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      DAMPs, PAMPs, and LAMPs in Immunity and Sterile Inflammation

      1 , 2 , 3 , 4 , 1 , 2 , 5
      Annual Review of Pathology: Mechanisms of Disease
      Annual Reviews

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          Abstract

          Recognizing the importance of leukocyte trafficking in inflammation led to some therapeutic breakthroughs. However, many inflammatory pathologies remain without specific therapy. This review discusses leukocytes in the context of sterile inflammation, a process caused by sterile (non-microbial) molecules, comprising damage-associated molecular patterns (DAMPs). DAMPs bind specific receptors to activate inflammation and start a highly optimized sequence of immune cell recruitment of neutrophils and monocytes to initiate effective tissue repair. When DAMPs are cleared, the recruited leukocytes change from a proinflammatory to a reparative program, a switch that is locally supervised by invariant natural killer T cells. In addition, neutrophils exit the inflammatory site and reverse transmigrate back to the bloodstream. Inflammation persists when the program switch or reverse transmigration fails, or when the coordinated leukocyte effort cannot clear the immunostimulatory molecules. The latter causes inappropriate leukocyte activation, a driver of many pathologies associated with poor lifestyle choices. We discuss lifestyle-associated inflammatory diseases and their corresponding immunostimulatory lifestyle-associated molecular patterns (LAMPs) and distinguish them from DAMPs.

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          Author and article information

          Journal
          Annual Review of Pathology: Mechanisms of Disease
          Annu. Rev. Pathol. Mech. Dis.
          Annual Reviews
          1553-4006
          1553-4014
          January 24 2020
          January 24 2020
          : 15
          : 1
          : 493-518
          Affiliations
          [1 ]Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta T2N 4N1, Canada;
          [2 ]Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada
          [3 ]Department of Visceral Surgery and Medicine, Department for BioMedical Research, University of Bern, CH-3008 Bern, Switzerland
          [4 ]Graduate School for Cellular and Biomedical Sciences, University of Bern, CH-3012 Bern, Switzerland
          [5 ]Department of Microbiology, Immunology & Infectious Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada
          Article
          10.1146/annurev-pathmechdis-012419-032847
          31675482
          68c67b97-b7c5-48e8-9a3c-7e8a2ac606be
          © 2020
          History

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