Krupnick A S, Kreisel D, Riha M, Balsara K R, Rosengard B R
Department of Surgery, Division of Cardiothoracic Surgery, Hospital of the University of Pennsylvania, 6 Silverstein Building, 3400 Spruce Street, Philadelphia, PA 19104, USA.
Curr Top Microbiol Immunol. 2004;280:139-64. doi: 10.1007/978-3-642-18846-6_4.
Ischemic cardiomyopathy leading to congestive heart failure remains the leading source of morbidity and mortality in Western society and medical management of this condition offers only palliative treatment. While allogeneic heart transplantation can both extend and improve the quality of life for patients with end-stage heart failure, this therapeutic option is limited by donor organ shortage. Even after successful transplantation, chronic cardiac rejection in the form of cardiac allograft vasculopathy can severely limit the lifespan of the transplanted organ. Current experimental efforts focus on cellular cardiomyoplasty, myocardial tissue engineering, and myocardial regeneration as alternative approaches to whole organ transplantation. Such strategies may offer novel forms of therapy to patients with end-stage heart failure within the near future.
缺血性心肌病导致的充血性心力衰竭仍是西方社会发病和死亡的主要原因,针对这种疾病的药物治疗仅提供姑息治疗。虽然同种异体心脏移植可以延长终末期心力衰竭患者的生命并提高其生活质量,但这种治疗选择受到供体器官短缺的限制。即使移植成功,心脏移植血管病变形式的慢性心脏排斥反应也会严重限制移植器官的寿命。目前的实验工作集中在细胞心肌成形术、心肌组织工程和心肌再生,作为全器官移植的替代方法。这些策略可能在不久的将来为终末期心力衰竭患者提供新的治疗形式。