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Protective immunity against atherosclerosis carried by B cells of hypercholesterolemic mice
Giuseppina Caligiuri, … , Bruno Poirier, Göran K. Hansson
Giuseppina Caligiuri, … , Bruno Poirier, Göran K. Hansson
Published March 15, 2002
Citation Information: J Clin Invest. 2002;109(6):745-753. https://doi.org/10.1172/JCI7272.
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Article

Protective immunity against atherosclerosis carried by B cells of hypercholesterolemic mice

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Abstract

Atherosclerosis is characterized by vascular inflammation and associated with systemic and local immune responses to oxidized LDL (oxLDL) and other antigens. Since immunization with oxLDL reduces atherosclerosis, we hypothesized that the disease might be associated with development of protective immunity. Here we show that spleen-associated immune activity protects against atherosclerosis. Splenectomy dramatically aggravated atherosclerosis in hypercholesterolemic apoE knockout (apoE°) mice. Transfer of spleen cells from atherosclerotic apoE° mice significantly reduced disease development in young apoE° mice. To identify the protective subset, donor spleen cells were divided into B and T cells by immunomagnetic separation before transfer. Protection was conferred by B cells, which reduced disease in splenectomized apoE° mice to one-fourth of that in splenectomized apoE° controls. Protection could also be demonstrated in intact, nonsplenectomized mice and was associated with an increase in antibody titers to oxLDL. Fewer CD4+ T cells were found in lesions of protected mice, suggesting a role for T-B cell cooperation. These results demonstrate that B cell–associated protective immunity develops during atherosclerosis and reduces disease progression.

Authors

Giuseppina Caligiuri, Antonino Nicoletti, Bruno Poirier, Göran K. Hansson

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Figure 3

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Effect of splenectomy and cell transfer on antibody titers to MDA-LDL. E...
Effect of splenectomy and cell transfer on antibody titers to MDA-LDL. ELISA of IgM and IgG antibodies to MDA-LDL was performed in splenectomized (Sx), sham-operated, and untouched apoE° mice and in Sx mice that had received total spleen cells or isolated T or B cells from atherosclerotic, 20-week-old apoE° mice. Data show binding of IgM and IgG from diluted mouse sera to MDA-LDL–coated plates (mean absorbance). Insets: ELISA of IgM and IgG antibodies to MDA-LDL (continuous lines) and nLDL (dashed lines) in untouched apoE° mice (means ± SEM). Incubation on plates coated with native LDL resulted in absorbance levels <0.1 in all treatment groups (data not shown). n = 4 mice per group.

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