2555: Belatacept in hand transplantation - Effectiveness and pitfalls
J. Grahammer, B. Zelger, B. Zelger, Annelies Muehlbacher, D. Oefner, S. Schneeberger, A. Weissenbacher
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引用次数: 0
Abstract
2555: Belatacept in hand transplantation Effectiveness and pitfalls Johanna Grahammer, MD, Bettina Zelger, MD, Bernhard Zelger, MD, Annelies Muehlbacher, MD, Dietmar Oefner, MD, Stefan Schneeberger, MD, and Annemarie Weissenbacher, MD Dept. of Visceral Transplant and Thoracic Surgery, Innsbruck Medical University, Innsbruck, Austria; Oxford Transplant Center, Oxford, UK Study purpose Belatacept (CTLA4Ig) is an emerging treatment in solid organ transplantation Effects on the development of donor specific antibodies (DSA) as well as its clinical safety in challenging immunological settings have yet to be explored. Methods Three hand transplanted patients have been converted to a Belatacept-based immunosuppressive regimen at 4 months, 6 y and 9 y after unilateral or bilateral hand and forearm transplantation Patients have received 5 mg/kg Belatacept every 2 weeks, the dosing interval was then extended to 4 weeks after 5 applications All 3 patients were kept on their baseline immunosuppressive medication, consisting of a CNI (Patients A, B, C) or mTOR inhibitor (Patients A and B) plus steroids (Patients A and B) and CellCept (Patient B). Results No adverse effects of Belatacept have been noted so far Patient C, who received Belatacept 4 months after transplantation, can successfully be kept on Tacrolimus monotherapy with a low trough level of »4–5 ng/ml This patient has never developed donorspecific antibodies, and displays normal histologic findings Patient A, who had previously developed DSA but was in a stable immunological state at the time of conversion, is now successfully tapered from baseline immunosuppression without evidence of rejection Patient B, who had DSA at the time of conversion, showed an increase of DSA and worsening graft appearance despite stable levels of his baseline immunosuppression, and needed escalation of his immunosuppression. Discussion The addition of Belatacept to an immunosuppressive regimen can be beneficial in hand transplantation However, our patients showed variable results depending on the immunological state at the time of conversion The application of Belatacept as a “œrescue” medication has to be discussed critically. CONTACT Johanna Grahammer, MD johanna.grahammer@tirol-kliniken.at © 2016 Johanna Grahammer, Bettina Zelger, Bernhard Zelger, Annelies Muehlbacher, Dietmar Oefner, Stefan Schneeberger, and Annemarie Weissenbacher. Published with license by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. VASCULARIZED COMPOSITE ALLOTRANSPLANTATION 2016, VOL. 3, NOS. 1–2, 27 http://dx.doi.org/10.1080/23723505.2016.1233009
2555: Belatacept在手部移植中的效果和缺陷
2555: Belatacept在手部移植中的有效性和缺陷Johanna Grahammer, MD, Bettina Zelger, MD, Bernhard Zelger, MD, Annelies Muehlbacher, MD, Dietmar Oefner, MD, Stefan Schneeberger, MD和Annemarie Weissenbacher, MD内脏移植和胸外科学系,因斯布鲁克医科大学,因斯布鲁克,奥地利;研究目的Belatacept (CTLA4Ig)是一种新兴的实体器官移植治疗药物,其对供体特异性抗体(DSA)产生的影响以及在具有挑战性的免疫环境下的临床安全性还有待探索。方法3例手部移植患者分别在单侧或双侧手部和前臂移植后4个月、6个月和9个月转换为基于Belatacept的免疫抑制方案。患者每2周接受5 mg/kg Belatacept, 5次应用后延长至4周。3例患者保持基线免疫抑制药物,包括CNI(患者a、B、C)或mTOR抑制剂(患者A和B)加类固醇(患者A和B)和CellCept(患者B)。结果迄今为止未发现Belatacept的不良反应,患者C在移植后4个月接受Belatacept治疗,可以成功地维持他克莫司单药治疗,低谷水平为»4 - 5 ng/ml。患者B在转换时患有DSA,尽管其基线免疫抑制水平稳定,但仍表现出DSA增加和移植物外观恶化,需要升级免疫抑制。在免疫抑制方案中加入Belatacept可能对手部移植有益,然而,我们的患者在转换时的免疫状态显示出不同的结果,Belatacept作为“œrescue”药物的应用必须进行严格的讨论。联系Johanna Grahammer, MD johanna.grahammer@tirol-kliniken.at©2016 Johanna Grahammer, Bettina Zelger, Bernhard Zelger, Annelies Muehlbacher, Dietmar Oefner, Stefan Schneeberger和Annemarie Weissenbacher。由Taylor & Francis授权出版。这是一篇在知识共享署名-非商业许可(http://creativecommons.org/licenses/by-nc/3.0/)条款下发布的开放获取文章,该许可允许在任何媒体上不受限制的非商业使用、分发和复制,前提是正确引用原始作品。指定作者的精神权利得到了维护。血管化复合异体移植,2016,VOL. 3, no .1 - 2,27 http://dx.doi.org/10.1080/23723505.2016.1233009
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