| Literature DB >> 10862788 |
P X Shaw1, S Hörkkö, M K Chang, L K Curtiss, W Palinski, G J Silverman, J L Witztum.
Abstract
The immune response to oxidized LDL (OxLDL) may play an important role in atherogenesis. Working with apoE-deficient mice, we isolated a panel of OxLDL-specific B-cell lines that secrete IgM Abs that specifically bind to oxidized phospholipids such as 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphorylcholine (POVPC). These Abs block uptake of OxLDL by macrophages, recognize similar oxidation-specific epitopes on apoptotic cells, and are deposited in atherosclerotic lesions. The Abs were found to be structurally and functionally identical to classic "natural" T15 anti-PC Abs that are of B-1 cell origin and are reported to provide optimal protection from virulent pneumococcal infection. These findings suggest that there has been natural selection for B-1 cells secreting oxidation-specific/T15 antibodies, both for their role in natural immune defense and for housekeeping roles against oxidation-dependent neodeterminants in health and disease.Entities:
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Year: 2000 PMID: 10862788 PMCID: PMC378505 DOI: 10.1172/JCI8472
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808