Modulating Autoimmunity against LDL: Development of a Vaccine against Atherosclerosis

被引:6
作者
Marchini, Timoteo [1 ,2 ,3 ,4 ,5 ]
Abogunloko, Tijani [1 ,2 ,3 ,5 ]
Wolf, Dennis [1 ,2 ,3 ]
机构
[1] Univ Freiburg, Univ Heart Ctr, Cardiol & Angiol 1, Hugstetter Str 55, D-79106 Freiburg, Germany
[2] Univ Freiburg, Med Ctr, Freiburg, Germany
[3] Univ Freiburg, Fac Med, Freiburg, Germany
[4] Univ Buenos Aires, CONICET, Fac Farm & Bioquim, Inst Bioquim & Med Mol IBIMOL, Buenos Aires, DF, Argentina
[5] Univ Freiburg, Spemann Grad Sch Biol & Med SGBM, Freiburg, Germany
来源
HAMOSTASEOLOGIE | 2021年 / 41卷 / 06期
基金
欧洲研究理事会;
关键词
atherosclerosis; vaccination; T cells; antibodies; autoimmunity; REGULATORY T-CELLS; OXIDIZED LDL; VASCULAR INFLAMMATION; INFLUENZA VACCINATION; PEPTIDE SEQUENCES; AORTIC LESIONS; DEFICIENT MICE; HEART-DISEASE; IN-VIVO; IMMUNIZATION;
D O I
10.1055/a-1661-1908
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis is a chronic inflammatory disease of the arterial wall that leads to the build-up of occluding atherosclerotic plaques. Its clinical sequelae, myocardial infarction and stroke, represent the most frequent causes of death worldwide. Atherosclerosis is a multifactorial pathology that involves traditional risk factors and chronic low-grade inflammation in the atherosclerotic plaque and systemically. This process is accompanied by a strong autoimmune response that involves autoreactive T cells in lymph nodes and atherosclerotic plaques, as well as autoantibodies that recognize low-density lipoprotein (LDL) and its main protein component apolipoprotein B (ApoB). In the past 60 years, numerous preclinical observations have suggested that immunomodulatory vaccination with LDL, ApoB, or its peptides has the potential to specifically dampen autoimmunity, enhance tolerance to atherosclerosis-specific antigens, and protect from experimental atherosclerosis in mouse models. Here, we summarize and discuss mechanisms, challenges, and therapeutic opportunities of immunomodulatory vaccination and other strategies to enhance protective immunity in atherosclerosis.
引用
收藏
页码:447 / 457
页数:11
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