再生心脏病学的进展:干细胞与生物人工组织。

IF 3.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Jenyfer María Fuentes-Mendoza, Juan Muñoz-Moreno, Marcio Concepción-Zavaleta, Luis Concepción-Urteaga, José Paz-Ibarra, Roger Gonzales-Valdivieso, Fernanda Ginebra Castillo-Velásquez, Angie Sofía Burgos-Castillo, Regina Garza-Boullosa, Vanesa Daniela Núñez-Pérez
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引用次数: 0

摘要

背景:心血管疾病(CVD)仍然是世界范围内死亡的主要原因。人类心肌具有有限的再生能力,促使创新策略的发展,以恢复心脏功能。干细胞(SCs)和生物人工组织(bat)已成为再生心脏病学中用于心肌修复和功能恢复的有前途的工具。方法:本综述分析了目前以SC和bat为基础的CR治疗方法的临床前和临床研究,并通过综合数据库检索找到相关文献。研究评估心肌细胞分化,整合到宿主组织,血管化和机电特性。重点放在治疗潜力、安全性和转化挑战上。结果:SCs,包括胚胎干细胞和间充质干细胞,显示出分化为心肌细胞样细胞并有助于心肌修复的潜力。当与生物材料支架或去细胞化基质结合时,sc表现出更好的存活率、结构支持和功能整合。bat,如工程心脏组织,复制天然心肌结构并支持同步收缩。尽管取得了这些进展,但对免疫原性、心律失常和长期疗效的担忧仍然存在。大规模生产和个性化应用的技术障碍仍未解决。结论:SC和bat为修复受损心肌提供了创新的途径。它们的应用可能会彻底改变心力衰竭和梗死后重构的治疗策略。然而,临床翻译需要解决免疫相容性、心律失常风险和制造限制。跨学科合作和监管标准化对未来临床应用至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in regenerative cardiology: Stem cells versus bioartificial tissues.

Background: Cardiovascular disease (CVD) remains the leading cause of mortality worldwide. The human myocardium has a limited regenerative capacity, prompting the development of innovative strategies to restore cardiac function. Stem cells (SCs) and bioartificial tissues (BATs) have emerged as promising tools in regenerative cardiology for myocardial repair and functional recovery.

Methods: This review analyzes current preclinical and clinical research focused on SC- and BAT-based therapies for CR. Literature was identified through comprehensive database searches. Studies evaluating cardiomyocyte differentiation, integration into host tissue, vascularisation and electromechanical properties were selected. Emphasis was placed on therapeutic potential, safety and translational challenges.

Results: SCs, including embryonic and mesenchymal stem cells, demonstrated potential to differentiate into cardiomyocyte-like cells and contribute to myocardial restoration. When combined with biomaterial scaffolds or decellularized matrices, SCs showed improved survival, structural support, and functional integration. BATs, such as engineered heart tissue, replicated native myocardial architecture and supported synchronized contraction. Despite these advances, concerns persist regarding immunogenicity, arrhythmias, and long-term efficacy. Technical hurdles in large-scale production and personalised application remain unresolved.

Conclusions: SC- and BAT-based therapies offer innovative avenues for repairing damaged myocardium. Their application could revolutionise treatment strategies for heart failure and post-infarction remodelling. However, clinical translation requires addressing immune compatibility, arrhythmic risk and manufacturing limitations. Interdisciplinary collaboration and regulatory standardisation are essential for their future clinical adoption.

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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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