Achieving Tolerance in a Mismatched VCA Transplant While Reducing the Risk of GVHD: The Goal of Transient Chimerism

Bruce J. Swearingen, Jeff Chang, Tiffany Butts, S. Graves, R. Storb, D. Mathes
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Abstract

BACKGROUND: Transplantation of vascularized composite allografts (VCA) offers the opportunity to restore form and function. Clinical application is limited due to the necessity of life-long immunosuppression. One promising method of inducing tolerance to an organ allograft is the development of mixed chimerism. We have demonstrated that a nonmyeloablative stem cell transplant can lead to tolerance in a mismatched dog model. However, the application of this protocol has been limited by graft-versus-host disease (GVHD). We have observed several animals that, after an initial period of donor cell engraftment, lost their stem cell allograft but remained tolerant to the VCA. Conversely, animals that retained persistent donor cell chimerism inevitably developed GVHD. The hypothesis for this study was that our non-myeloablative hematopoietic stem cell transplant protocol could be used to induce tolerance to a recipient VCA without the need for persistent donor cell chimerism.
在降低GVHD风险的同时实现错配VCA移植的耐受性:短暂嵌合的目标
背景:血管化复合同种异体移植(VCA)提供了恢复形态和功能的机会。由于需要终身免疫抑制,临床应用受到限制。一种很有前途的诱导对同种异体器官移植耐受的方法是发展混合嵌合。我们已经证明,非清髓性干细胞移植可以在不匹配的狗模型中导致耐受性。然而,该方案的应用受到移植物抗宿主病(GVHD)的限制。我们已经观察到一些动物,在供体细胞移植的初始阶段,失去了他们的干细胞移植物,但仍然对VCA耐受。相反,保留持续供体细胞嵌合的动物不可避免地发展为GVHD。本研究的假设是,我们的非清髓性造血干细胞移植方案可用于诱导对受体VCA的耐受性,而无需持续的供体细胞嵌合。
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