Inflammatory Causes and Immunotherapy Potential in Cardiovascular Diseases Treatment

Shijie Zhou, Lidong Zhai, Zhai L. Cardiolog, Res Cardiovasc
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Abstract

Inflammatory profile in the cardiovascular diseases has been acknowledged widely; yet the potential of immunotherapy in the treatment of cardiovascular diseases (CVD) is not fully met. The primary and secondary inflammatory risk factors of CVD; as well as drivers of atherosclerosis from the immune system are elaborated in this review. The approaches to treat CVD in respect of immunotherapy focus on targeting cytokine response pathways; novel engineering cytokines and superkines; and targeting specialized pro-resolving mediators (SPMs) in atherosclerosis. Immunotherapy in the treatment of heart failure has gained great advancement in targeting heart fibrosis to stop and even reverse cardiac remodeling. With a deeper understanding of the roles T cells and macrophages in the development of fibrosis in heart failure; harnessing them became possible to treat heart failure. T-cell therapy with chimeric antigen receptor (CAR T-cell); as well as CRISPR gene editing therapy make personalized diagnosis and treatment possible and bring a lot of hope to concur this debilitating disease. This review attempts to summarize new understandings of inflammatory mechanisms underlying CVD and major advancements as well as challenges in CVD immunotherapy with a hope to offer a perspective on strategies to advance future therapies.
心血管疾病治疗中的炎症原因和免疫治疗潜力
心血管疾病的炎症特征已得到广泛认可;然而,免疫疗法在治疗心血管疾病(CVD)方面的潜力尚未完全得到满足。CVD的原发性和继发性炎症危险因素;以及来自免疫系统的动脉粥样硬化驱动因素在这篇综述中进行了阐述。在免疫疗法方面治疗CVD的方法侧重于靶向细胞因子反应途径;新型工程细胞因子和超细胞因子;以及在动脉粥样硬化中靶向专门的促分解介质(SPMs)。免疫疗法在治疗心力衰竭方面取得了巨大进展,靶向心脏纤维化以阻止甚至逆转心脏重塑。对T细胞和巨噬细胞在心力衰竭纤维化发展中的作用有了更深入的了解;利用它们治疗心力衰竭成为可能。用嵌合抗原受体(CAR T细胞)进行T细胞治疗;以及CRISPR基因编辑疗法使个性化诊断和治疗成为可能,并为治疗这种使人衰弱的疾病带来了很大的希望。这篇综述试图总结对心血管疾病炎症机制的新理解,以及心血管疾病免疫疗法的主要进展和挑战,希望为推进未来治疗的策略提供一个视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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