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本文引用的文献

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Intracerebral cytokine profiles in adult rats grafted with neural tissue of different immunological disparity.
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2
Complement regulatory proteins are expressed at low levels in embryonic human, wild type and transgenic porcine neural tissue.补体调节蛋白在人类胚胎、野生型和转基因猪神经组织中低水平表达。
Xenotransplantation. 2004 Jan;11(1):60-71. doi: 10.1111/j.1399-3089.2004.00084.x.
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Studies on the problem of corneal homografts.角膜同种移植问题的研究。
Proc R Soc Lond B Biol Sci. 1953 Jul 15;141(904):392-406. doi: 10.1098/rspb.1953.0049.
4
A double-blind controlled trial of bilateral fetal nigral transplantation in Parkinson's disease.帕金森病双侧胎儿黑质移植的双盲对照试验。
Ann Neurol. 2003 Sep;54(3):403-14. doi: 10.1002/ana.10720.
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Induction of operational tolerance to discordant dopaminergic porcine xenografts.诱导对不匹配的多巴胺能猪异种移植物的操作耐受性。
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Immune parameters relevant to neural xenograft survival in the primate brain.
Xenotransplantation. 2003 Jan;10(1):41-9. doi: 10.1034/j.1399-3089.2003.01130.x.
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Subretinal transplantation of brain-derived precursor cells to young RCS rats promotes photoreceptor cell survival.
Exp Eye Res. 2002 Jul;75(1):23-37. doi: 10.1006/exer.2001.1172.
8
Fetal neural grafts for Huntington's disease: a prospective view.
Mov Disord. 2002 May;17(3):439-44. doi: 10.1002/mds.10117.
9
Generation of histocompatible tissues using nuclear transplantation.利用核移植技术生成组织相容性组织。
Nat Biotechnol. 2002 Jul;20(7):689-96. doi: 10.1038/nbt703. Epub 2002 Jun 3.
10
The potential for circuit reconstruction by expanded neural precursor cells explored through porcine xenografts in a rat model of Parkinson's disease.通过猪异种移植在帕金森病大鼠模型中探索扩增神经前体细胞进行神经回路重建的潜力。
Exp Neurol. 2002 May;175(1):98-111. doi: 10.1006/exnr.2002.7889.

中枢神经系统细胞治疗中的免疫问题。

Immune problems in central nervous system cell therapy.

作者信息

Barker Roger A, Widner Håkan

机构信息

Cambridge Center for Brain Repair and Department of Neurology, Cambridge CB2 6SP, United Kingdom.

出版信息

NeuroRx. 2004 Oct;1(4):472-81. doi: 10.1602/neurorx.1.4.472.

DOI:10.1602/neurorx.1.4.472
PMID:15717048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC534953/
Abstract

Transplantation of cells and tissues to the mammalian brain and CNS has revived the interest in the immunological status of brain and its response to grafted tissue. The previously held view that the brain was an absolute "immunologically privileged site" allowing indefinite survival without rejection of grafts of cells has proven to be wrong. Thus, the brain should be regarded as a site where immune responses can occur, albeit in a modified form, and under certain circumstances these are as vigorous as those seen in other peripheral sites. Clinical cell transplant trials have now been performed in Parkinson's disease, Huntington's disease, demyelinating diseases, retinal disorders, stroke, epilepsy, and even deafness, and normally are designed as cell replacement strategies, although implantation of genetically modified cells for supplementation of growth factors has also been tried. In addition, some disorders of the CNS for which cell therapies are being considered have an immunological basis, such as multiple sclerosis, which further complicates the situation. Embryonic neural tissue allografted into the CNS of animals and patients with neurodegenerative conditions survives, makes and receives synapses, and ameliorates behavioral deficits. The use of aborted human tissue is logistically and ethically complicated, which has lead to the search for alternative sources of cells, including xenogeneic tissue, genetically modified cells, and stem cells, all of which can and will induce some level of immune reaction. We review some of the immunological factors involved in transplantation of cells to CNS.

摘要

将细胞和组织移植到哺乳动物的脑和中枢神经系统,重新唤起了人们对脑的免疫状态及其对移植组织反应的兴趣。先前认为脑是绝对的“免疫特惠部位”,能使移植的细胞无限期存活而不被排斥的观点已被证明是错误的。因此,脑应被视为一个能发生免疫反应的部位,尽管其形式有所改变,而且在某些情况下,这些反应与在其他外周部位所见的反应一样强烈。目前已在帕金森病、亨廷顿病、脱髓鞘疾病、视网膜疾病、中风、癫痫甚至耳聋患者中开展了临床细胞移植试验,这些试验通常被设计为细胞替代策略,不过也有人尝试植入经过基因改造的细胞以补充生长因子。此外,一些正在考虑采用细胞疗法的中枢神经系统疾病具有免疫学基础,比如多发性硬化症,这使得情况更加复杂。移植到患有神经退行性疾病的动物和患者中枢神经系统中的胚胎神经组织能够存活、形成并接收突触,还能改善行为缺陷。使用流产的人体组织在后勤和伦理方面都很复杂,这促使人们寻找细胞的替代来源,包括异种组织、基因改造细胞和干细胞,所有这些都可能并将会引发一定程度的免疫反应。我们将综述细胞移植到中枢神经系统过程中涉及的一些免疫因素。