首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Immunization of low density lipoprotein (LDL) receptor-deficient rabbits with homologous malondialdehyde-modified LDL reduces atherogenesis.
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Immunization of low density lipoprotein (LDL) receptor-deficient rabbits with homologous malondialdehyde-modified LDL reduces atherogenesis.

机译:对低密度脂蛋白(LDL)受体缺陷的兔进行同源丙二醛修饰的LDL免疫可以减少动脉粥样硬化的发生。

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摘要

Atherosclerotic lesions contain oxidized LDL (OxLDL), immunoglobulins, and immune-competent cells. Low levels of circulating autoantibodies against malondialdehyde (MDA)-modified lysine, an epitope of OxLDL, occur in several species, and immune complexes between such autoantibodies and OxLDL are present in lesions. To study the potential role of autoantibodies against OxLDL in the atherogenic process, we prospectively hyperimmunized LDL receptor-deficient rabbits with homologous MDA-LDL and determined the effects of this intervention on the development of atherosclerosis. Immunization with MDA-LDL generated high titers of antibodies with similar specificity as naturally occurring autoantibodies. Immunized animals showed a significant reduction in the extent of atherosclerotic lesions in the aortic tree after 6.5 months, compared with "saline"-immunized controls (48% vs. 68%, P < 0.005). Immunization with keyhole limpet hemocyanin produced no change in lesion formation. Although the mechanisms by which immunization led to a protective effect are unknown, these results suggest an important role for the immune system in modulating the atherogenic process and may indicate a novel approach for inhibiting the progression of atherosclerosis.
机译:动脉粥样硬化病变包含氧化的LDL(OxLDL),免疫球蛋白和具有免疫功能的细胞。在几种物种中,针对丙二醛(MDA)修饰的赖氨酸(OxLDL的抗原决定簇)的循环自身抗体水平低,并且这些自身抗体与OxLDL之间的免疫复合物存在于病变中。为了研究抗OxLDL自身抗体在动脉粥样硬化过程中的潜在作用,我们前瞻性地用同源MDA-LDL对LDL受体缺陷型兔进行了超免疫,并确定了这种干预对动脉粥样硬化发展的影响。用MDA-LDL免疫可产生高滴度的抗体,其特异性与天然存在的自身抗体相似。与“盐水”免疫的对照组相比,免疫动物在6.5个月后主动脉树中的动脉粥样硬化病变程度明显降低(48%对68%,P <0.005)。用匙孔血蓝蛋白免疫接种后,病变的形成没有改变。尽管免疫导致保护作用的机制尚不清楚,但这些结果表明免疫系统在调节动脉粥样硬化过程中起重要作用,并可能表明抑制动脉粥样硬化进展的新方法。

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