Type I interferon in the pathogenesis of systemic lupus erythematosus. (December 2020)
- Record Type:
- Journal Article
- Title:
- Type I interferon in the pathogenesis of systemic lupus erythematosus. (December 2020)
- Main Title:
- Type I interferon in the pathogenesis of systemic lupus erythematosus
- Authors:
- Postal, Mariana
Vivaldo, Jessica F
Fernandez-Ruiz, Ruth
Paredes, Jacqueline L
Appenzeller, Simone
Niewold, Timothy B - Abstract:
- Highlights: Type I IFN is implicated in SLE pathogenesis by multiple lines of evidence, including genetics and induction of SLE by IFN treatment. Nucleic-acid sensing pathways influence the threshold of activation and triggering of type I IFN production. Abnormalities in extracellular processing of DNA can enhance type I IFN production. High type I IFN levels are associated with nephritis, mucocutaneous manifestations, and the presence of autoantibodies in SLE. Anifrolumab, a monoclonal antibody that blocks the type I IFN receptor, has shown therapeutic benefit in SLE. Abstract : Type I interferon (IFN) is a primary pathogenic factor in systemic lupus erythematosus (SLE). Gain-of-function genetic variants in the type I IFN pathway have been associated with risk of disease. Common polygenic as well as rare monogenic influences on type I IFN have been demonstrated, supporting a complex genetic basis for high IFN in many SLE patients. Both SLE-associated autoantibodies and high type I IFN can be observed in the pre-disease state. Patients with SLE and evidence of high type I IFN have more active disease and a greater propensity to nephritis and other severe manifestations. Despite the well-established association between type I IFN and SLE, the specific triggers of type I IFN production, the mechanisms by which IFNs help perpetuate the cycle of autoreactive cells and autoantibody production are not completely clear. This review provides an updated overview of type I IFN in SLEHighlights: Type I IFN is implicated in SLE pathogenesis by multiple lines of evidence, including genetics and induction of SLE by IFN treatment. Nucleic-acid sensing pathways influence the threshold of activation and triggering of type I IFN production. Abnormalities in extracellular processing of DNA can enhance type I IFN production. High type I IFN levels are associated with nephritis, mucocutaneous manifestations, and the presence of autoantibodies in SLE. Anifrolumab, a monoclonal antibody that blocks the type I IFN receptor, has shown therapeutic benefit in SLE. Abstract : Type I interferon (IFN) is a primary pathogenic factor in systemic lupus erythematosus (SLE). Gain-of-function genetic variants in the type I IFN pathway have been associated with risk of disease. Common polygenic as well as rare monogenic influences on type I IFN have been demonstrated, supporting a complex genetic basis for high IFN in many SLE patients. Both SLE-associated autoantibodies and high type I IFN can be observed in the pre-disease state. Patients with SLE and evidence of high type I IFN have more active disease and a greater propensity to nephritis and other severe manifestations. Despite the well-established association between type I IFN and SLE, the specific triggers of type I IFN production, the mechanisms by which IFNs help perpetuate the cycle of autoreactive cells and autoantibody production are not completely clear. This review provides an updated overview of type I IFN in SLE pathogenesis, clinical manifestations, and current therapeutic strategies targeting this pathway. … (more)
- Is Part Of:
- Current opinion in immunology. Volume 67(2020)
- Journal:
- Current opinion in immunology
- Issue:
- Volume 67(2020)
- Issue Display:
- Volume 67, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 67
- Issue:
- 2020
- Issue Sort Value:
- 2020-0067-2020-0000
- Page Start:
- 87
- Page End:
- 94
- Publication Date:
- 2020-12
- Subjects:
- Immunology -- Periodicals
Allergy -- Periodicals
Immunology -- Abstracts -- Periodicals
Allergy -- Abstracts -- Periodicals
616.079 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09527915 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.coi.2020.10.014 ↗
- Languages:
- English
- ISSNs:
- 0952-7915
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.775300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15369.xml