心脏移植受者心肌内膜、淋巴细胞内和全血环孢素A浓度。

Ida Robertsen, Pål Falck, Arne K Andreassen, Nina K Næss, Niclas Lunder, Hege Christensen, Lars Gullestad, Anders Asberg
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引用次数: 11

摘要

背景:在心脏移植后的早期阶段,主要的挑战是减少急性排斥反应的影响。先前的研究表明,细胞内环孢素A (CsA)浓度可能是肾移植受者急性排斥反应的敏感标志物。本研究的目的是评估不同靶点CsA浓度之间的关系,作为心脏移植受者潜在的治疗药物监测(TDM)工具。方法:10名心脏移植受者(8男2女)接受基于csa的免疫抑制,纳入这项前瞻性单中心试点研究。血液样本采集每周一至两次,直至移植后12周。在每个采样时间分配一次常规活组织检查。采用高效液相色谱-质谱/质谱法测定全血、淋巴细胞内和心内膜CsA浓度。两组患者间参数评价采用Mann-Whitney U检验。为了将全血、淋巴细胞内和心内膜CsA浓度联系起来,采用线性回归分析。结果:3例患者出现轻度排斥反应。在研究期间,排斥组和无排斥组淋巴细胞内CsA谷浓度均值(范围)分别为10.1(1.5 ~ 39)和8.1 (1.3 ~ 25)ng/106个细胞(P=0.21)。相应的全血CsA浓度分别为316(153 ~ 564)和301 (152 ~ 513)ng/mL (P=0.33)。全血、淋巴细胞内、心内膜CsA浓度无相关性(P >0.11)。结论:该研究不支持淋巴细胞内CsA浓度降低与急性排斥反应之间的关联。此外,血液浓度和作用部位的浓度之间没有关联,这可能对这些患者的TDM构成挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Endomyocardial, intralymphocyte, and whole blood concentrations of ciclosporin A in heart transplant recipients.

Endomyocardial, intralymphocyte, and whole blood concentrations of ciclosporin A in heart transplant recipients.

Endomyocardial, intralymphocyte, and whole blood concentrations of ciclosporin A in heart transplant recipients.

Endomyocardial, intralymphocyte, and whole blood concentrations of ciclosporin A in heart transplant recipients.

Background: In the early phases following heart transplantation a main challenge is to reduce the impact of acute rejections. Previous studies indicate that intracellular ciclosporin A (CsA) concentration may be a sensitive acute rejection marker in renal transplant recipients. The aims of this study were to evaluate the relationships between CsA concentrations at different target sites as potential therapeutic drug monitoring (TDM) tools in heart transplant recipients.

Methods: Ten heart transplant recipients (8 men, 2 women) on CsA-based immunosuppression were enrolled in this prospective single-center pilot study. Blood samples were obtained once to twice weekly up to 12 weeks post-transplant. One of the routine biopsies was allocated to this study at each sampling time. Whole blood, intralymphocyte, and endomyocardial CsA concentrations were determined with validated HPLC-MS/MS-methods. Mann-Whitney U test was used when evaluating parameters between the two groups of patients. To correlate whole blood, intralymphocyte, and endomyocardial CsA concentrations linear regression analysis was used.

Results: Three patients experienced mild rejections. In the study period, the mean (range) intralymphocyte CsA trough concentrations were 10.1 (1.5 to 39) and 8.1 (1.3 to 25) ng/106 cells in the rejection and no-rejection group, respectively (P=0.21). Corresponding whole blood CsA concentrations were 316 (153 to 564) and 301 (152 to 513) ng/mL (P=0.33). There were no correlations between whole blood, intralymphocyte, or endomyocardial concentrations of CsA (P >0.11).

Conclusions: The study did not support an association between decreasing intralymphocyte CsA concentrations and acute rejections. Further, there were no association between blood concentrations and concentrations at sites of action, potentially challenging TDM in these patients.

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