Shah Syed Raza, Abbasi Zainab, Fatima Mazia, Ochani Rohan Kumar, Shahnawaz Waqas, Asim Khan Muhammad, Shah Syed Arbab
North Florida Regional Medical Center, University of Central Florida (Gainesville), Gainesville, FL, USA.
Department of Internal Medicine, Dow University of Health Sciences (DUHS), Karachi, Pakistan.
J Community Hosp Intern Med Perspect. 2018 Feb 6;8(1):21-22. doi: 10.1080/20009666.2018.1428023. eCollection 2018.
IL-1 cytokines are mainly responsible for controlling a series of pro-inflammatory reactions induced in response to pathogen mediated tissue injury. Among the IL-1 cytokine family, IL-1 β results in upregulation of genes responsible for boosting immune system reactivity and inflammatory response. With growing pathophysiological relevance of IL-1β in a myriad of disease pathogenesis, new biological drugs have been developed in recent years. One such drug, Canakinumab, targeting IL-1β has been recently approved for clinical use. The recent results from the CANTOS (Canakinumab Anti-Inflammatory Thrombosis Outcome Study) trial are encouraging in this aspect. The results suggest that anti-inflammatory therapy using canakinumab at a dose of 150 mg every 3 months led to significantly lower recurrent cardiovascular events than the placebo drug. These results were independent of lipid-lowering effects of these drugs. If the results are widely applicable, the CANTOS trial would reaffirm the hypothesis of atherothrombosis due to inflammation, hence supporting the need for a cytokine-based therapy for the secondary prevention of cardiovascular diseases. Moreover, the potential benefits of the phenomenal reduction in the inflammatory cascade induced by canakinumab should be carefully balanced against its long-term safety profile which is yet unknown. However, the inflammatory hypothesis of atherothrombosis supports a cytokine-based therapy for the secondary prevention of cardiovascular disease. Furthermore, the potential benefits from the reduction in inflammatory markers induced by canakinumab should be carefully balanced against its unknown long-term safety profile.
白细胞介素-1细胞因子主要负责控制因病原体介导的组织损伤而引发的一系列促炎反应。在白细胞介素-1细胞因子家族中,白细胞介素-1β会导致负责增强免疫系统反应性和炎症反应的基因上调。随着白细胞介素-1β在众多疾病发病机制中的病理生理相关性不断增加,近年来已开发出新型生物药物。其中一种药物,即靶向白细胞介素-1β的卡那单抗,最近已获批用于临床。在这方面,卡那单抗抗炎血栓形成结果研究(CANTOS)试验的最新结果令人鼓舞。结果表明,每3个月使用150毫克卡那单抗进行抗炎治疗导致复发性心血管事件显著低于安慰剂药物。这些结果与这些药物的降脂作用无关。如果这些结果具有广泛适用性,CANTOS试验将再次证实炎症导致动脉粥样硬化血栓形成的假说,从而支持基于细胞因子的疗法用于心血管疾病二级预防的必要性。此外,卡那单抗引起的炎症级联反应显著降低所带来的潜在益处,应与尚不清楚的长期安全性进行仔细权衡。然而,动脉粥样硬化血栓形成的炎症假说支持基于细胞因子的疗法用于心血管疾病的二级预防。此外,卡那单抗引起的炎症标志物降低所带来的潜在益处,应与尚不清楚的长期安全性进行仔细权衡。