Suppr超能文献

脓毒症和脓毒性休克的治疗进展:调节促炎和抗炎机制

Treatment Advances in Sepsis and Septic Shock: Modulating Pro- and Anti-Inflammatory Mechanisms.

作者信息

Marques Adriana, Torre Carla, Pinto Rui, Sepodes Bruno, Rocha João

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-003 Lisbon, Portugal.

Joaquim Chaves Saúde, Joaquim Chaves Laboratório de Análises Clínicas, Miraflores, 1495-069 Algés, Portugal.

出版信息

J Clin Med. 2023 Apr 15;12(8):2892. doi: 10.3390/jcm12082892.

Abstract

Sepsis is currently defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection, and it affects over 25 million people every year. Even more severe, septic shock is a subset of sepsis defined by persistent hypotension, and hospital mortality rates are higher than 40%. Although early sepsis mortality has greatly improved in the past few years, sepsis patients who survive the hyperinflammation and subsequent organ damage often die from long-term complications, such as secondary infection, and despite decades of clinical trials targeting this stage of the disease, currently, no sepsis-specific therapies exist. As new pathophysiological mechanisms have been uncovered, immunostimulatory therapy has emerged as a promising path forward. Highly investigated treatment strategies include cytokines and growth factors, immune checkpoint inhibitors, and even cellular therapies. There is much to be learned from related illnesses, and immunotherapy trials in oncology, as well as the recent COVID-19 pandemic, have greatly informed sepsis research. Although the journey ahead is a long one, the stratification of patients according to their immune status and the employment of combination therapies represent a hopeful way forward.

摘要

脓毒症目前被定义为宿主对感染的反应失调所导致的危及生命的器官功能障碍,每年影响超过2500万人。更为严重的是,感染性休克是脓毒症的一个子集,其定义为持续性低血压,医院死亡率高于40%。尽管在过去几年中,早期脓毒症死亡率有了很大改善,但在度过过度炎症反应及随后的器官损伤后存活下来的脓毒症患者,往往死于长期并发症,如继发感染,并且尽管针对该疾病这一阶段进行了数十年的临床试验,但目前尚无脓毒症特异性疗法。随着新的病理生理机制被发现,免疫刺激疗法已成为一条有前景的前进道路。深入研究的治疗策略包括细胞因子和生长因子、免疫检查点抑制剂,甚至细胞疗法。从相关疾病以及肿瘤学免疫治疗试验和最近的新冠疫情中,我们可以学到很多东西。尽管前方的道路漫长,但根据患者的免疫状态进行分层以及采用联合疗法是一条充满希望的前进道路。

相似文献

2
Sepsis Care Pathway 2019.
Qatar Med J. 2019 Nov 7;2019(2):4. doi: 10.5339/qmj.2019.qccc.4. eCollection 2019.
3
The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).
JAMA. 2016 Feb 23;315(8):801-10. doi: 10.1001/jama.2016.0287.
4
International Consensus Criteria for Pediatric Sepsis and Septic Shock.
JAMA. 2024 Feb 27;331(8):665-674. doi: 10.1001/jama.2024.0179.
6
Immune Deregulation in Sepsis and Septic Shock: Reversing Immune Paralysis by Targeting PD-1/PD-L1 Pathway.
Front Immunol. 2021 Feb 17;11:624279. doi: 10.3389/fimmu.2020.624279. eCollection 2020.
7
Advances in the Study of Immunosuppressive Mechanisms in Sepsis.
J Inflamm Res. 2023 Sep 8;16:3967-3981. doi: 10.2147/JIR.S426007. eCollection 2023.
8
Immunotherapy: A promising approach to reverse sepsis-induced immunosuppression.
Pharmacol Res. 2016 Sep;111:688-702. doi: 10.1016/j.phrs.2016.07.019. Epub 2016 Jul 25.
10
Sepsis and septic shock: pathophysiological and cardiovascular background as basis for therapy.
Acta Clin Belg. 2010 Sep-Oct;65(5):323-9. doi: 10.1179/acb.2010.070.

引用本文的文献

1
Evaluation of Testican-1 as a Sepsis Biomarker in Pyometra Cats.
Vet Med Sci. 2025 Sep;11(5):e70514. doi: 10.1002/vms3.70514.
2
Clinical and mechanistic relevance of high-dimensionality analysis of the paediatric sepsis immunome.
Front Immunol. 2025 May 13;16:1569096. doi: 10.3389/fimmu.2025.1569096. eCollection 2025.
3
Expression of Serum LMAN2 and Sestrin2 in Septic Shock Patients and Exploration of Their Prognostic Value.
J Inflamm Res. 2025 Mar 13;18:3713-3724. doi: 10.2147/JIR.S501719. eCollection 2025.
7
Sialyl Lewis Glycomimetics as E- and P-Selectin Antagonists Targeting Hyperinflammation.
ACS Med Chem Lett. 2024 Nov 9;16(1):64-71. doi: 10.1021/acsmedchemlett.4c00452. eCollection 2025 Jan 9.
9
Immune regulation and organ damage link adiponectin to sepsis.
Front Immunol. 2024 Nov 27;15:1444884. doi: 10.3389/fimmu.2024.1444884. eCollection 2024.
10
The Modulation of Septic Shock: A Proteomic Approach.
Int J Mol Sci. 2024 Oct 3;25(19):10641. doi: 10.3390/ijms251910641.

本文引用的文献

1
Embracing complexity in sepsis.
Crit Care. 2023 Mar 11;27(1):102. doi: 10.1186/s13054-023-04374-0.
3
Using heparan sulfate octadecasaccharide (18-mer) as a multi-target agent to protect against sepsis.
Proc Natl Acad Sci U S A. 2023 Jan 24;120(4):e2209528120. doi: 10.1073/pnas.2209528120. Epub 2023 Jan 17.
6
The End of "One Size Fits All" Sepsis Therapies: Toward an Individualized Approach.
Biomedicines. 2022 Sep 12;10(9):2260. doi: 10.3390/biomedicines10092260.
7
A guide to immunotherapy for COVID-19.
Nat Med. 2022 Jan;28(1):39-50. doi: 10.1038/s41591-021-01643-9. Epub 2022 Jan 21.
8
Signaling pathways and intervention therapies in sepsis.
Signal Transduct Target Ther. 2021 Nov 25;6(1):407. doi: 10.1038/s41392-021-00816-9.
9
The immunology of sepsis.
Immunity. 2021 Nov 9;54(11):2450-2464. doi: 10.1016/j.immuni.2021.10.012.
10
Long Non-Coding RNAs as Biomarkers and Therapeutic Targets in Sepsis.
Front Immunol. 2021 Sep 22;12:722004. doi: 10.3389/fimmu.2021.722004. eCollection 2021.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验