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DAMPs and NETs in Sepsis

Open access
Denning, Naomi-Liza, Aziz, Monowar, Gurien, Steven D., Wang, Ping·2019·Frontiers in Immunology

Abstract

Sepsis is a deadly inflammatory syndrome caused by an exaggerated immune response to infection. Much has been focused on host response to pathogens mediated through the interaction of pathogen-associated molecular patterns (PAMPs) and pattern recognition receptors (PRRs). PRRs are also activated by host nuclear, mitochondrial, and cytosolic proteins, known as damage-associated molecular patterns (DAMPs) that are released from cells during sepsis. Some well described members of the DAMP family are extracellular cold-inducible RNA-binding protein (eCIRP), high mobility group box 1 (HMGB1), histones, and adenosine triphosphate (ATP). DAMPs are released from the cell through inflammasome activation or passively following cell death. Similarly, neutrophil extracellular traps (NETs) are released from neutrophils during inflammation. NETs are webs of extracellular DNA decorated with histones, myeloperoxidase, and elastase. Although NETs contribute to pathogen clearance, excessive NET formation promotes inflammation and tissue damage in sepsis. Here, we review DAMPs and NETs and their crosstalk in sepsis with respect to their sources, activation, release, and function. A clear grasp of DAMPs, NETs and their interaction is crucial for the understanding of the pathophysiology of sepsis and for the development of novel sepsis therapeutics.

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Metadata

Authors
Denning, N.-L., Aziz, M., Gurien, S. D., & Wang, P.
Venue
Frontiers in Immunology
Published
2019-10-30
Volume
10
Pages
2536-2536
ISSN
1664-3224 (ISSN-L)
OpenAlex
W2982600436
Cited by
623
References
192
FWCI
17.38
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: DAMPs and NETs in Sepsis. https://app.cochat.ai/papers/10.3389/fimmu.2019.02536
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Denning, N.-L., Aziz, M., Gurien, S. D., & Wang, P. (2019). DAMPs and NETs in Sepsis. Frontiers in Immunology. https://doi.org/10.3389/fimmu.2019.02536

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