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Physiological and Pathological Inflammation Induced by Antibodies and Pentraxins.
- Source :
-
Cells [Cells] 2021 May 12; Vol. 10 (5). Date of Electronic Publication: 2021 May 12. - Publication Year :
- 2021
-
Abstract
- Macrophages play a key role in induction of inflammatory responses. These inflammatory responses are mostly considered to be instigated by activation of pattern recognition receptors (PRRs) or cytokine receptors. However, recently it has become clear that also antibodies and pentraxins, which can both activate Fc receptors (FcRs), induce very powerful inflammatory responses by macrophages that can even be an order of magnitude greater than PRRs. While the physiological function of this antibody-dependent inflammation (ADI) is to counteract infections, undesired activation or over-activation of this mechanism will lead to pathology, as observed in a variety of disorders, including viral infections such as COVID-19, chronic inflammatory disorders such as Crohn's disease, and autoimmune diseases such as rheumatoid arthritis. In this review we discuss how physiological ADI provides host defense by inducing pathogen-specific immunity, and how erroneous activation of this mechanism leads to pathology. Moreover, we will provide an overview of the currently known signaling and metabolic pathways that underlie ADI, and how these can be targeted to counteract pathological inflammation.
- Subjects :
- Antibodies immunology
C-Reactive Protein immunology
Host-Pathogen Interactions immunology
Humans
Immunity, Innate
Inflammation metabolism
Inflammation microbiology
Macrophages immunology
Macrophages metabolism
Metabolic Networks and Pathways immunology
Receptors, Fc metabolism
Serum Amyloid P-Component immunology
Signal Transduction immunology
Antibodies metabolism
C-Reactive Protein metabolism
Inflammation immunology
Serum Amyloid P-Component metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 10
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 34065953
- Full Text :
- https://doi.org/10.3390/cells10051175