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急性呼吸窘迫综合征细胞因子研究进展:综述

Progress in cytokine research for ARDS: A comprehensive review.

作者信息

Zhou Kaihuan, Lu Junyu

机构信息

Intensive Care Unit, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530007, China.

Intensive Care Unit, The Second Affiliated Hospital of Guangxi Medical University, No. 166 Daxuedong Road, Nanning, Guangxi 530007, China.

出版信息

Open Med (Wars). 2024 Oct 28;19(1):20241076. doi: 10.1515/med-2024-1076. eCollection 2024.

DOI:10.1515/med-2024-1076
PMID:39479463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11524396/
Abstract

INTRODUCTION

Acute respiratory distress syndrome (ARDS) is a critical form of acute respiratory failure characterized by diffuse alveolar damage, refractory hypoxemia, and non-cardiogenic pulmonary edema, resulting in high mortality. Dysregulated inflammation, driven by cytokines, is central to ARDS pathogenesis, progression, and prognosis.

OBJECTIVE

This review synthesizes current knowledge on the role of cytokines in ARDS and evaluates their potential as therapeutic targets, offering new insights for clinical management.

METHODS

A comprehensive analysis of recent studies was conducted to explore the roles of pro-inflammatory cytokines (e.g., IL-1β, IL-6, IL-8) and anti-inflammatory cytokines (e.g., IL-10, IL-22) in ARDS pathogenesis and to assess current and emerging therapies targeting these cytokines.

RESULTS

Pro-inflammatory cytokines are crucial in initiating inflammatory responses and lung injury in early ARDS, while anti-inflammatory cytokines help regulate and resolve inflammation. Targeted therapies, such as IL-1 and IL-6 inhibitors, show potential in managing ARDS, particularly in COVID-19, but their clinical efficacy is still debated. Combination therapy strategies may enhance outcomes, but further large-scale, multicenter randomized controlled trials are required to establish their safety and efficacy.

CONCLUSION

Understanding cytokine regulation in ARDS could lead to innovative therapeutic approaches. Future research should focus on cytokine roles across ARDS subtypes and stages and develop biomarker-driven, individualized treatments.

摘要

引言

急性呼吸窘迫综合征(ARDS)是急性呼吸衰竭的一种严重形式,其特征为弥漫性肺泡损伤、难治性低氧血症和非心源性肺水肿,导致高死亡率。由细胞因子驱动的炎症失调是ARDS发病机制、进展和预后的核心。

目的

本综述综合了关于细胞因子在ARDS中作用的现有知识,并评估它们作为治疗靶点的潜力,为临床管理提供新见解。

方法

对近期研究进行全面分析,以探讨促炎细胞因子(如IL-1β、IL-6、IL-8)和抗炎细胞因子(如IL-10、IL-22)在ARDS发病机制中的作用,并评估针对这些细胞因子的现有和新兴疗法。

结果

促炎细胞因子在早期ARDS引发炎症反应和肺损伤中起关键作用,而抗炎细胞因子有助于调节和消退炎症。靶向治疗,如IL-1和IL-6抑制剂,在管理ARDS方面显示出潜力,尤其是在COVID-19中,但它们的临床疗效仍存在争议。联合治疗策略可能会改善治疗结果,但需要进一步的大规模、多中心随机对照试验来确定其安全性和有效性。

结论

了解ARDS中的细胞因子调节可能会带来创新的治疗方法。未来的研究应关注细胞因子在ARDS各亚型和阶段中的作用,并开发基于生物标志物的个体化治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d03/11524396/6267f8341f2b/j_med-2024-1076-fig002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d03/11524396/cc200dfa4940/j_med-2024-1076-fig001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d03/11524396/6267f8341f2b/j_med-2024-1076-fig002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d03/11524396/cc200dfa4940/j_med-2024-1076-fig001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d03/11524396/6267f8341f2b/j_med-2024-1076-fig002.jpg

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本文引用的文献

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2
Advances in Biomarkers for Diagnosis and Treatment of ARDS.急性呼吸窘迫综合征诊断与治疗生物标志物的进展
Diagnostics (Basel). 2023 Oct 24;13(21):3296. doi: 10.3390/diagnostics13213296.
3
A New Global Definition of Acute Respiratory Distress Syndrome.急性呼吸窘迫综合征的新全球定义。
接受免疫检查点抑制剂治疗的肺癌患者发生检查点抑制剂肺炎的危险因素:一项系统评价和荟萃分析
Front Immunol. 2025 May 21;16:1607170. doi: 10.3389/fimmu.2025.1607170. eCollection 2025.
4
Morphopathology of the lesions induced by SARS-CoV-2 infection in the lungs.严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)感染所致肺部病变的形态病理学
Rom J Morphol Embryol. 2024 Oct-Dec;65(4):637-645. doi: 10.47162/RJME.65.4.10.
5
Acute respiratory distress syndrome (ARDS): from mechanistic insights to therapeutic strategies.急性呼吸窘迫综合征(ARDS):从机制洞察到治疗策略
MedComm (2020). 2025 Jan 26;6(2):e70074. doi: 10.1002/mco2.70074. eCollection 2025 Feb.
Am J Respir Crit Care Med. 2024 Jan 1;209(1):37-47. doi: 10.1164/rccm.202303-0558WS.
4
Targeted removal of macrophage-secreted interleukin-1 receptor antagonist protects against lethal Candida albicans sepsis.靶向清除巨噬细胞分泌的白细胞介素-1 受体拮抗剂可预防致死性白色念珠菌败血症。
Immunity. 2023 Aug 8;56(8):1743-1760.e9. doi: 10.1016/j.immuni.2023.06.023. Epub 2023 Jul 20.
5
Shared inflammatory pathways of rheumatoid arthritis and atherosclerotic cardiovascular disease.类风湿关节炎和动脉粥样硬化性心血管疾病的共同炎症通路。
Nat Rev Rheumatol. 2023 Jul;19(7):417-428. doi: 10.1038/s41584-023-00969-7. Epub 2023 May 25.
6
Randomized phase II clinical trial of ruxolitinib plus simvastatin in COVID19 clinical outcome and cytokine evolution.随机对照 2 期临床试验:芦可替尼联合辛伐他汀治疗 COVID19 的临床结局和细胞因子变化。
Front Immunol. 2023 Apr 18;14:1156603. doi: 10.3389/fimmu.2023.1156603. eCollection 2023.
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The role of immunometabolism in macrophage polarization and its impact on acute lung injury/acute respiratory distress syndrome.免疫代谢在巨噬细胞极化中的作用及其对急性肺损伤/急性呼吸窘迫综合征的影响。
Front Immunol. 2023 Mar 20;14:1117548. doi: 10.3389/fimmu.2023.1117548. eCollection 2023.
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An important call: Suggestion of using IL-10 as therapeutic agent for COVID-19 with ARDS and other complications.一个重要的呼吁:建议使用 IL-10 作为 COVID-19 伴有 ARDS 和其他并发症的治疗药物。
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9
Molecular Mechanisms of Neutrophil Extracellular Trap (NETs) Degradation.中性粒细胞胞外诱捕网(NETs)降解的分子机制。
Int J Mol Sci. 2023 Mar 3;24(5):4896. doi: 10.3390/ijms24054896.
10
Current Knowledge of Th22 Cell and IL-22 Functions in Infectious Diseases.Th22细胞与白细胞介素-22在传染病中的功能的当前认知
Pathogens. 2023 Jan 23;12(2):176. doi: 10.3390/pathogens12020176.