Institute for Cardiovascular Prevention (IPEK), CRC 1123 Atherosclerosis - Mechanisms and Networks of novel therapeutic Targets, Ludwig-Maximilians-Universität, Ludwig-Maximilians-University Munich, Pettenkoferstraße 9, Munich 80336, Germany.
Department of Medical Biochemistry, Amsterdam University Medical Centers, Location AMC, Amsterdam Cardiovascular Sciences (ACS), University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, the Netherlands.
Eur Heart J. 2019 Dec 21;40(48):3937-3946. doi: 10.1093/eurheartj/ehz283.
The outcomes of the Canakinumab Anti-inflammatory Thrombosis Outcome Study (CANTOS) trial have unequivocally proven that inflammation is a key driver of atherosclerosis and that targeting inflammation, in this case by using an anti-interleukin-1β antibody, improves cardiovascular disease (CVD) outcomes. This is especially true for CVD patients with a pro-inflammatory constitution. Although CANTOS has epitomized the importance of targeting inflammation in atherosclerosis, treatment with canakinumab did not improve CVD mortality, and caused an increase in infections. Therefore, the identification of novel drug targets and development of novel therapeutics that block atherosclerosis-specific inflammatory pathways and exhibit limited immune-suppressive side effects, as pursued in our collaborative research centre, are required to optimize immunotherapy for CVD. In this review, we will highlight the potential of novel immunotherapeutic targets that are currently considered to become a future treatment for CVD.
Canakinumab 抗炎性血栓结局研究(CANTOS)的结果明确证实,炎症是动脉粥样硬化的一个关键驱动因素,通过使用抗白细胞介素-1β 抗体靶向炎症可以改善心血管疾病(CVD)的结局。对于具有促炎体质的 CVD 患者尤其如此。虽然 CANTOS 强调了靶向动脉粥样硬化炎症的重要性,但使用卡那奴单抗治疗并未改善 CVD 死亡率,并导致感染增加。因此,需要识别新的药物靶点,并开发新的治疗方法,阻断动脉粥样硬化特异性炎症途径,同时表现出有限的免疫抑制副作用,正如我们的合作研究中心所追求的那样,以优化 CVD 的免疫治疗。在这篇综述中,我们将重点介绍目前被认为是 CVD 未来治疗方法的新型免疫治疗靶点的潜力。