Successful Desensitization with Imlifidase and Daratumumab in a Highly Immunized, Crossmatch Positive, Blood Group-Incompatible Living-Donor Re-Transplant Recipient with Systemic Lupus Erythematosus and Antiphospholipid Syndrome

E. Schrezenmeier, Mira Choi, B. Globke, Thomas Dörner, Alexandra Leimbach, B. Osmanodja, Alexander Schramm, Kerstin Amann, K. Eckardt, K. Budde, Robert Öllinger, N. Lachmann, F. Halleck
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Abstract

Introduction: The transplantation of highly sensitized patients remains a major obstacle. Immunized patients wait longer for a transplant if not prioritized, and if transplanted, their transplant outcome is worse. Case Presentation: We report a successful AB0- and HLA-incompatible living donor kidney transplantation in a 35-year-old female patient with systemic lupus erythematosus (SLE) and antiphospholipid syndrome. The patient had a positive T- and B-cell complement-dependent cytotoxicity (CDC) crossmatch and previous graft loss due to renal vein thrombosis. We treated the patient with intravenous immunoglobulins, rituximab, horse anti-thymocyte globulin, daratumumab, and imlifidase, besides standard immunosuppression. All IgG antibodies were sensitive to imlifidase treatment. Besides donor-specific HLA antibodies, anti-dsDNA antibodies and antiphospholipid antibodies were cleaved. The patient initially had delayed graft function. Two kidney biopsies (day 7 and day 14) revealed acute tubular necrosis without signs of HLA antibody-mediated rejection. On posttransplant day 30, hemodialysis was stopped, and creatinine levels declined over the next weeks to a baseline creatinine of about 1.7 mg/dL after 12 months. Conclusion: In this case, a novel multimodal treatment strategy including daratumumab and imlifidase enabled successful kidney transplantation for a highly immunized patient with antiphospholipid antibodies.
伊立菲酶和达拉单抗成功为一名高度免疫、交叉配血阳性、血型不相容、患有系统性红斑狼疮和抗磷脂综合征的活体供体再移植受者脱敏
简介高度致敏患者的移植仍然是一大障碍。免疫患者如果不被优先考虑,等待移植的时间会更长;如果接受移植,移植结果也会更差。病例介绍:我们报告了一名患有系统性红斑狼疮(SLE)和抗磷脂综合征的 35 岁女性患者的 AB0 和 HLA 不相容活体肾移植手术。该患者的T细胞和B细胞补体依赖性细胞毒性(CDC)交叉配型呈阳性,且曾因肾静脉血栓形成而导致移植肾丢失。除了标准的免疫抑制外,我们还用静脉注射免疫球蛋白、利妥昔单抗、马抗胸腺细胞球蛋白、达拉单抗和伊立菲酶对患者进行治疗。所有 IgG 抗体对伊立菲酶治疗都很敏感。除供体特异性HLA抗体外,抗dsDNA抗体和抗磷脂抗体也被清除。患者最初出现移植功能延迟。两次肾活检(第7天和第14天)发现急性肾小管坏死,但没有HLA抗体介导的排斥迹象。移植后第 30 天,患者停止了血液透析,血肌酐水平在接下来的几周内下降到 12 个月后的 1.7 mg/dL 左右。结论在本病例中,包括达拉单抗和伊立菲酶在内的新型多模式治疗策略使一名高度免疫的抗磷脂抗体患者成功进行了肾移植。
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