Costimulatory and Coinhibitory Immune Checkpoints in Atherosclerosis Therapeutic Targets in Atherosclerosis?

被引:4
|
作者
Nitz, Katrin [1 ]
Herrmann, Joerg [1 ]
Lerman, Amir [1 ]
Lutgens, Esther [1 ,2 ]
机构
[1] Mayo Clin, Dept Cardiovasc Med, Rochester, MN USA
[2] Mayo Clin, Dept Immunol, Rochester, MN USA
来源
JACC-BASIC TO TRANSLATIONAL SCIENCE | 2024年 / 9卷 / 06期
关键词
atherosclerosis; coinhibition; costimulation; immune system; inflammation; CELL CO-STIMULATION; REGULATORY T-CELLS; REDUCES ATHEROSCLEROSIS; PREVENTS ATHEROSCLEROSIS; RHEUMATOID-ARTHRITIS; PLAQUE INFLAMMATION; ANTITUMOR IMMUNITY; ENDOTHELIAL-CELLS; DENDRITIC CELLS; CD40; LIGAND;
D O I
10.1016/j.jacbts.2023.12.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The bene fits of current state-of-the-art treatments to combat atherosclerotic cardiovascular disease (ASCVD) have stagnated. Treatments are mostly based on controlling cardiovascular risk factors, especially hyperlipidemia. Although the most recent advances with PCSK-9 inhibitors support the hyperlipidemia aspect of ASCVD, several lines of experimental evidence have outlined that atherosclerosis is also driven by in flammation. In the past years, phase 1, 2, and 3 clinical trials targeting in flammation to combat ASCVD have revealed that patients do tolerate such immune therapies, show decreases in in flammatory markers, and/or have reductions in cardiovascular endpoints. However, the search for the optimal anti-in flammatory or immune-modulating strategy and the strati fication of patients who would bene fit from such treatments and appropriate treatment regimens to combat ASCVD is only just beginning. In this review, we focus on immune checkpoint -based therapeutics (costimulation and coinhibition), many of which are already approved by the U.S. Food and Drug Administration for the treatment of cancer or autoimmune diseases, and discuss their use as a novel immunotherapeutic strategy to treat ASCVD. (J Am Coll Cardiol Basic Trans Science 2024;9:827 -843) (c) 2024 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:827 / 843
页数:17
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