Ludwig Bernd, Schneider Johanna, Föll Daniela, Zhou Qian
Department of Cardiology and Angiology I, Heart Center Freiburg University, Faculty of Medicine, University of Freiburg, Germany.
Department of Nephrology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Eur Heart J Case Rep. 2020 Jan 25;4(1):1-4. doi: 10.1093/ehjcr/ytz246. eCollection 2020 Feb.
Antibody-mediated rejection (AMR) in cardiac transplantation may manifest early within the first weeks after transplantation but also late after months to years following transplantation resulting in mild heart failure to cardiogenic shock. While patients with early cardiac AMR are less affected and seem to have survival rates comparable to transplant recipients without AMR, late cardiac AMR is frequently associated with graft dysfunction, fulminant forms of cardiac allograft vasculopathy, and a high mortality rate. Nevertheless, AMR of cardiac allografts remains difficult to diagnose and to treat.
We report the case of a 47-year-old male patient with late AMR of the cardiac allograft 3 years after heart transplantation. Antibody-mediated rejection was confirmed by endomyocardial biopsy and the presence of donor-specific antibodies (DSA). The patient was treated with high dose of prednisolone, plasmapheresis, intravenous Gamma Globulin, rituximab, immunoadsorption, and bortezomib. Under this treatment regimen left ventricular ejection fraction and pro B-type natriuretic peptide recovered, and the patient improved to New York Heart Association Class I. Currently, 3 years after the diagnosis of cardiac AMR, graft function continues to be nearly normal, and there is no evidence for transplant vasculopathy.
This case illustrates that AMR can occur at any time after transplantation. Although graft function fully recovered after treatment in our patient, the level of DSA remained high, suggesting that DSA may not be a reliable parameter to determine the intensity and duration of the therapy.
心脏移植中的抗体介导性排斥反应(AMR)可能在移植后的头几周内早期出现,也可能在移植数月至数年之后晚期出现,导致从轻度心力衰竭到心源性休克等不同情况。虽然早期心脏AMR患者受影响较小,其生存率似乎与无AMR的移植受者相当,但晚期心脏AMR常与移植物功能障碍、暴发性心脏同种异体血管病变以及高死亡率相关。尽管如此,心脏同种异体移植的AMR仍然难以诊断和治疗。
我们报告了一例47岁男性患者,在心脏移植3年后发生了晚期心脏同种异体移植AMR。经心内膜心肌活检及供者特异性抗体(DSA)检测确诊为抗体介导性排斥反应。该患者接受了大剂量泼尼松龙、血浆置换、静脉注射丙种球蛋白、利妥昔单抗、免疫吸附和硼替佐米治疗。在这种治疗方案下,左心室射血分数和前B型利钠肽恢复正常,患者病情改善至纽约心脏协会I级。目前,在诊断心脏AMR 3年后,移植物功能仍接近正常,且无移植血管病变的证据。
该病例表明AMR可在移植后的任何时间发生。虽然我们的患者在治疗后移植物功能完全恢复,但DSA水平仍然很高,这表明DSA可能不是确定治疗强度和持续时间的可靠参数。