Key result
Distinct B cell subsets exert opposing atheroprotective and proatherogenic effects in ASCVD.
This review highlights the complex, context-dependent roles of different B cell subsets in atherosclerosis, suggesting potential targets for future immunomodulatory therapies.
Atherosclerotic cardiovascular disease (ASCVD) is increasingly recognized not just as a lipid-driven disease, but as a complex interplay between vascular cells and the immune system. Accumulating evidence highlights a central, yet heterogeneous role for B cells in atherogenesis, with distinct subsets displaying opposing roles. In this review, we provide an in-depth overview of the contributions of B cell subsets to ASCVD, including emerging insights into the roles and pathways of atheroprotective innate B cells producing IgM against oxidation-specific epitopes (IgMOSE) and newly appreciated age-associated B cells (ABCs), a distinct subset that accumulates with aging and potentially exacerbates atherosclerosis. By integrating insights from preclinical models and human studies, we describe the mechanisms through which B cell subsets influence ASCVD, including antigen presentation and immune checkpoint-mediated communication, secretion of cytokines and chemokines, and we highlight that humoral immunity in atherosclerosis reflects a context-dependent interplay between antibody effector properties and antigenic targets rather than antibody class alone. Finally, we explore how the advances in our understanding of B cells may guide the development of more targeted immunomodulatory therapies that enhance atheroprotective B cell functions while limiting atherogenic responses.
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Lems et al. (2026) conducted a review in Atherosclerotic cardiovascular disease (ASCVD). B cell subsets was evaluated. B cell subsets play a heterogeneous role in atherosclerotic cardiovascular disease, with distinct subsets like atheroprotective innate B cells and age-associated B cells displaying opposing effects.
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