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2
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本文引用的文献

1
Transforming growth factor β1 and Fas ligand synergistically enhance immune tolerance in dendritic cells in liver transplantation.转化生长因子β1与Fas配体协同增强肝移植中树突状细胞的免疫耐受。
J Surg Res. 2017 Oct;218:180-193. doi: 10.1016/j.jss.2017.05.040. Epub 2017 Jun 16.
2
Replenishing Regulatory T Cells to Halt Depigmentation in Vitiligo.补充调节性T细胞以阻止白癜风的色素脱失
J Investig Dermatol Symp Proc. 2017 Oct;18(2):S38-S45. doi: 10.1016/j.jisp.2016.10.023.
3
Peripheral blood Th9 cells reconstitution and its relationship with acute graft-versus-host disease after matched-sibling peripheral blood hematopoietic stem cell transplantation.同胞全相合外周血造血干细胞移植后外周血Th9细胞重建及其与急性移植物抗宿主病的关系
Am J Transl Res. 2017 Aug 15;9(8):3623-3632. eCollection 2017.
4
Stabilizing human regulatory T cells for tolerance inducing immunotherapy.稳定人类调节性T细胞以进行诱导耐受的免疫治疗。
Immunotherapy. 2017 Aug;9(9):735-751. doi: 10.2217/imt-2017-0017. Epub 2017 Aug 3.
5
Harnessing the properties of dendritic cells in the pursuit of immunological tolerance.利用树突状细胞的特性来寻求免疫耐受。
Biomed J. 2017 Apr;40(2):80-93. doi: 10.1016/j.bj.2017.01.002. Epub 2017 Apr 26.
6
The Importance of Dendritic Cells in Maintaining Immune Tolerance.树突状细胞在维持免疫耐受中的重要性。
J Immunol. 2017 Mar 15;198(6):2223-2231. doi: 10.4049/jimmunol.1601629.
7
Marked in Vivo Donor Regulatory T Cell Expansion via Interleukin-2 and TL1A-Ig Stimulation Ameliorates Graft-versus-Host Disease but Preserves Graft-versus-Leukemia in Recipients after Hematopoietic Stem Cell Transplantation.通过白细胞介素-2和TL1A-Ig刺激在体内显著扩增供体调节性T细胞可改善造血干细胞移植受者的移植物抗宿主病,但保留移植物抗白血病效应。
Biol Blood Marrow Transplant. 2017 May;23(5):757-766. doi: 10.1016/j.bbmt.2017.02.013. Epub 2017 Feb 20.
8
Stem Cell Therapy for Neonatal Disorders: Prospects and Challenges.新生儿疾病的干细胞治疗:前景与挑战
Yonsei Med J. 2017 Mar;58(2):266-271. doi: 10.3349/ymj.2017.58.2.266.
9
An essential role for the IL-2 receptor in T cell function.白细胞介素-2受体在T细胞功能中起重要作用。
Nat Immunol. 2016 Nov;17(11):1322-1333. doi: 10.1038/ni.3540. Epub 2016 Sep 5.
10
Mixed lymphocyte reaction induced by multiple alloantigens and the role for IL-10 in proliferation inhibition.由多种同种异体抗原诱导的混合淋巴细胞反应及 IL-10 在增殖抑制中的作用。
Burns Trauma. 2014 Jan 26;2(1):24-8. doi: 10.4103/2321-3868.126088. eCollection 2014.

[早产儿同种异体细胞移植免疫耐受的研究进展]

[Research advances in immune tolerance of allogeneic cell transplantation in preterm infants].

作者信息

Lyu Can, Qu Yi, Mu De-Zhi

机构信息

Department of Pediatrics, West China Second University Hospital/Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu 610041, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2018 Apr;20(4):338-340. doi: 10.7499/j.issn.1008-8830.2018.04.016.

DOI:10.7499/j.issn.1008-8830.2018.04.016
PMID:29658462
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7390031/
Abstract

Preterm infants are a special group, and related severe neurological, respiratory, and digestive disorders have high disability/fatality rates. Allogeneic cell transplantation may be an effective method for the prevention and treatment of these diseases. At present, animal studies have been conducted for allogeneic cell transplantation in the treatment of hypoxic-ischemic encephalopathy, bronchopulmonary dysplasia, and necrotizing enterocolitis. The main difficulty of this technique is graft-versus-host reaction (GVHR), and successful induction of immune tolerance needs to be achieved in order to solve this problem. This article reviews the research advances in immune tolerance of allogeneic cell transplantation in preterm infants.

摘要

早产儿是一个特殊群体,与之相关的严重神经、呼吸和消化系统疾病具有较高的致残率/死亡率。异基因细胞移植可能是预防和治疗这些疾病的有效方法。目前,已经开展了异基因细胞移植治疗缺氧缺血性脑病、支气管肺发育不良和坏死性小肠结肠炎的动物研究。这项技术的主要难点是移植物抗宿主反应(GVHR),需要成功诱导免疫耐受以解决这一问题。本文综述了早产儿异基因细胞移植免疫耐受的研究进展。