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Ischemic cardiomyopathy: Pathological Findings In A Case Of Stem Cell Implantation

机译:缺血性心肌病:干细胞植入病例的病理学发现

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The term “regenerative medicine” is a multidisciplinary field involving molecular and cell biologist, embryologist, pathologist, clinicians, bioengineers, and not to exclude ethicists. Early clinical studies, so for have indicate that, a stem cell implantation is feasible and has beneficial effect on infarcted heart. When compared to death of donor hearts for transplantation, complications associated with immunosupression, long-term failure of transplanted organs with high morbidity and mortality rates associated with myocardial infarction, stem cells scores over organ transplant. Most of the trials to date assessed cardiac function at 4-6 months after treatment and long-term outcome have not yet been described. Here in we present histopathological findings in explanted heart in a 50-year-old male patient who had received stem cell therapy for chronic ischemic heart disease. Introduction Stem cell therapy is emerging as a potential therapy for infarcted heart. There is growing interest in clinical cardiology treating patients with myocardial infarction or cardiac failure with stem cells. Cardiac experiments, mainly with adult homologous stem cells, have proved that this therapy is safe and may improve myocardial vascularization and pump function.1 Stem cells are multipotent, undifferentiated cells capable of multiplication and differentiation. Four categories of stem cells have been examined for their ability to promote cardiac repair: bone marrow derived/circulating progenitor cells (BMPCs) and their subpopulation, skeletal myoblasts (SM), embryonic stem cells (ESCs) and resident cardiac stem (or cardiomyocyte progenetor) cells (CMPCs).2 Skeletal muscle cells and BMPCs are being used in clinical trials mainly because these cell types are potentially autologous. ESCs are at present the major heterologous source of cells being considered and ethically the most sensitive as their derivation requires the destruction of early human embryos. Different techniques and routes of administering stem cells have been advocated. Although intramyocardial injection process is simple and can be performed by direct inspection of the potential target zones during cardiac surgery, it is associated with intraoperative and postoperative risks.3 Intracoronary injection has advantage because it can deliver the maximum concentration of cells to the site of infarct and peri-infarct tissue during the first passage. However, in successive days intravenous administration of stem cells will be an attractive and practical mode of delivery. There exists always a risk of micro vascular obliteration and of poor therapeutic efficiency if the stem cells are to cross the coronary wall and migrate extravascularly- especially when targeting a territory supplied by occluded coronary arteries.1 While experimental studies and early phase clinical trials tend to support that stem cell therapy enhances cardiac repair by improving myocardial vascularization and pump function. Present consensus is that stem cell have therapeutic benefit, but this is not based on the ability of these cells to Tran differentiate into cardiac myocytes. There are still several key issues still needs to be addressed like; the optimal type of donor cells in relation to the clinical profile, the mechanism by which cell engraftment improves cardiac function, development of less invasive cell delivery techniques and relevance to non-ischemic heart failure.2 Case Report He was a 50-year-old male, diabetic since 18 years old, hypertensive, and a known case of coronary artery disease. This patient had under gone coronary artery bypass graft (CABG) for triple vessel disease, with 4 grafts in 2005 in our hospital. Later, he was admitted with repeated signs of ischemia. He was offered a choice of stem cell therapy in 2006. He subsequently under went stem cell therapy in 2006. Autologous stem cells were harvested from bone marrow. Stem cell injection was done through left coronary artery, right coronary
机译:术语“再生医学”是一个涉及分子和细胞生物学家,胚胎学家,病理学家,临床医生,生物工程师的跨学科领域,并不排除伦理学家。因此,早期的临床研究表明,干细胞植入是可行的,并且对梗塞的心脏具有有益的作用。与用于移植的供体心脏的死亡,与免疫抑制相关的并发症,具有高发病率的移植器官的长期衰竭以及与心肌梗塞相关的死亡率相比,干细胞得分高于器官移植。迄今为止,大多数试验尚未评估治疗后4-6个月的心功能和长期预后。在这里,我们介绍了一位接受慢性干性心脏病干细胞治疗的50岁男性患者的移植心脏的组织病理学发现。简介干细胞疗法正在成为一种潜在的梗塞性心脏病疗法。用干细胞治疗患有心肌梗塞或心力衰竭的患者的临床心脏病学越来越受到关注。心脏实验,主要是成人成体同源干细胞,已证明该疗法是安全的,可改善心肌血管形成和泵功能。1干细胞是能繁殖和分化的多能,未分化细胞。已检查了四类干细胞促进心脏修复的能力:骨髓衍生/循环祖细胞(BMPC)及其亚群,骨骼成肌细胞(SM),胚胎干细胞(ESC)和常驻心脏干(或心肌祖细胞) 2)骨骼肌细胞和BMPC正在临床试验中使用,主要是因为这些细胞类型可能是自体的。目前,ESCs被认为是细胞的主要异源来源,并且在伦理上最敏感,因为它们的衍生需要破坏早期人类胚胎。已经提出了干细胞施用的不同技术和途径。尽管心肌内注射过程很简单,并且可以在心脏手术期间直接检查潜在的目标区域来进行,但它与术中和术后风险相关。3冠状动脉内注射具有优势,因为它可以将最大浓度的细胞输送到梗死部位。以及第一次通过时的梗塞周围组织。然而,在连续的几天中,干细胞的静脉内给药将是有吸引力且实用的递送方式。如果干细胞穿过冠状动脉壁并在血管外迁移,特别是当靶向由闭塞的冠状动脉提供的区域时,总会存在微血管闭塞和治疗效果差的风险。1尽管实验研究和早期临床试验倾向于支持干细胞疗法通过改善心肌血管形成和泵功能来增强心脏修复。目前的共识是干细胞具有治疗作用,但这不是基于这些细胞Tran分化为心肌细胞的能力。仍然有一些关键问题需要解决,例如:与临床特征有关的最佳供体细胞类型,细胞植入改善心脏功能的机制,侵入性较小的细胞递送技术的发展以及与非缺血性心力衰竭的相关性。2病例报告他现年50岁男性,自18岁起患有糖尿病,高血压和已知的冠状动脉疾病病例。该患者因三支血管疾病而接受了冠状动脉旁路移植术(CABG),2005年在我院进行了4例移植。后来,他被接纳患有反复缺血的迹象。 2006年为他提供了干细胞治疗的选择。随后,他在2006年接受了干细胞治疗。自体干细胞是从骨髓中获得的。通过左冠状动脉,右冠状动脉进行干细胞注射

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