DAMPs, PAMPs and alarmins: all we need to know about danger
Abstract
Multicellular animals detect pathogens via a set of receptors that recognize pathogen-associated molecular patterns (PAMPs). However, pathogens are not the only causative agents of tissue and cell damage: trauma is another one. Evidence is accumulating that trauma and its associated tissue damage are recognized at the cell level via receptor-mediated detection of intracellular proteins released by the dead cells. The term “alarmin” is proposed to categorize such endogenous molecules that signal tissue and cell damage. Intriguingly, effector cells of innate and adaptive immunity can secrete alarmins via nonclassical pathways and often do so when they are activated by PAMPs or other alarmins. Endogenous alarmins and exogenous PAMPs therefore convey a similar message and elicit similar responses; they can be considered subgroups of a larger set, the damage-associated molecular patterns (DAMPs).
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HMGB1 is a DNA structural protein that has been co-opted by the innate immune system to signal damage during sterile inflammatory conditions.
“HMGB1 is a DNA structural protein that has been co-opted by the innate immune system to signal damage during sterile inflammatory conditions (Bianchi, 2007).”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Bianchi, 2007
An acute mental or physical stressor that primarily activates systems under CNS control (HPA axis and ANS) will also induce an inflammatory response.
“an acute mental or physical stressor that primarily activates systems under CNS control, i.e., the neuroendocrine hypothalamus-pituitary-adrenal (HPA) axis and the autonomic nervous system (ANS), will also induce an inflammatory response (52, 525).”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [52]
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References 60 · Cited by 2,794
- Authors
- Bianchi, M. E.
- Affiliations
- Vita-Salute San Raffaele University (IT)
- Corresponding author
- Bianchi, Marco E
- ORCID
- Bianchi, Marco E
- Venue
- Journal of Leukocyte Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-10-10
- Volume
- 81
- Issue
- 1
- Pages
- 1-5
- ISSN
- 0741-5400 (ISSN-L)
- 1938-3673
- OpenAlex
- W2150594596
- Cited by
- 2,794
- References
- 60
- Citations by year
- 2026: 42 · 2025: 75 · 2024: 85 · 2023: 108 · 2022: 119 · 2021: 167 · 2020: 158 · 2019: 134 · 2018: 161 · 2017: 172 · 2016: 179 · 2015: 198 · 2014: 185 · 2013: 197 · 2012: 216
- FWCI
- 6.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Leukocyte Biology (publishedVersion)
- PubMed (publishedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- Funders
- Italian Association for Cancer Research
- International Cancer Research
- Ministry of University and Research
- Fondazione Cariplo and Fondazione Monte dei Paschi di Siena
- 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 › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Keywords
- damage-associated molecular patterns, pathogen-associated molecular patterns, alarmins, tissue damage, trauma (physical injury), innate immunity, adaptive immunity, intracellular protein release
- MeSH terms
- Animals, Heat-Shock Proteins, Receptors, Immunologic, Uric Acid, Signal Transduction, HMGB1 Protein, Calgranulin A, Toll-Like Receptors, Mice, Interleukin-1alpha
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