepsis phenotyping has moved from traditional stratifications based on severity and prognosis to dynamic, phenotype-driven therapeutic options. This review covers recent progress in connecting sepsis subgroups to personalized treatments, with a focus on phenotype-based therapeutic predictions and decision-support systems. Despite ongoing challenges, such as standardizing phenotyping frameworks and incorporating findings into clinical practice, this topic has enormous promise. By investigating phenotypic variation in therapy responses, we hope to uncover new biomarkers and phenotype-driven therapeutic solutions, laying the groundwork for more effective therapies and, ultimately improving patient outcomes.

摘要

脓毒症是宿主对感染的反应失调所导致的一种异质性疾病,仍然是严重的死亡风险。脓毒症研究的最新发现强调表型分型是应对异质性和提高治疗精准度的可行策略。脓毒症表型分型已从基于严重程度和预后的传统分层转向动态的、由表型驱动的治疗选择。本综述涵盖了将脓毒症亚组与个性化治疗相联系的最新进展,重点关注基于表型的治疗预测和决策支持系统。尽管存在持续的挑战,如使表型分型框架标准化以及将研究结果纳入临床实践,但该主题具有巨大的前景。通过研究治疗反应中的表型变异,我们希望发现新的生物标志物和由表型驱动的治疗方案,为更有效的治疗奠定基础,并最终改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/e0f5d3bcadc8/fimmu-16-1546474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/9c09ce503b21/fimmu-16-1546474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/34958bc9d309/fimmu-16-1546474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/79196e8f7c2c/fimmu-16-1546474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/e0f5d3bcadc8/fimmu-16-1546474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/9c09ce503b21/fimmu-16-1546474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/34958bc9d309/fimmu-16-1546474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/79196e8f7c2c/fimmu-16-1546474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/11862915/e0f5d3bcadc8/fimmu-16-1546474-g004.jpg

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本文引用的文献

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Temporal Transitions of the Hyperinflammatory and Hypoinflammatory Phenotypes in Critical Illness.危重症中高炎症和低炎症表型的时间转变
Am J Respir Crit Care Med. 2025 Mar;211(3):347-356. doi: 10.1164/rccm.202406-1241OC.
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Clinical phenotyping of septic shock with latent profile analysis: A retrospective multicenter study.基于潜在剖面分析的感染性休克临床表型分析:一项回顾性多中心研究
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Identifying septic shock subgroups to tailor fluid strategies through multi-omics integration.
脓毒症相关急性肾损伤中DNA甲基化的分子见解及临床意义:一项叙述性综述
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Distinct immune profiles and clinical outcomes in sepsis subphenotypes based on temperature trajectories.基于体温轨迹的脓毒症亚表型的不同免疫特征和临床结局。
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Unraveling the impact of therapeutic drug monitoring via machine learning for patients with sepsis.通过机器学习解析脓毒症患者治疗药物监测的影响。
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Endothelial dysfunction: Pathophysiology and therapeutic targets for sepsis-induced multiple organ dysfunction syndrome.内皮功能障碍:脓毒症诱导的多器官功能障碍综合征的病理生理学和治疗靶点。
Biomed Pharmacother. 2024 Sep;178:117180. doi: 10.1016/j.biopha.2024.117180. Epub 2024 Jul 27.
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From Molecular Mechanisms to Clinical Therapy: Understanding Sepsis-Induced Multiple Organ Dysfunction.从分子机制到临床治疗:了解脓毒症引起的多器官功能障碍。
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