调节性 T 细胞作为急性心肌梗死的治疗靶点

IF 3.2 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular immunology Pub Date : 2024-06-11 DOI:10.1016/j.molimm.2024.06.003
QiHong Wu , Mengyue Wu , Kun Zhang , Ran Sun , Hong Li , Jiyu Tong , Yingkun Guo
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引用次数: 0

摘要

急性心肌梗死(AMI)主要由血管闭塞或血栓形成引发,是所有心血管疾病中发病率和死亡率最高的原因。炎症所涉及的复杂细胞过程进一步加剧了急性心肌梗死的破坏性后果。在过去二十年中,许多研究报告称,调节性 T 细胞(Tregs)作为主要的免疫调节细胞,在急性心肌梗死的进展过程中发挥着至关重要的作用。本综述全面探讨了调节性 T 细胞与 AMI 发展之间错综复杂的关系。此外,它还探讨了以Tregs及其外泌体为重点的新兴治疗策略。此外,我们还强调了采用非侵入性体内成像技术推动基于 Tregs 的 AMI 治疗临床应用的重要性。尽管进一步的研究对全面阐明Tregs作用的分子机制至关重要,但针对这些细胞的疗法在治疗AMI患者方面潜力巨大。
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Regulatory T cells as a therapeutic target in acute myocardial infarction

Acute myocardial infarction (AMI), mainly triggered by vascular occlusion or thrombosis, is the most prevalent cause of morbidity and mortality among all cardiovascular diseases. The devastating consequences of AMI are further aggravated by the intricate cellular processes involved in inflammation. In the past two decades, many studies have reported that regulatory T cells (Tregs), as the main immunoregulatory cells, play a crucial role in AMI progression. This review offers a comprehensive insight into the intricate relationship between Tregs and AMI development. Moreover, it explores emerging therapeutic strategies that focus on Tregs and their exosomes. Furthermore, we underscore the importance of employing noninvasive in vivo imaging techniques to advance the clinical applications of Tregs-based treatments in AMI. Although further research is essential to fully elucidate the molecular mechanisms underlying the effects of Tregs, therapies tailored to these cells hold immense potential for the treatment of patients with AMI.

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来源期刊
Molecular immunology
Molecular immunology 医学-免疫学
CiteScore
6.90
自引率
2.80%
发文量
324
审稿时长
50 days
期刊介绍: Molecular Immunology publishes original articles, reviews and commentaries on all areas of immunology, with a particular focus on description of cellular, biochemical or genetic mechanisms underlying immunological phenomena. Studies on all model organisms, from invertebrates to humans, are suitable. Examples include, but are not restricted to: Infection, autoimmunity, transplantation, immunodeficiencies, inflammation and tumor immunology Mechanisms of induction, regulation and termination of innate and adaptive immunity Intercellular communication, cooperation and regulation Intracellular mechanisms of immunity (endocytosis, protein trafficking, pathogen recognition, antigen presentation, etc) Mechanisms of action of the cells and molecules of the immune system Structural analysis Development of the immune system Comparative immunology and evolution of the immune system "Omics" studies and bioinformatics Vaccines, biotechnology and therapeutic manipulation of the immune system (therapeutic antibodies, cytokines, cellular therapies, etc) Technical developments.
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