Abstract | OBJECTIVES: BACKGROUND: METHODS:
Apolipoprotein E knockout mice were immunized with PC every second week over 4 months. At the end of the study, serum antibodies directed to either PC or oxLDL were measured. Splenic and peritoneal B cells were analyzed by flow cytometry. Aortic root atherosclerotic lesions were quantified by morphometry and phenotyped by immunohistochemistry. Immune and control sera were also tested for their effect on foam cell formation in macrophage culture in the presence of oxLDL. RESULTS: The PC-immunized mice showed 3-fold increase in titers of anti-PC and - oxLDL antibodies compared with control mice (p < 0.01). The PC-immunized mice also showed a significant increase in the number of splenic mature B cells. The extent of atherosclerotic aorta root lesions was reduced by >40% in the PC-immunized mice (p < 0.01). Immunohistochemistry showed reduced expression of major histocompatibility complex class II antigens (p < 0.05) and the presence of B-cell clusters in plaques of PC-immunized mice. Finally, PC-immune serum was able to reduce macrophage-derived foam cell formation in the presence of oxLDL in vitro. CONCLUSIONS:
Phosphorylcholine immunization drives a specific humoral immune response that reduces foam cell formation in vitro and is atheroprotective in vivo.
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Authors | Giuseppina Caligiuri, Jamila Khallou-Laschet, Marta Vandaele, Anh-Thu Gaston, Sandrine Delignat, Chantal Mandet, Heinz V Kohler, Srini V Kaveri, Antonino Nicoletti |
Journal | Journal of the American College of Cardiology
(J Am Coll Cardiol)
Vol. 50
Issue 6
Pg. 540-6
(Aug 07 2007)
ISSN: 1558-3597 [Electronic] United States |
PMID | 17678738
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies
- Immune Sera
- Lipoproteins, LDL
- oxidized low density lipoprotein
- Phosphorylcholine
- Hemocyanins
- keyhole-limpet hemocyanin
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Topics |
- Animals
- Antibodies
(blood, therapeutic use)
- Antibody Formation
(physiology)
- Atherosclerosis
(immunology, physiopathology, therapy)
- B-Lymphocytes
(physiology)
- Cells, Cultured
- Female
- Hemocyanins
(immunology)
- Immune Sera
(pharmacology)
- Immunization, Passive
(methods)
- Lipoproteins, LDL
(immunology, metabolism)
- Macrophages
(drug effects, metabolism)
- Mice
- Mice, Knockout
- Phosphorylcholine
(immunology)
- Streptococcus pneumoniae
(immunology)
- Vaccination
(methods)
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