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Paludan, S. R., Pradeu, T., Masters, S. L., & Mogensen, T. H. (2021). Constitutive immune mechanisms: Mediators of host defence and immune regulation. Nature Reviews. Immunology, 21(3), 137–150. 
Added by: Dr. Enrique Feoli (05/05/2022, 20:23)   Last edited by: Dr. Enrique Feoli (05/05/2022, 20:23)
Resource type: Journal Article
DOI: 10.1038/s41577-020-0391-5
ID no. (ISBN etc.): 1474-1733
BibTeX citation key: Paludan2021
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Categories: BioAcyl Corp
Subcategories: Constitutive innate immunity
Creators: Masters, Mogensen, Paludan, Pradeu
Collection: Nature Reviews. Immunology
Views: 2/259
Abstract
The immune system enables organisms to combat infections and to eliminate endogenous challenges. Immune responses can be evoked through diverse inducible pathways. However, various constitutive mechanisms are also required for immunocompetence. The inducible responses of pattern recognition receptors of the innate immune system and antigen-specific receptors of the adaptive immune system are highly effective, but they also have the potential to cause extensive immunopathology and tissue damage, as seen in many infectious and autoinflammatory diseases. By contrast, constitutive innate immune mechanisms, including restriction factors, basal autophagy and proteasomal degradation, tend to limit immune responses, with loss-of-function mutations in these pathways leading to inflammation. Although they function through a broad and heterogeneous set of mechanisms, the constitutive immune responses all function as early barriers to infection and aim to minimize any disruption of homeostasis. Supported by recent human and mouse data, in this Review we compare and contrast the inducible and constitutive mechanisms of immunosurveillance., Constitutive innate immune mechanisms, such as restriction factors, RNA interference, antimicrobial peptides, basal autophagy and proteasomal degradation, exert early host defence activities that also aim to minimize tissue damage and homeostatic disruption by limiting the activation of inducible innate immunity.
  
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