首页> 美国卫生研究院文献>Tissue Engineering. Part A >Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement
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Early Systemic Cellular Immune Response in Children and Young Adults Receiving Decellularized Fresh Allografts for Pulmonary Valve Replacement

机译:接受脱细胞新鲜同种异体肺动脉瓣置换术的儿童和青少年的早期全身细胞免疫反应。

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摘要

>Objectives: The longevity of homografts is determined by the activation of the recipients' immune system resulting from allogenic antigen exposition. Fresh decellularized pulmonary homografts (DPH) have shown promising early results in pulmonary valve replacement in children and young adults and could potentially avoid significant activation of the immune system, as more than 99% of the donor DNA is removed during the decellularization process. While the humoral immune response to decellularized allografts has been studied, detailed information on the more significant cellular immune response is currently lacking.>Methods and Results: Peripheral blood samples were obtained from patients undergoing pulmonary valve replacement with DPH before, after, and for approximately 3 years after implantation. Absolute counts and percentages of mature T- (CD3+), B- (CD19+), and natural killer- (CD16+/CD56+) cells, as well as T helper- (CD4+) and cytotoxic T-cell- (CD8+) subsets, were determined by fluorescence-activated cell sorting (FACS). Between May 2009 and September 2013, 199 blood samples taken from 47 patients with a mean age at DPH implantation of 16.6±10.8 years were analyzed. The hemodynamic performance of DPH was excellent in all but one patient, and no valve-related deaths or conduit explantations were observed. The short-term follow up revealed a significant postoperative decrease in cell counts of most subtypes with reconstitution after 3 months. Continued assessment did not show any significant deviations in cell counts from their baseline values.>Conclusion: The absence of cellular immune response in patients receiving DPH supports the concept that decellularization can provide a basis for autologous regeneration.
机译:>目标:同种异体移植物的寿命取决于同种异体抗原暴露引起的受体免疫系统的激活。新鲜的脱细胞肺同种异体移植物(DPH)已显示出在儿童和年轻人中进行肺动脉瓣置换的有希望的早期结果,并可能避免免疫系统的显着激活,因为在脱细胞过程中会去除超过99%的供体DNA。虽然已经研究了对脱细胞同种异体移植物的体液免疫反应,但目前仍缺乏有关更重要的细胞免疫反应的详细信息。>方法和结果:从接受DPH肺动脉瓣置换术的患者外周血样本,植入后以及植入后约3年。成熟T-(CD3 + ),B-(CD19 + )和自然杀手-(CD16 + / CD56)的绝对计数和百分比 + )细胞,T辅助细胞(CD4 + )和细胞毒性T细胞-(CD8 + )亚组的测定方法如下:荧光激活细胞分选(FACS)。在2009年5月至2013年9月之间,分析了47位平均DPH植入时间为16.6±10.8岁的患者的199份血液样本。除一名患者外,DPH的血液动力学性能均极佳,未观察到与瓣膜相关的死亡或导管植入。短期随访显示,术后3个月,大多数亚型的患者术后细胞计数均明显下降。继续进行的评估并未显示出细胞计数与其基线值有任何显着差异。>结论:接受DPH的患者缺乏细胞免疫应答,支持脱细胞可以为自体再生提供基础的概念。

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