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通过给予受体来源的未成熟树突状细胞和次优免疫抑制实现供体特异性同种异体移植耐受。

Donor-specific allograft tolerance by administration of recipient-derived immature dendritic cells and suboptimal immunosuppression.

作者信息

Bériou Gaëlle, Pêche Hélène, Guillonneau Carole, Merieau Emmanuel, Cuturi Maria-Cristina

机构信息

Institut National de la Santé et de la Recherche Médicale Unité 643, 44093 Nantes Cedex 1, France.

出版信息

Transplantation. 2005 Apr 27;79(8):969-72. doi: 10.1097/01.tp.0000158277.50073.35.

Abstract

We recently showed that injection of recipient-type immature bone marrow-derived dendritic cells (iBMDCs) the day before transplantation induced a significant prolongation of allograft survival. This study aimed at improving the administration protocol to induce allograft tolerance. Various amounts of iBMDCs were administered to syngeneic LEW.1A rats before and after transplantation of an allogeneic LEW.1W heart, with or without additional suboptimal immunosuppression. Allograft survival was not improved by repeated injections of syngeneic iBMDCs or by additional treatment with low-dose rapamycin. Combining injections of iBMDCs and LF 15-0195 showed a striking synergistic effect and induced definitive allograft acceptance in 92% of recipients. Tolerant recipients accepted donor-type, but not third-party type skin grafts, suggesting the development of regulatory mechanisms capable of maintaining donor-specific tolerance. The reported findings may contribute to the development of new therapeutic strategies to induce transplantation tolerance in humans.

摘要

我们最近发现,在移植前一天注射受体型未成熟骨髓来源的树突状细胞(iBMDCs)可显著延长同种异体移植物的存活时间。本研究旨在改进给药方案以诱导同种异体移植物耐受。在同种异体LEW.1W心脏移植前后,向同基因LEW.1A大鼠给予不同剂量的iBMDCs,同时给予或不给予额外的次优免疫抑制。重复注射同基因iBMDCs或低剂量雷帕霉素的额外治疗均未改善同种异体移植物的存活。联合注射iBMDCs和LF 15-0195显示出显著的协同效应,并在92%的受体中诱导了明确的同种异体移植物接受。耐受的受体接受供体型皮肤移植,但不接受第三方型皮肤移植,这表明能够维持供体特异性耐受的调节机制的发展。所报道的研究结果可能有助于开发新的治疗策略以诱导人类移植耐受。

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