Department of Nephrology and Kidney Transplantation, Hospital Clinic de Barcelona, Barcelona, Spain.
Laboratori Experimental de Nefrologia i Trasplantament (LENIT), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Transpl Int. 2023 Jan 12;36:10840. doi: 10.3389/ti.2023.10840. eCollection 2023.
Extracorporeal photopheresis (ECP) is an immunomodulatory therapy based on the infusion of autologous cellular products exposed to ultraviolet light (UV) in the presence of a photosensitizer. The study evaluates the ECP efficacy as induction therapy in a full-mismatch kidney transplant rat model. Dark Agouti to Lewis (DA-L) kidney transplant model has been established. ECP product was obtained from Lewis rat recipients after DA kidney graft transplantation (Lew). Leukocytes of those Lew rats were exposed to 8-methoxy psoralen, and illuminated with UV-A. The ECP doses assessed were 10 × 10 and 100 × 10 cells/time point. Lewis recipients received seven ECP infusions. DA-L model was characterized by the appearance of donor-specific antibodies (DSA) and kidney function deterioration from day three after kidney transplant. The dysfunction progressed rapidly until graft loss (6.1 ± 0.5 days). Tacrolimus at 0.25 mg/kg prolonged rat survival until 11.4 ± 0.7 days ( = 0.0004). In this context, the application of leukocytes from LewDA sensitized rats accelerated the rejection (8.7 ± 0.45, = 0.0012), whereas ECP product at high dose extended kidney graft survival until 26.3 ± 7.3 days, reducing class I and II DSA in surviving rats. ECP treatment increases kidney graft survival in full-mismatch rat model of acute rejection and is a suitable immunomodulatory therapy to be explored in kidney transplantation.
体外光分离术(ECP)是一种基于在光敏剂存在下将自体细胞产物暴露于紫外光(UV)以进行免疫调节的治疗方法。本研究评估了 ECP 在完全错配肾移植大鼠模型中作为诱导治疗的疗效。已建立了深棕褐色到刘易斯(DA-L)肾移植模型。从 DA 肾移植后接受Lew 治疗的 Lewis 大鼠中获得 ECP 产品。这些 Lew 大鼠的白细胞暴露于 8-甲氧基补骨脂素,并接受 UV-A 照射。评估的 ECP 剂量为 10×10 和 100×10 个细胞/时间点。Lewis 受者接受了 7 次 ECP 输注。DA-L 模型的特征是出现供体特异性抗体(DSA)和肾移植后第三天肾功能恶化。肾功能迅速恶化,直至移植物丢失(6.1±0.5 天)。环孢素 A(Tacrolimus)0.25mg/kg 将大鼠的存活时间延长至 11.4±0.7 天(=0.0004)。在这种情况下,LewDA 致敏大鼠的白细胞的应用加速了排斥反应(8.7±0.45,=0.0012),而高剂量的 ECP 产品延长了肾移植物的存活时间,直至 26.3±7.3 天,减少了存活大鼠的 I 类和 II 类 DSA。ECP 治疗可增加完全错配大鼠急性排斥模型中肾移植物的存活率,是一种适合在肾移植中探索的免疫调节治疗方法。