Interleukin-18 Inhibition Aggravates Atherosclerosis in Jak2 Clonal Hematopoiesis
Abstract
Clonal hematopoiesis (CH) driven by JAK2V617F is known to accelerate atherosclerosis through inflammasome activation and release of interleukin (IL)-1β and -18; yet, the specific contribution of IL-18 has remained unclear. In this study, we demonstrate that antibody inhibition of IL-18 in JAK2V617F CH mice increases plaque collagen but paradoxically promotes both early lesion growth and advanced necrotic core formation. Mechanistically, IL-18 blockade reverses absent in melanoma 2 inflammasome activation but shifts cell death toward apoptosis, and together with impaired efferocytosis, results in greater necrosis. These events are coordinated by reduced interferon gamma signaling, which enhances collagen deposition while decreasing expression of efferocytotic genes. Our findings challenge the prevailing notion that IL-18 inhibition stabilizes atherosclerotic plaques and provide new mechanistic insight into the interplay among inflammasome biology, adaptive immunity, and plaque stability.
Fields of Study & Subjects
Inflammasome and immune disorders
Myeloproliferative Neoplasms: Diagnosis and Treatment
Cytokine Signaling Pathways and Interactions
Publication details
- Journal / source
- JACC Basic to Translational Science
- Publisher
- Elsevier BV
- Volume
- 11
- Issue
- 3
- Pages
- 101463–101463
- Publication date
- 25 February 2026
- Language
- EN