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Cytosolic nucleic acid sensing as driver of critical illness: mechanisms and advances in therapy.

作者信息

Chen Zhaorong, Behrendt Rayk, Wild Lennart, Schlee Martin, Bode Christian

机构信息

Department of Anesthesiology and Intensive Care Medicine, University Hospital Bonn, 53127, Bonn, Germany.

Institute of Clinical Chemistry and Clinical Pharmacology, University Hospital Bonn, 53127, Bonn, Germany.

出版信息

Signal Transduct Target Ther. 2025 Mar 19;10(1):90. doi: 10.1038/s41392-025-02174-2.


DOI:10.1038/s41392-025-02174-2
PMID:40102400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11920230/
Abstract

Nucleic acids from both self- and non-self-sources act as vital danger signals that trigger immune responses. Critical illnesses such as acute respiratory distress syndrome, sepsis, trauma and ischemia lead to the aberrant cytosolic accumulation and massive release of nucleic acids that are detected by antiviral innate immune receptors in the endosome or cytosol. Activation of receptors for deoxyribonucleic acids and ribonucleic acids triggers inflammation, a major contributor to morbidity and mortality in critically ill patients. In the past decade, there has been growing recognition of the therapeutic potential of targeting nucleic acid sensing in critical care. This review summarizes current knowledge of nucleic acid sensing in acute respiratory distress syndrome, sepsis, trauma and ischemia. Given the extensive research on nucleic acid sensing in common pathological conditions like cancer, autoimmune disorders, metabolic disorders and aging, we provide a comprehensive summary of nucleic acid sensing beyond critical illness to offer insights that may inform its role in critical conditions. Additionally, we discuss potential therapeutic strategies that specifically target nucleic acid sensing. By examining nucleic acid sources, sensor activation and function, as well as the impact of regulating these pathways across various acute diseases, we highlight the driving role of nucleic acid sensing in critical illness.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/22e9b6fedff9/41392_2025_2174_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/64b0dff207cd/41392_2025_2174_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/d13b431c4c74/41392_2025_2174_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/35fb3d199a11/41392_2025_2174_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/2bb0369f6f7b/41392_2025_2174_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/53a2bae073e7/41392_2025_2174_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/ef593e4a0f88/41392_2025_2174_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/22e9b6fedff9/41392_2025_2174_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/64b0dff207cd/41392_2025_2174_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/d13b431c4c74/41392_2025_2174_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/35fb3d199a11/41392_2025_2174_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/2bb0369f6f7b/41392_2025_2174_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/53a2bae073e7/41392_2025_2174_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/ef593e4a0f88/41392_2025_2174_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cd4/11920230/22e9b6fedff9/41392_2025_2174_Fig7_HTML.jpg

相似文献

[1]
Cytosolic nucleic acid sensing as driver of critical illness: mechanisms and advances in therapy.

Signal Transduct Target Ther. 2025-3-19

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[5]
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[8]
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[9]
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[10]
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引用本文的文献

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A feedback loop between DNA damage, genomic instability, and cytoplasmic DNA sensing contributes to cytokine production in COVID-19.

Arch Virol. 2025-8-11

本文引用的文献

[1]
HbA1c and leukocyte mtDNA levels as major factors associated with post-COVID-19 syndrome in type 2 diabetes patients.

Sci Rep. 2024-10-26

[2]
MDA5 Is a Major Determinant of Developing Symptoms in Critically Ill COVID-19 Patients.

Clin Rev Allergy Immunol. 2024-12

[3]
Taking AIM at Influenza: The Role of the AIM2 Inflammasome.

Viruses. 2024-9-27

[4]
MPO-DNA Complexes and cf-DNA in Patients with Sepsis and Their Clinical Value.

Biomedicines. 2024-9-26

[5]
MicroRNAs are enriched at COVID-19 genomic risk regions, and their blood levels correlate with the COVID-19 prognosis of cancer patients infected by SARS-CoV-2.

Mol Cancer. 2024-10-21

[6]
Decoding the multiple functions of ZBP1 in the mechanism of sepsis-induced acute lung injury.

Commun Biol. 2024-10-21

[7]
Damage-associated molecular patterns in bacteraemic infection, including a comparative analysis with bacterial DNA, a pathogen-associated molecular pattern.

Sci Rep. 2024-10-8

[8]
Extracellular vesicles in sepsis plasma mediate neuronal inflammation in the brain through miRNAs and innate immune signaling.

J Neuroinflammation. 2024-10-7

[9]
Elevated serum mtDNA in COVID-19 patients is linked to SARS-CoV-2 envelope protein targeting mitochondrial VDAC1, inducing apoptosis and mtDNA release.

Apoptosis. 2024-12

[10]
A promising application of kidney-specific cell-free DNA methylation markers in real-time monitoring sepsis-induced acute kidney injury.

Epigenetics. 2024-12

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