Abstract
CANTOS (Canakinumab Antiinflammatory Thrombosis Outcome Study) confirmed interleukin (IL)–1β as an appealing therapeutic target for human atherosclerosis and related complications. However, there are serious gaps in our understanding of IL-1 production in atherosclerosis. Herein the authors show that complex plaques, or plaques derived from patients with suboptimally controlled hyperlipidemia, or on no or low-intensity statin therapy, demonstrated higher recruitable IL-1β production. Generation of mature IL-1β was matched by IL-1α release, and both were attenuated by inhibition of NLR family pyrin domain containing 3 or caspase. These findings support the inflammasome as the main pathway for IL-1α/β generation in atherosclerosis and high-intensity lipid-lowering therapies as primary and additional anti-IL-1-directed therapies as secondary interventions in high-risk patients.
Original language | English (US) |
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Pages (from-to) | 304-317 |
Number of pages | 14 |
Journal | JACC: Basic to Translational Science |
Volume | 4 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2019 |
Keywords
- atherosclerosis
- hypercholesterolemia
- inflammasome
- inflammation
- interleukin-1
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine