The complement system and toll-like receptors as integrated players in the pathophysiology of atherosclerosis. Issue 2 (August 2015)
- Record Type:
- Journal Article
- Title:
- The complement system and toll-like receptors as integrated players in the pathophysiology of atherosclerosis. Issue 2 (August 2015)
- Main Title:
- The complement system and toll-like receptors as integrated players in the pathophysiology of atherosclerosis
- Authors:
- Hovland, Anders
Jonasson, Lena
Garred, Peter
Yndestad, Arne
Aukrust, Pål
Lappegård, Knut T.
Espevik, Terje
Mollnes, Tom E. - Abstract:
- Abstract: Despite recent medical advances, atherosclerosis is a global burden accounting for numerous deaths and hospital admissions. Immune-mediated inflammation is a major component of the atherosclerotic process, but earlier research focus on adaptive immunity has gradually switched towards the role of innate immunity. The complement system and toll-like receptors (TLRs), and the crosstalk between them, may be of particular interest both with respect to pathogenesis and as therapeutic targets in atherosclerosis. Animal studies indicate that inhibition of C3a and C5a reduces atherosclerosis. In humans modified LDL-cholesterol activate complement and TLRs leading to downstream inflammation, and histopathological studies indicate that the innate immune system is present in atherosclerotic lesions. Moreover, clinical studies have demonstrated that both complement and TLRs are upregulated in atherosclerotic diseases, although interventional trials have this far been disappointing. However, based on recent research showing an intimate interplay between complement and TLRs we propose a model in which combined inhibition of both complement and TLRs may represent a potent anti-inflammatory therapeutic approach to reduce atherosclerosis. Highlights: Innate immunity is an important player in the inflammatory process underlying atherosclerosis. The complement system and the Toll-like receptor family are two main branches of innate immunity. Complement and Toll-like receptors areAbstract: Despite recent medical advances, atherosclerosis is a global burden accounting for numerous deaths and hospital admissions. Immune-mediated inflammation is a major component of the atherosclerotic process, but earlier research focus on adaptive immunity has gradually switched towards the role of innate immunity. The complement system and toll-like receptors (TLRs), and the crosstalk between them, may be of particular interest both with respect to pathogenesis and as therapeutic targets in atherosclerosis. Animal studies indicate that inhibition of C3a and C5a reduces atherosclerosis. In humans modified LDL-cholesterol activate complement and TLRs leading to downstream inflammation, and histopathological studies indicate that the innate immune system is present in atherosclerotic lesions. Moreover, clinical studies have demonstrated that both complement and TLRs are upregulated in atherosclerotic diseases, although interventional trials have this far been disappointing. However, based on recent research showing an intimate interplay between complement and TLRs we propose a model in which combined inhibition of both complement and TLRs may represent a potent anti-inflammatory therapeutic approach to reduce atherosclerosis. Highlights: Innate immunity is an important player in the inflammatory process underlying atherosclerosis. The complement system and the Toll-like receptor family are two main branches of innate immunity. Complement and Toll-like receptors are upregulated in atherosclerosis. The two systems cross-talk intensively and are possible targets for treatment of atherosclerosis. … (more)
- Is Part Of:
- Atherosclerosis. Volume 241:Issue 2(2015)
- Journal:
- Atherosclerosis
- Issue:
- Volume 241:Issue 2(2015)
- Issue Display:
- Volume 241, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 241
- Issue:
- 2
- Issue Sort Value:
- 2015-0241-0002-0000
- Page Start:
- 480
- Page End:
- 494
- Publication Date:
- 2015-08
- Subjects:
- The complement system -- Toll-like receptors -- Atherosclerosis -- Inflammation
Arteriosclerosis -- Periodicals
Electronic journals
616.136 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00219150 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/00219150 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.atherosclerosis.2015.05.038 ↗
- Languages:
- English
- ISSNs:
- 0021-9150
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1765.874000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21863.xml