Department of Transfusion Medicine, NIH Clinical Center, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Experimental Transplantation and Immunotherapy Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Transfusion. 2021 Jun;61(6):1980-1986. doi: 10.1111/trf.16411. Epub 2021 Apr 26.
Donor-specific antibodies (DSA) to HLA have been associated with graft loss in hematopoietic progenitor cell (HPC) transplantation. Limited data associate therapeutic plasma exchange (TPE) with desensitization and successful engraftment. We report an attempt of desensitization and observed overshooting of DSA during transplantation.
A 27-year-old female with cutaneous T cell lymphoma was scheduled for HPC transplantation from her HLA-haploidentical half-sister, who carried the HLA-DRB113:03:01 allele. The patient had the corresponding DSA. Lacking an alternative donor option at the time, we attempted a desensitization approach by immunosuppression with tacrolimus and mycophenolate mofetil (MMF). Unexpectedly, DSA increased from a mean fluorescence intensity (MFI) of 1835 on day -63 to 9008 on day -7. The MFI increased further during 3 TPE procedures and intravenous immunoglobulin (IVIG) until day -1. After transplantation, the DSA remained elevated despite 2 more TPE/IVIG procedures and graft-versus-host disease prophylaxis with high-dose cyclophosphamide, sirolimus, and MMF. Flow cytometric crossmatch, initially negative, turned positive after transplantation. Primary graft failure occurred and was attributed to antibody-mediated rejection. A second transplantation from a 7/8 HLA-matched unrelated donor, not carrying DRB113:03 allele, resulted in successful engraftment.
Unexpected and rapid increases of a DSA can occur despite the use of current desensitization approaches. This is problematic when conditioning has already started, as such increases are unlikely to be overcome by TPE or other interventions for desensitization. Overshoot of DSA in HPC transplantation has rarely been reported. Its cause remains unclear and can include underlying disease, immunotherapy, chemotherapy, or TPE.
供者特异性抗体(DSA)与造血祖细胞(HPC)移植中的移植物丢失有关。有限的数据表明,治疗性血浆置换(TPE)与脱敏和成功植入有关。我们报告了一种脱敏尝试,并在移植过程中观察到 DSA 过度升高。
一名 27 岁女性患有皮肤 T 细胞淋巴瘤,计划接受其 HLA 半相合同父异母妹妹的 HPC 移植,妹妹携带 HLA-DRB113:03:01 等位基因。患者有相应的 DSA。当时缺乏替代供者选择,我们尝试通过使用他克莫司和吗替麦考酚酯(MMF)进行免疫抑制来进行脱敏。出乎意料的是,DSA 从 -63 天的平均荧光强度(MFI)1835 增加到 -7 天的 9008。在 3 次 TPE 和静脉注射免疫球蛋白(IVIG)过程中,MFI 进一步增加,直到 -1 天。移植后,尽管进行了 2 次 TPE/IVIG 以及高剂量环磷酰胺、西罗莫司和 MMF 预防移植物抗宿主病,但 DSA 仍持续升高。流式细胞交叉配型最初为阴性,移植后转为阳性。发生原发性移植物失败,归因于抗体介导的排斥反应。从 7/8 HLA 匹配的无关供体进行第二次移植,该供体不携带 DRB113:03 等位基因,导致成功植入。
尽管使用了当前的脱敏方法,但 DSA 的意外和快速增加仍可能发生。当已经开始预处理时,这种增加不太可能通过 TPE 或其他脱敏干预措施来克服,这是有问题的。HPC 移植中 DSA 过度升高很少有报道。其原因尚不清楚,可能包括潜在疾病、免疫治疗、化疗或 TPE。