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The Sterile Inflammatory Response
Open accessAbstract
The acute inflammatory response is a double-edged sword. On the one hand, it plays a key role in initial host defense, particularly against many infections. On the other hand, its aim is imprecise, and as a consequence, when it is drawn into battle, it can cause collateral damage in tissues. In situations where the inciting stimulus is sterile, the cost-benefit ratio may be high; because of this, sterile inflammation underlies the pathogenesis of a number of diseases. Although there have been major advances in our understanding of how microbes trigger inflammation, much less has been learned about this process in sterile situations. This review focuses on a subset of the many sterile stimuli that can induce inflammation—specifically dead cells and a variety of irritant particles, including crystals, minerals, and protein aggregates. Although this subset of stimuli is structurally very diverse and might appear to be unrelated, there is accumulating evidence that the innate immune system may recognize them in similar ways and stimulate the sterile inflammatory response via common pathways. Here we review established and emerging data about these responses.
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The consequence of PRR-DAMP binding is sterile inflammation.
“The consequence of PRR-DAMP binding is sterile inflammation (Kono and Rock, 2008;Rock et al, 2010).”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Rock et al, 2010
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References 122 · Cited by 865
Research works printed but not linked: 6
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- Waller A, 1846, Philos. Mag. (3rd Series), 29, 397
- 7. Majno G, Joris I. 2004. Cells, Tissues and Diseases: Principles of General Pathology . Cambridge, MA: Oxford Univ. Press, 1040pp.
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Metadata
- Authors
- Rock, K. L., Latz, E., Ontiveros, F., & Kono, H.
- Affiliations
- University of Massachusetts Chan Medical School (US)
- Venue
- Annual Review of Immunology
- Publisher
- Annual Reviews
- Published
- 2010-03-01
- Volume
- 28
- Issue
- 1
- Pages
- 321-342
- ISSN
- 0732-0582 (ISSN-L)
- 1545-3278
- PMC
- PMC4315152
- OpenAlex
- W2130989367
- Cited by
- 865
- References
- 122
- Citations by year
- 2026: 28 · 2025: 41 · 2024: 49 · 2023: 52 · 2022: 43 · 2021: 40 · 2020: 50 · 2019: 51 · 2018: 55 · 2017: 65 · 2016: 51 · 2015: 66 · 2014: 65 · 2013: 75 · 2012: 62
- FWCI
- 5.35
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Institutional Repositories DataBase (IRDB) (submittedVersion)
- Funders
- American Asthma Foundation
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01AI078287)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 32520, P30DK032520)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- sterile inflammation, innate immunity, dead cells, crystals, minerals, protein aggregates, host defense, tissue damage, inflammatory disease pathogenesis
- MeSH terms
- Animals, Humans, Immunity, Innate, Inflammation, Interleukin-1, Signal Transduction, Cell Death
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