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.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING
Kaitlyn Dykes, Dimitrios Tzachanis, Divya Koura
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引用次数: 0

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.

同种异体造血干细胞移植后钙神经蛋白抑制剂神经毒性的疑难病例与成功的新解决方案:细胞毒性 T 淋巴细胞相关蛋白 4-免疫球蛋白阻滞剂用于预防 GVHD。
异基因造血细胞移植(HCT)后的免疫抑制方案是作为移植物抗宿主病(GVHD)的预防措施。大多数 GVHD 预防方案都以钙神经蛋白抑制剂(CNIs)为基础。遗憾的是,钙神经蛋白抑制剂的相关发病率很高,常常不能耐受,而且经常需要停药。对于在必须永久停用 CNIs 的情况下应使用哪种替代免疫抑制剂,目前尚未达成共识。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,已被广泛用于自身免疫性疾病患者和移植后免疫抑制。目前有两种 CTLA4-Ig 制剂:贝拉他赛普和阿巴他赛普。贝拉他赛普被常规用于成人肾移植以预防排斥反应,阿巴他赛普已被美国食品药品管理局(FDA)批准用于接受匹配或一个等位基因不匹配的非亲属异基因造血干细胞移植患者的GVHD预防。在本文中,我们描述了一个病例:在接受单倍体同种异基因造血干细胞移植的神经毒性患者中,阿帕他赛在标签外替代他克莫司用于 GVHD 预防。该病例表明,在需要停用 CNI 的病例中,CTLA4-Ig 阻断可能是 CNI 的良好替代品,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
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