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钙调磷酸酶抑制剂同种异体造血干细胞移植后神经毒性的疑难病例:细胞毒性 T 淋巴细胞相关蛋白 4-免疫球蛋白阻断用于移植物抗宿主病预防的成功新方案。

A Difficult Case of Calcineurin Inhibitor Neurotoxicity Post-Haploidentical HCT With a Successful Novel Solution: Cytotoxic T-Lymphocyte-Associated Protein 4-Immunoglobulin Blockade for GVHD Prophylaxis.

机构信息

Division of Hematology Oncology, Moores Cancer Center, University of California San Diego, La Jolla, CA, USA.

Division of Blood & Bone Marrow Transplantation, Moores Cancer Center, University of California San Diego, La Jolla, CA, USA.

出版信息

Cell Transplant. 2024 Jan-Dec;33:9636897241265249. doi: 10.1177/09636897241265249.

Abstract

Post-allogeneic hematopoietic cell transplant (HCT) immunosuppression regimens are given as graft-versus-host disease (GVHD) prophylaxis. Most GVHD prophylaxis regimens are based on calcineurin inhibitors (CNIs). Unfortunately, CNIs are associated with significant associated morbidity, frequently cannot be tolerated, and often need to be discontinued. There is no consensus as to which alternative immunosuppression should be used in cases where CNIs have to be permanently discontinued. Cytotoxic T-lymphocyte-associated protein 4-immunoglobulin (CTLA4-Ig) blocking agents are well tolerated and have been used extensively in patients with autoimmune disease and as post-transplant immunosuppression. There are two CTLA4-Ig agents: belatacept and abatacept. Belatacept is routinely used in adult kidney transplantation to prevent rejection and abatacept has been approved by the Food and Drug Administration (FDA) for GVHD prophylaxis in patients undergoing a matched or one allele-mismatched unrelated allogenic HCT. Herein, we describe a case in which abatacept was given off-label to replace tacrolimus GVHD prophylaxis in a patient with neurotoxicity undergoing haploidentical HCT. This case suggests that CTLA4-Ig blockade may be a good alternative to a CNI in cases where the CNI needs to be discontinued and warrants further investigation.

摘要

在异基因造血细胞移植(HCT)后,会给予免疫抑制方案作为移植物抗宿主病(GVHD)的预防措施。大多数 GVHD 预防方案基于钙调磷酸酶抑制剂(CNI)。不幸的是,CNI 会引起明显的相关疾病,通常无法耐受,并且经常需要停药。在需要永久性停用 CNI 的情况下,应使用哪种替代免疫抑制剂尚无共识。细胞毒性 T 淋巴细胞相关蛋白 4-免疫球蛋白(CTLA4-Ig)阻断剂具有良好的耐受性,并已广泛用于自身免疫性疾病患者和移植后的免疫抑制治疗。目前有两种 CTLA4-Ig 制剂:贝利尤单抗和阿巴西普。贝利尤单抗常规用于成人肾移植以预防排斥反应,而阿巴西普已获得美国食品和药物管理局(FDA)批准,可用于接受匹配或一个等位基因错配的无关异体 HCT 的患者的 GVHD 预防。在此,我们描述了 1 例因神经毒性而行单倍体相合 HCT 的患者,阿巴西普被超说明书使用来替代他克莫司进行 GVHD 预防的案例。该案例提示,在需要停用 CNI 的情况下,CTLA4-Ig 阻断可能是 CNI 的良好替代方案,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2589/11289812/23010f7f0d20/10.1177_09636897241265249-fig1.jpg

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