Immune responses to adenovirus vectors in the nervous system

被引:137
作者
Wood, MJA [1 ]
Charlton, HM [1 ]
Wood, KJ [1 ]
Kajiwara, K [1 ]
Byrnes, AP [1 ]
机构
[1] JOHN RADCLIFFE HOSP,NUFFIELD DEPT SURG,OXFORD OX3 9DU,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/S0166-2236(96)10060-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Non-replicating adenovirus vectors are being developed as vehicles for gene transfer into cells of the nervous system. An important requirement for successful gene transfer is the absence of deleterious cytotoxic or inflammatory side effects of the delivery system. Despite offering relatively stable reporter gene expression, currently available adenovirus vectors also elicit immune responses in the brain, both at the site of vector delivery and at synaptically linked distant sites, However, although an anti-viral T-lymphocyte response eliminates the vector and damages local tissue in many peripheral organs, the immune response to adenovirus in the brain is less effective and enables the vector to persist. Nevertheless, in this persistent state the adenovirus vector remains a potential target for a destructive immune response that can also cause local demyelination. The development of strategies to minimize this damaging immune response, through either vector modification or immunomodulation, will be crucial for the future success of genetic therapies in the brain.
引用
收藏
页码:497 / 501
页数:5
相关论文
共 47 条
[11]   GENE-THERAPY FOR NEUROLOGICAL DISORDERS [J].
FRIEDMANN, T .
TRENDS IN GENETICS, 1994, 10 (06) :210-214
[12]   A MOUSE MODEL FOR INVESTIGATING THE MOLECULAR PATHOGENESIS OF ADENOVIRUS PNEUMONIA [J].
GINSBERG, HS ;
MOLDAWER, LL ;
SEHGAL, PB ;
REDINGTON, M ;
KILIAN, PL ;
CHANOCK, RM ;
PRINCE, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1651-1655
[13]  
GLORIOSO JC, 1992, SEMIN VIROL, V3, P265
[14]   LYMPHOCYTE-T ENTRY INTO THE CENTRAL-NERVOUS-SYSTEM [J].
HICKEY, WF ;
HSU, BL ;
KIMURA, H .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 28 (02) :254-260
[15]   NEURONAL CELLS ARE DEFICIENT IN LOADING PEPTIDES ONTO MHC CLASS-I MOLECULES [J].
JOLY, E ;
OLDSTONE, MBA .
NEURON, 1992, 8 (06) :1185-1190
[16]   LONG-TERM GENE-EXPRESSION AND PHENOTYPIC CORRECTION USING ADENOASSOCIATED VIRUS VECTORS IN THE MAMMALIAN BRAIN [J].
KAPLITT, MG ;
LEONE, P ;
SAMULSKI, RJ ;
XIAO, X ;
PFAFF, DW ;
OMALLEY, KL ;
DURING, MJ .
NATURE GENETICS, 1994, 8 (02) :148-154
[17]  
Karpati G, 1996, TRENDS NEUROSCI, V19, P49
[18]  
KASSEISLER A, 1994, GENE THER, V1, P395
[19]   LONG-TERM HEPATIC ADENOVIRUS-MEDIATED GENE-EXPRESSION IN MICE FOLLOWING CTLA4LG ADMINISTRATION [J].
KAY, MA ;
HOLTERMAN, AX ;
MEUSE, L ;
GOWN, A ;
OCHS, HD ;
LINSLEY, PS ;
WILSON, CB .
NATURE GENETICS, 1995, 11 (02) :191-197
[20]   PROLONGED AND EFFECTIVE BLOCKADE OF TUMOR-NECROSIS-FACTOR ACTIVITY THROUGH ADENOVIRUS-MEDIATED GENE-TRANSFER [J].
KOLLS, J ;
PEPPEL, K ;
SILVA, M ;
BEUTLER, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :215-219