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Trends Cardiovasc Med. 2012 Feb;22(2):48-53. doi: 10.1016/j.tcm.2012.06.011. Epub 2012 Jul 28.

Protective role of natural IgM-producing B1a cells in atherosclerosis.

Author information

1
Vascular Biology and Atherosclerosis Laboratory, Baker IDI Heart and Diabetes Institute, Melbourne, VIC 3004, Australia.

Abstract

Atherosclerosis initiated by hyperlipidemia is modulated by immune cells in its development, progression, and rupture that results in thrombotic arterial occlusion leading to strokes and myocardial infarction. B cells initially thought to be atheroprotective provide opposing roles by their different subsets. Unlike B2 cells that are atherogenic, serosal B1a cells are atheroprotective by producing natural IgM antibodies that clear modified low-density lipoprotein and apoptotic and necrotic debris. In addition to natural IgM antibodies, B1a cells may act as regulatory B cells by producing the anti-inflammatory cytokine interleukin-10, which inhibits proinflammatory cytokines secreted by activated macrophages and T cells in atherosclerotic lesions. These findings suggest in vivo expansion of atheroprotective B1a cells as a potential therapeutic strategy to augment the benefits of lipid-lowering statin therapy.

PMID:
22841841
DOI:
10.1016/j.tcm.2012.06.011
[Indexed for MEDLINE]

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