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心血管疾病中的预测性和保护性自身免疫:疫苗疗法能否成为现实?

Predictive and protective autoimmunity in cardiovascular diseases: is vaccination therapy a reality?

作者信息

Toubi E, Shoenfeld Y

机构信息

Division of Allergy and Clinical Immunology, Bnai Zion Medical Center, Haifa, Israel.

出版信息

Lupus. 2005;14(9):665-9. doi: 10.1191/0961203305lu2196oa.

Abstract

The role of the immune system in modulating atherosclerosis has recently been well documented. Studies have revealed that cellular and humoral immunity plays crucial roles in atherogenic plaque formation. This includes macrophages, CD4+ T cells and dendritic cells as well as autoantigens such as oxidized low density lipoprotein (oxLDL), heat shock proteins and beta2-glycoprotein I. Given these recent advances, various modifications of the immune system in experimental models have been proposed as therapeutic strategies, with the potential of inhibiting atherosclerosis progression. These modifications are switching the immune system (CD4+ T cells) from Th1 towards a Th2 anti-inflammatory cytokine secretion, and the induction of protective antibodies both of which may be induced by specific vaccination. Recent identification of specific immunoreactive antigenic epitopes on modified LDL, their successful implementation for immunization and the induction of atheroprotection, supports the idea that active vaccination may emerge as a novel immuno-modulating atheroprotective strategy.

摘要

免疫系统在调节动脉粥样硬化中的作用最近已有充分记录。研究表明,细胞免疫和体液免疫在动脉粥样硬化斑块形成中起着关键作用。这包括巨噬细胞、CD4 + T细胞和树突状细胞以及自身抗原,如氧化型低密度脂蛋白(oxLDL)、热休克蛋白和β2-糖蛋白I。鉴于这些最新进展,在实验模型中对免疫系统进行的各种修饰已被提议作为治疗策略,具有抑制动脉粥样硬化进展的潜力。这些修饰包括将免疫系统(CD4 + T细胞)从Th1转变为分泌Th2抗炎细胞因子,以及诱导保护性抗体,这两者都可以通过特定疫苗接种来诱导。最近在修饰的低密度脂蛋白上鉴定出特定的免疫反应性抗原表位,它们在免疫接种中的成功应用以及动脉粥样硬化保护作用的诱导,支持了主动疫苗接种可能成为一种新型免疫调节性动脉粥样硬化保护策略的观点。

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