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揭示脓毒症的研究进展:发病机制、精准干预及临床展望

Unveiling the research advances of sepsis: pathogenesis, precise intervention and clinical perspective.

作者信息

Cheng Lingxia, Cao Yu, Liu Shihao, Lv Lukai, Zhang Jianjun, Bao Ji, Wang Guan, Xu Ping

机构信息

Emergency Department, Zigong Fourth People's Hospital, Sichuan, China.

State Key Laboratory of Biotherapy and Cancer Center, Collaborative Innovation Center of Biotherapy, West China Hospital, Sichuan University, Sichuan, China.

出版信息

Int J Surg. 2025 Jun 23;111(9):6260-89. doi: 10.1097/JS9.0000000000002668.

DOI:10.1097/JS9.0000000000002668
PMID:40549442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12430928/
Abstract

Sepsis is a life-threatening multi-organ dysfunction caused by the dysregulated systemic inflammatory and immune responses in the host to an infection. Despite continuous advances in the treatment of sepsis, its high morbidity and mortality seriously challenge global public health. Symptomatic treatments are currently applied to sepsis patients, while precise treatments acting on the individualized etiological and pathogenic factors are scant. To address the issue, the present review aims to illustrate the pathogenic mechanisms of Gram-negative bacteria, the immune imbalance of co-existing continuous inflammation and immunosuppression, and the increased susceptibility resulting from the imbalanced gut microbiota. Moreover, we summarized the therapeutic strategies for sepsis and the development of precise treatment acting on sepsis patients' individualized subphenotypes and immune statuses. From the perspectives of etiological factors, pathogenesis, and precision treatment, we provide new insights into the future treatment of sepsis.

摘要

脓毒症是由宿主对感染的系统性炎症和免疫反应失调引起的危及生命的多器官功能障碍。尽管脓毒症治疗不断取得进展,但其高发病率和死亡率严重挑战全球公共卫生。目前脓毒症患者采用对症治疗,而针对个体化病因和致病因素的精准治疗却很少。为解决这一问题,本综述旨在阐述革兰氏阴性菌的致病机制、持续炎症和免疫抑制并存的免疫失衡以及肠道微生物群失衡导致的易感性增加。此外,我们总结了脓毒症的治疗策略以及针对脓毒症患者个体化亚表型和免疫状态的精准治疗进展。从病因、发病机制和精准治疗的角度,我们为脓毒症的未来治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/36a58c7d084d/js9-111-6260-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/4816547e4dd7/js9-111-6260-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/36a58c7d084d/js9-111-6260-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/4816547e4dd7/js9-111-6260-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/0f4d8c6ed6d1/js9-111-6260-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/cdacb877b02e/js9-111-6260-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/3e092c865afe/js9-111-6260-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdf/12430928/36a58c7d084d/js9-111-6260-g005.jpg

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本文引用的文献

1
The Mechanisms of Sepsis Induced Coagulation Dysfunction and Its Treatment.脓毒症诱导凝血功能障碍的机制及其治疗
J Inflamm Res. 2025 Feb 3;18:1479-1495. doi: 10.2147/JIR.S504184. eCollection 2025.
2
The efficacy and safety of thymosin α1 for sepsis (TESTS): multicentre, double blinded, randomised, placebo controlled, phase 3 trial.胸腺肽α1治疗脓毒症的疗效和安全性研究(TESTS):多中心、双盲、随机、安慰剂对照3期试验
BMJ. 2025 Jan 15;388:e082583. doi: 10.1136/bmj-2024-082583.
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Corticosteroids for Sepsis, Acute Respiratory Distress Syndrome, or Community-Acquired Pneumonia.
用于脓毒症、急性呼吸窘迫综合征或社区获得性肺炎的皮质类固醇。
JAMA. 2025 Feb 4;333(5):421-422. doi: 10.1001/jama.2024.24537.
4
Brain natriuretic peptide as a predictive marker of mortality in sepsis: an updated systematic review and meta-analysis.脑钠肽作为脓毒症死亡率的预测标志物:一项更新的系统评价和荟萃分析
BMC Anesthesiol. 2024 Aug 7;24(1):276. doi: 10.1186/s12871-024-02661-z.
5
Usefulness of myocardial damage biomarkers in predicting cardiogenic shock in patients undergoing heart valve surgery.心肌损伤生物标志物在预测心脏瓣膜手术患者心源性休克中的应用价值。
Kardiol Pol. 2024;82(4):423-426. doi: 10.33963/v.phj.99553. Epub 2024 Mar 17.
6
Multidrug-Resistant Sepsis: A Critical Healthcare Challenge.多重耐药性脓毒症:一项严峻的医疗保健挑战。
Antibiotics (Basel). 2024 Jan 4;13(1):46. doi: 10.3390/antibiotics13010046.
7
The pathophysiology of sepsis and precision-medicine-based immunotherapy.脓毒症的病理生理学与基于精准医学的免疫治疗。
Nat Immunol. 2024 Jan;25(1):19-28. doi: 10.1038/s41590-023-01660-5. Epub 2024 Jan 2.
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Curr Med Res Opin. 2024 Jan;40(1):11-13. doi: 10.1080/03007995.2023.2286102. Epub 2024 Jan 3.
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