Abstract
While interleukin (IL)-1β plays an important role in combating the invading pathogen as part of the innate immune response, its dysregulation is responsible for a number of autoinflammatory disorders. Large IL-1β activating platforms, known as inflammasomes, can assemble in response to the detection of endogenous host and pathogen-associated danger molecules. Formation of these protein complexes results in the autocatalysis and activation of caspase-1, which processes precursor IL-1β into its secreted biologically active form. Inflammasome and IL-1β activity is required to efficiently control viral, bacterial and fungal pathogen infections. Conversely, excess IL-1β activity contributes to human disease, and its inhibition has proved therapeutically beneficial in the treatment of a spectrum of serious, yet relatively rare, heritable inflammasomopathies. Recently, inflammasome function has been implicated in more common human conditions, such as gout, type II diabetes and cancer. This raises the possibility that anti-IL-1 therapeutics may have broader applications than anticipated previously, and may be utilized across diverse disease states that are linked insidiously through unwanted or heightened inflammasome activity.
© 2011 The Authors. Clinical and Experimental Immunology © 2011 British Society for Immunology.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Animals
-
Anti-Inflammatory Agents / pharmacology
-
Bacterial Infections / immunology
-
Bacterial Infections / microbiology
-
Carrier Proteins / genetics
-
Carrier Proteins / immunology*
-
Carrier Proteins / metabolism
-
Caspase 1 / genetics
-
Caspase 1 / immunology*
-
Caspase 1 / metabolism
-
Diabetes Mellitus, Type 2 / drug therapy
-
Diabetes Mellitus, Type 2 / immunology
-
Diabetes Mellitus, Type 2 / pathology
-
Enzyme Activation
-
Enzyme Precursors / genetics
-
Enzyme Precursors / immunology
-
Enzyme Precursors / metabolism
-
Gene Expression Regulation
-
Gout / drug therapy
-
Gout / immunology
-
Gout / pathology
-
Hereditary Autoinflammatory Diseases / drug therapy
-
Hereditary Autoinflammatory Diseases / immunology*
-
Hereditary Autoinflammatory Diseases / pathology
-
Humans
-
Immunity, Innate*
-
Inflammasomes / genetics
-
Inflammasomes / immunology*
-
Inflammasomes / metabolism
-
Inflammation / drug therapy
-
Inflammation / immunology*
-
Interleukin-1beta / genetics
-
Interleukin-1beta / immunology*
-
Interleukin-1beta / metabolism
-
Mice
-
Mice, Transgenic
-
Molecular Targeted Therapy / methods
-
Mycoses / immunology
-
Mycoses / microbiology
-
NLR Family, Pyrin Domain-Containing 3 Protein
-
Neoplasms / drug therapy
-
Neoplasms / immunology
-
Neoplasms / pathology
-
Signal Transduction / immunology*
-
Virus Diseases / immunology
-
Virus Diseases / virology
Substances
-
Anti-Inflammatory Agents
-
Carrier Proteins
-
Enzyme Precursors
-
Inflammasomes
-
Interleukin-1beta
-
NLR Family, Pyrin Domain-Containing 3 Protein
-
NLRP3 protein, human
-
Caspase 1