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Role of genetic alterations in the NLRP3 and CARD8 genes in health and disease
Örebro University, School of Health and Medical Sciences, Örebro University, Sweden.ORCID iD: 0000-0002-4589-6440
Örebro University, School of Health and Medical Sciences, Örebro University, Sweden.ORCID iD: 0000-0002-0278-4510
Örebro University, School of Health and Medical Sciences, Örebro University, Sweden.ORCID iD: 0000-0002-9826-0462
2015 (English)In: Mediators of Inflammation, ISSN 0962-9351, E-ISSN 1466-1861, article id 846782Article, review/survey (Refereed) Published
Abstract [en]

The complexity of a common inflammatory disease is influenced by multiple genetic and environmental factors contributing to the susceptibility of disease. Studies have reported that these exogenous and endogenous components may perturb the balance of innate immune response by activating the NLRP3 inflammasome. The multimeric NLRP3 complex results in the caspase-1 activation and the release of potent inflammatory cytokines, like IL-1β. Several studies have been performed on the association of the genetic alterations in genes encoding NLRP3 and CARD8 with the complex diseases with inflammatory background, like inflammatory bowel disease, cardiovascular diseases, rheumatoid arthritis, and type 1 diabetes. The aim of the present review is therefore to summarize the literature regarding genetic alterations in these genes and their association with health and disease.

Place, publisher, year, edition, pages
New York: Hindawi Publishing Corporation, 2015. article id 846782
Keywords [en]
NLRP3, inflammasome, polymorphism, CARD8
National Category
Immunology in the medical area
Research subject
Biomedicine
Identifiers
URN: urn:nbn:se:oru:diva-42795DOI: 10.1155/2015/846782ISI: 000350655400001Scopus ID: 2-s2.0-84924227184OAI: oai:DiVA.org:oru-42795DiVA, id: diva2:789480
Note

Funding Agencies:

Magnus Bergvalls Foundation

Sigurd and Elsa Goljes Minne (Lindhes Advokatbyrå AB)

Stiftelsen Gamla Tjänarinnor

Available from: 2015-02-19 Created: 2015-02-19 Last updated: 2023-05-23Bibliographically approved

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Paramel, GeenaSirsjö, AllanFransén, Karin

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