Orandi Babak J, Zachary Andrea A, Dagher Nabil N, Bagnasco Serena M, Garonzik-Wang Jacqueline M, Van Arendonk Kyle J, Gupta Natasha, Lonze Bonnie E, Alachkar Nada, Kraus Edward S, Desai Niraj M, Locke Jayme E, Racusen Lorraine C, Segev Dorry L, Montgomery Robert A
1 Department of Surgery, Johns Hopkins Medical Institutions, Baltimore, MD. 2 Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD. 3 Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD. 4 Department of Surgery, University of Alabama, Birmingham, AL. 5 Address correspondence to: Robert Montgomery, M.D., DPhil, 720 Rutland Avenue, Ross 765, Baltimore, MD 21205.
Transplantation. 2014 Oct 27;98(8):857-63. doi: 10.1097/TP.0000000000000298.
Incompatible live donor kidney transplantation is associated with an increased rate of antibody-mediated rejection (AMR) and subsequent transplant glomerulopathy. For patients with severe, oliguric AMR, graft loss is inevitable without timely intervention.
We reviewed our experience rescuing kidney allografts with this severe AMR phenotype by using splenectomy alone (n=14), eculizumab alone (n=5), or splenectomy plus eculizumab (n=5), in addition to plasmapheresis.
The study population was 267 consecutive patients with donor-specific antibody undergoing desensitization. In the first 3 weeks after transplantation (median=6 days), 24 patients developed sudden onset oliguria and rapidly rising serum creatinine with marked rebound of donor-specific antibody, and a biopsy that showed features of AMR. At a median follow-up of 533 days, 4 of 14 splenectomy-alone patients experienced graft loss (median=320 days), compared to four of five eculizumab-alone patients with graft failure (median=95 days). No patients treated with splenectomy plus eculizumab experienced graft loss. There was more chronic glomerulopathy in the splenectomy-alone and eculizumab-alone groups at 1 year, whereas splenectomy plus eculizumab patients had almost no transplant glomerulopathy.
These data suggest that for patients manifesting early severe AMR, splenectomy plus eculizumab may provide an effective intervention for rescuing and preserving allograft function.
不兼容的活体供肾移植与抗体介导的排斥反应(AMR)发生率增加及随后的移植肾小球病相关。对于严重少尿型AMR患者,若不及时干预,移植肾丢失不可避免。
我们回顾了单独使用脾切除术(n = 14)、单独使用依库珠单抗(n = 5)或脾切除术加依库珠单抗(n = 5)联合血浆置换抢救具有这种严重AMR表型的同种异体移植肾的经验。
研究人群为267例连续接受脱敏治疗的供体特异性抗体患者。移植后的前3周(中位数 = 6天),24例患者出现突发少尿,血清肌酐迅速升高,供体特异性抗体明显反弹,活检显示有AMR特征。中位随访533天,14例单独接受脾切除术的患者中有4例移植肾丢失(中位数 = 320天),而5例单独使用依库珠单抗的患者中有4例移植失败(中位数 = 95天)。接受脾切除术加依库珠单抗治疗的患者无一例移植肾丢失。单独脾切除术组和单独依库珠单抗组在1年时慢性肾小球病更多,而脾切除术加依库珠单抗组几乎没有移植肾小球病。
这些数据表明,对于早期出现严重AMR的患者,脾切除术加依库珠单抗可能为抢救和保留同种异体移植肾功能提供有效的干预措施。