Immune Problems in Central Nervous System Cell Therapy

被引:51
作者
Barker R.A. [1 ]
Widner H. [2 ]
机构
[1] Cambridge Center for Brain Repair, Department of Neurology, Cambridge
[2] Department of Clinical Neurosciences, Division of Neurology, Lund University Hospital
来源
NeuroRX | 2004年 / 1卷 / 4期
基金
英国医学研究理事会; 英国惠康基金;
关键词
brain; embryonic tissue; gene therapy; Immunity; transplantation; xenograft;
D O I
10.1602/neurorx.1.4.472
中图分类号
学科分类号
摘要
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. © 2004 The American Society for Experimental NeuroTherapeutics, Inc.
引用
收藏
页码:472 / 481
页数:9
相关论文
共 50 条
[41]   Immune Mediators of Pathology in Neurobrucellosis: From Blood to Central Nervous System [J].
Rodriguez, Ana M. ;
Victoria Delpino, M. ;
Cruz Miraglia, Maria ;
Giambartolomei, Guillermo H. .
NEUROSCIENCE, 2019, 410 :264-273
[42]   New insights into immune reconstitution inflammatory syndrome of the central nervous system [J].
Johnson, Tory P. ;
Nath, Avindra .
CURRENT OPINION IN HIV AND AIDS, 2014, 9 (06) :572-578
[43]   Gene therapy in autoimmune, demyelinating disease of the central nervous system [J].
Baker, D ;
Hankey, DJR .
GENE THERAPY, 2003, 10 (10) :844-853
[44]   Gene Therapy for Misfolding Protein Diseases of the Central Nervous System [J].
San Sebastian, Waldy ;
Samaranch, Lluis ;
Kells, Adrian P. ;
Forsayeth, John ;
Bankiewicz, Krystof S. .
NEUROTHERAPEUTICS, 2013, 10 (03) :498-510
[45]   Radiosurgery as Salvage Therapy for Primary Central Nervous System Lymphoma [J].
Chen, Clark C. ;
Hochberg, Fred ;
Batchelor, Tracy ;
Shih, Helen A. ;
Chakravarti, Arnab ;
Chapman, Paul ;
Loeffler, Jay .
RADIOSURGERY, VOL 7, 2010, 7 :276-287
[46]   Gene therapy in autoimmune, demyelinating disease of the central nervous system [J].
David Baker ;
D J R Hankey .
Gene Therapy, 2003, 10 :844-853
[47]   Gene Therapy for Misfolding Protein Diseases of the Central Nervous System [J].
Waldy San Sebastian ;
Lluis Samaranch ;
Adrian P. Kells ;
John Forsayeth ;
Krystof S. Bankiewicz .
Neurotherapeutics, 2013, 10 :498-510
[48]   Disulfidptosis: a new target for central nervous system disease therapy [J].
Chang, Jing ;
Liu, Danhong ;
Xiao, Yuqi ;
Tan, Boyao ;
Deng, Jun ;
Mei, Zhigang ;
Liao, Jun .
FRONTIERS IN NEUROSCIENCE, 2025, 19
[49]   Extracellular vesicle therapy for traumatic central nervous system disorders [J].
Zhang, Jing ;
Shi, Weipeng ;
Qu, Di ;
Yu, Tengbo ;
Qi, Chao ;
Fu, Haitao .
STEM CELL RESEARCH & THERAPY, 2022, 13 (01)
[50]   A review of gene therapy for the treatment of central nervous system tumors [J].
Qureshi, NH ;
Chiocca, EA .
CRITICAL REVIEWS IN ONCOGENESIS, 1999, 10 (04) :261-274