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从携带心脏同种异体移植物的耐受小鼠中获得的供体特异性调节性T细胞可促进混合嵌合体形成并延长肠道同种异体移植物存活时间。

Donor-Specific Regulatory T Cells Acquired from Tolerant Mice Bearing Cardiac Allograft Promote Mixed Chimerism and Prolong Intestinal Allograft Survival.

作者信息

Shen Xiao-Fei, Jiang Jin-Peng, Yang Jian-Jun, Wang Wei-Zhong, Guan Wen-Xian, Du Jun-Feng

机构信息

Department of General Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School , Nanjing , China.

Department of Rehabilitation Medicine, PLA Army General Hospital , Beijing , China.

出版信息

Front Immunol. 2016 Nov 17;7:511. doi: 10.3389/fimmu.2016.00511. eCollection 2016.

DOI:10.3389/fimmu.2016.00511
PMID:27909438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5113131/
Abstract

The induction of donor-specific transplant tolerance has always been a central problem for small bowel transplantation (SBT), which is thought to be the best therapy for end-stage bowel failure. With the development of new tolerance-inducing strategies, mixed chimerism induced by co-stimulation blockade has become most potent for tolerance of allografts, such as skin, kidney, and heart. However, a lack of clinically available co-stimulation blockers has hindered efficient application in humans. Furthermore, unlike those for other types of solid organ transplantation, strategies to induce robust mixed chimerism for intestinal allografts have not been fully developed. To improve current mixed chimerism induction protocols for future clinical application, we developed a new protocol using donor-specific regulatory T (Treg) cells from mice with heart allograft tolerance, immunosuppressive drugs which could be used clinically and low doses of irradiation. Our results demonstrated that donor-specific Treg cells acquired from tolerant mice after expansion generate stable chimerism and lead to acceptance of intestinal allograft. Increased intragraft Treg cells and clonal deletion contribute to the development of SBT tolerance.

摘要

诱导供体特异性移植耐受一直是小肠移植(SBT)的核心问题,小肠移植被认为是终末期肠衰竭的最佳治疗方法。随着新型耐受诱导策略的发展,共刺激阻断诱导的混合嵌合体已成为对皮肤、肾脏和心脏等同种异体移植物产生耐受的最有效方法。然而,缺乏临床可用的共刺激阻断剂阻碍了其在人类中的有效应用。此外,与其他类型的实体器官移植不同,诱导肠道同种异体移植物产生强大混合嵌合体的策略尚未得到充分发展。为了改进当前的混合嵌合体诱导方案以便未来临床应用,我们开发了一种新方案,使用来自具有心脏同种异体移植耐受性的小鼠的供体特异性调节性T(Treg)细胞、可临床使用的免疫抑制药物和低剂量辐射。我们的结果表明,从耐受小鼠中获取并扩增后的供体特异性Treg细胞可产生稳定的嵌合体,并导致肠道同种异体移植被接受。移植内Treg细胞增加和克隆清除有助于小肠移植耐受的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/cc1d3c02efec/fimmu-07-00511-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/c7b5bb6051f9/fimmu-07-00511-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/d59399aa3b08/fimmu-07-00511-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/784fb3c193a6/fimmu-07-00511-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/c598be1d74a7/fimmu-07-00511-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/cc1d3c02efec/fimmu-07-00511-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/c7b5bb6051f9/fimmu-07-00511-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/d59399aa3b08/fimmu-07-00511-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/784fb3c193a6/fimmu-07-00511-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/c598be1d74a7/fimmu-07-00511-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/5113131/cc1d3c02efec/fimmu-07-00511-g005.jpg

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本文引用的文献

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IL-2/α-IL-2 Complex Treatment Cannot Be Substituted for the Adoptive Transfer of Regulatory T cells to Promote Bone Marrow Engraftment.白细胞介素-2/α-白细胞介素-2复合物治疗不能替代调节性T细胞的过继转移来促进骨髓植入。
PLoS One. 2016 Jan 5;11(1):e0146245. doi: 10.1371/journal.pone.0146245. eCollection 2016.
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Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine.
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Immunity. 2015 Oct 20;43(4):817-29. doi: 10.1016/j.immuni.2015.09.007.
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Requirement of full TCR repertoire for regulatory T cells to maintain intestinal homeostasis.调节性T细胞维持肠道稳态对完整T细胞受体库的需求。
Proc Natl Acad Sci U S A. 2015 Oct 13;112(41):12770-5. doi: 10.1073/pnas.1516617112. Epub 2015 Sep 29.
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Deletional and regulatory mechanisms coalesce to drive transplantation tolerance through mixed chimerism.缺失性和调节性机制通过混合嵌合体共同作用来驱动移植耐受。
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IDO expressing dendritic cells suppress allograft rejection of small bowel transplantation in mice by expansion of Foxp3+ regulatory T cells.表达吲哚胺2,3-双加氧酶的树突状细胞通过扩增Foxp3+调节性T细胞抑制小鼠小肠移植的同种异体排斥反应。
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