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本文引用的文献

1
Pillars Article: Control of Regulatory T Cell Development by the Transcription Factor Foxp3. Science 2003. 299: 1057-1061.支柱文章:转录因子Foxp3对调节性T细胞发育的控制。《科学》2003年。299卷:1057 - 1061页。
J Immunol. 2017 Feb 1;198(3):981-985.
2
Induction of Foxp3-expressing regulatory T-cells by donor blood transfusion is required for tolerance to rat liver allografts.供者输血诱导 Foxp3 表达的调节性 T 细胞是大鼠肝移植耐受所必需的。
PLoS One. 2009 Nov 23;4(11):e7840. doi: 10.1371/journal.pone.0007840.
3
Linked suppression across an MHC-mismatched barrier in a miniature swine kidney transplantation model.小型猪肾移植模型中跨越主要组织相容性复合体不匹配屏障的连锁抑制
J Immunol. 2008 Sep 15;181(6):4027-36. doi: 10.4049/jimmunol.181.6.4027.
4
Role of the thymus in transplantation tolerance in miniature swine: V. Deficiency of the graft-to-thymus pathway of tolerance induction in recipients of cardiac transplants.胸腺在小型猪移植耐受中的作用:V. 心脏移植受者中耐受诱导的移植物至胸腺途径缺陷。
Transplantation. 2006 Feb 27;81(4):607-13. doi: 10.1097/01.tp.0000198735.17555.f1.
5
Long-term acceptance of fully allogeneic cardiac grafts by cotransplantation of vascularized thymus in miniature swine.通过在小型猪中共同移植血管化胸腺实现完全异体心脏移植物的长期存活
Transplantation. 2006 Jan 15;81(1):26-35. doi: 10.1097/01.tp.0000200368.03991.e0.
6
Recruitment of Foxp3+ T regulatory cells mediating allograft tolerance depends on the CCR4 chemokine receptor.介导同种异体移植耐受的Foxp3+调节性T细胞的募集依赖于CCR4趋化因子受体。
J Exp Med. 2005 Apr 4;201(7):1037-44. doi: 10.1084/jem.20041709.
7
Induction of foxP3+ regulatory T cells in the periphery of T cell receptor transgenic mice tolerized to transplants.在对移植产生耐受的T细胞受体转基因小鼠外周诱导产生FoxP3+调节性T细胞。
J Immunol. 2004 May 15;172(10):6003-10. doi: 10.4049/jimmunol.172.10.6003.
8
Role of the thymus in transplantation tolerance in miniature Swine: IV. The thymus is required during the induction phase, but not the maintenance phase, of renal allograft tolerance.胸腺在小型猪移植耐受中的作用:IV. 肾移植耐受的诱导期需要胸腺,但维持期不需要。
Transplantation. 2004 Apr 15;77(7):979-85. doi: 10.1097/01.tp.0000116416.10799.c6.
9
Vascularized thymic lobe transplantation in miniature swine: thymopoiesis and tolerance induction across fully MHC-mismatched barriers.小型猪血管化胸腺叶移植:跨越完全MHC不匹配屏障的胸腺生成和耐受性诱导。
Proc Natl Acad Sci U S A. 2004 Mar 16;101(11):3827-32. doi: 10.1073/pnas.0306666101. Epub 2004 Mar 8.
10
Pretransplant blood transfusion without additional immunotherapy generates CD25+CD4+ regulatory T cells: a potential explanation for the blood-transfusion effect.无额外免疫疗法的移植前输血可产生CD25 + CD4 + 调节性T细胞:对输血效应的一种潜在解释。
Transplantation. 2003 Aug 15;76(3):449-55. doi: 10.1097/01.TP.0000083043.84630.99.

小型猪通过过继转移诱导肾移植耐受。

The induction of tolerance of renal allografts by adoptive transfer in miniature swine.

机构信息

Transplantation Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Am J Transplant. 2013 May;13(5):1193-202. doi: 10.1111/ajt.12194. Epub 2013 Mar 6.

DOI:10.1111/ajt.12194
PMID:23464595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3671754/
Abstract

Our previous in vitro data have demonstrated that regulatory mechanisms are involved in tolerance of class I-mismatched renal allografts in miniature swine treated with 12 days of high dose Cyclsporin A. In this study, we attempted to induce tolerance of class I-mismatched kidneys by adoptive transfer of cells and/or kidneys from long-term tolerant animals. Fifteen SLA(dd) miniature swine received 1.5 Gy whole body irradiation and class I-mismatched (SLA(gg) ) kidneys from naïve pigs with or without cotransplanted kidneys and/or adoptively transferred cells from long-term tolerant (LTT) SLA(dd) recipients of SLA(gg) grafts. In addition, three SLA(dd) miniature swine received class I mismatched kidney with adoptively transferred cells from LTT SLA(dd) recipients. Naïve kidneys transplanted without a LTT kidney were rejected within 9 days. All recipients of naive kidneys along with cells and kidney grafts from LTT animals showed markedly prolonged survival of the naive renal grafts (day 28, >150 and >150 days). These studies suggest that (1) tolerated kidneys have potent regulatory effects and (2) cells from LTT animals infused in conjunction with kidney grafts augment these regulatory effects. To our knowledge, these studies represent the first demonstration of successful adoptive transfer of tolerance in large animals.

摘要

我们之前的体外数据表明,在接受 12 天高剂量环孢素 A 治疗的小型猪中,调节机制参与了对 I 类错配肾移植的耐受。在这项研究中,我们试图通过从长期耐受动物中过继转移细胞和/或肾脏来诱导 I 类错配肾脏的耐受。15 只 SLA(dd)小型猪接受 1.5 Gy 全身照射,并接受来自幼稚猪的 I 类错配(SLA(gg))肾脏,或同时接受来自长期耐受(LTT)SLA(dd)接受者的 SLA(gg)移植物的共移植肾脏和/或过继转移细胞。此外,3 只 SLA(dd)小型猪接受了来自 LTT SLA(dd)接受者的过继转移细胞的 I 类错配肾脏。没有 LTT 肾脏的幼稚肾脏移植在 9 天内被排斥。所有接受幼稚肾脏以及来自 LTT 动物的细胞和肾脏移植物的受者均表现出幼稚肾移植物的存活明显延长(第 28 天,>150 天和>150 天)。这些研究表明:(1)耐受的肾脏具有强大的调节作用;(2)来自 LTT 动物的细胞与肾脏移植物一起输注可增强这些调节作用。据我们所知,这些研究代表了在大型动物中成功进行过继转移耐受的首次证明。