Heart and Vascular Centre, Semmelweis University, 68 Varosmajor Street, Budapest, 1122 - Hungary.
Heart and Vascular Centre, Semmelweis University, 68 Varosmajor Street, Budapest, 1122 - Hungary.
Transpl Immunol. 2023 Aug;79:101853. doi: 10.1016/j.trim.2023.101853. Epub 2023 May 16.
Despite novel immunosuppressive (IS) protocols, adverse effects of IS drugs continue to have notable negative impact on patient and cardiac allograft survival after heart transplantation (HTx). Therefore, IS regimens with less toxic side effects are sorely needed. We aimed to evaluate the efficacy of extracorporeal photopheresis (ECP) in combination with tacrolimus-based maintenance IS therapy in the treatment of allograft rejection in adult HTx recipients. Indications for ECP included acute moderate-to-severe or persistent mild cellular rejection, or mixed rejection. Twenty-two patients underwent a median of 22(2-44) ECP treatments after HTx. Median duration of ECP course was 173.5(2-466) days. No relevant adverse effects of ECP were noted. Reduction of methylprednisolone doses was safe throughout the ECP course. ECP, used in conjunction with pharmacological anti-rejection therapy, had a successful reversal of cardiac allograft rejection, decreased the rates of subsequential rejection episodes and normalized the allograft function in patients completing the ECP course. Short- and long-term survivals were excellent (91% at 1 and 5 years post-ECP) and comparable to International Society for Heart and Lung Transplantation registry data on HTx recipient overall survival. In conclusion, ECP can be safely used for the treatment and prevention of cardiac allograft rejection in conjunction with traditional IS regimen.
尽管采用了新型免疫抑制(IS)方案,但 IS 药物的不良反应仍然对心脏移植(HTx)后患者和心脏移植物的存活产生显著的负面影响。因此,非常需要具有较少毒性副作用的 IS 方案。我们旨在评估体外光化学疗法(ECP)联合他克莫司为基础的维持性 IS 治疗在成人 HTx 受者同种异体移植排斥反应治疗中的疗效。ECP 的适应证包括急性中度至重度或持续轻度细胞性排斥反应,或混合性排斥反应。22 例患者在 HTx 后中位数接受了 22(2-44)次 ECP 治疗。ECP 疗程的中位数持续时间为 173.5(2-466)天。未观察到 ECP 的相关不良反应。在整个 ECP 疗程中,减少甲泼尼龙剂量是安全的。ECP 与药物抗排斥治疗联合使用,成功逆转了心脏移植物排斥反应,降低了随后排斥反应发作的发生率,并使完成 ECP 疗程的患者的移植物功能恢复正常。短期和长期存活率均极佳(ECP 后 1 年和 5 年分别为 91%),与国际心肺移植学会 HTx 受者总生存率登记数据相当。总之,ECP 可与传统 IS 方案联合安全用于治疗和预防心脏移植物排斥反应。