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               <mods:identifier type="citation">Cell Rep. 2022 Oct 11;41(2):111468</mods:identifier>
               <mods:identifier type="doi">10.1016/j.celrep.2022.111468</mods:identifier>
               <mods:identifier type="e-issn">2211-1247</mods:identifier>
               <mods:identifier type="journal">Cell reports</mods:identifier>
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               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/15256</mods:identifier>
               <mods:abstract>Atherosclerosis is a chronic inflammatory disease of the arteries that can lead to thrombosis, infarction, and stroke and is the leading cause of mortality worldwide. Immunization of pro-atherogenic mice with malondialdehyde-modified low-density lipoprotein (MDA-LDL) neo-antigen is athero-protective. However, the immune response to MDA-LDL and the mechanisms responsible for this athero-protection are not completely understood. Here, we find that immunization of mice with MDA-LDL elicits memory B cells, plasma cells, and switched anti-MDA-LDL antibodies as well as clonal expansion and affinity maturation, indicating that MDA-LDL triggers a bona fide germinal center antibody response. Further, Prdm1fl/flAicda-Cre+/kiLdlr-/- pro-atherogenic chimeras, which lack germinal center-derived plasma cells, show accelerated atherosclerosis. Finally, we show that MDA-LDL immunization is not athero-protective in mice lacking germinal-center-derived plasma cells. Our findings give further support to the development of MDA-LDL-based vaccines for the prevention or treatment of atherosclerosis.</mods:abstract>
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                  <mods:title>MDA-LDL vaccination induces athero-protective germinal-center-derived antibody responses.</mods:title>
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