Group D adenoviruses infect primary central nervous system cells more efficiently than those from group C

被引:60
作者
Chillon, M
Bosch, A
Zabner, J
Law, L
Armentano, D
Welsh, MJ
Davidson, BL
机构
[1] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[3] Genzyme Corp, Framingham, MA 01701 USA
关键词
D O I
10.1128/JVI.73.3.2537-2540.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Group C adenovirus-mediated gene transfer to central nervous system cells is inefficient. We found that wild-type group D viruses, or recombinant adenovirus type 2 (Ad2) (group C) modified to contain Ad17 (group D) fiber, were more efficient in infecting primary cultures of neurons. Together with studies on primary vascular endothelial cells and tissue culture cell lines, our results indicate that there is not a universally applicable adenovirus serotype for use as a gene transfer vector.
引用
收藏
页码:2537 / 2540
页数:4
相关论文
共 34 条
  • [1] Effect of the E4 region on the persistence of transgene expression from adenovirus vectors
    Armentano, D
    Zabner, J
    Sacks, C
    Sookdeo, CC
    Smith, MP
    StGeorge, JA
    Wadsworth, SC
    Smith, AE
    Gregory, RJ
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (03) : 2408 - 2416
  • [2] Poly(lactic-glycolic) acid copolymer encapsulation of recombinant adenovirus reduces immunogenicity in vivo
    Beer, SJ
    Matthews, CB
    Stein, CS
    Ross, BD
    Hilfinger, JM
    Davidson, BL
    [J]. GENE THERAPY, 1998, 5 (06) : 740 - 746
  • [3] Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5
    Bergelson, JM
    Cunningham, JA
    Droguett, G
    KurtJones, EA
    Krithivas, A
    Hong, JS
    Horwitz, MS
    Crowell, RL
    Finberg, RW
    [J]. SCIENCE, 1997, 275 (5304) : 1320 - 1323
  • [4] ATTENUATION OF STROKE SIZE IN RATS USING AN ADENOVIRAL VECTOR TO INDUCE OVEREXPRESSION OF INTERLEUKIN-1 RECEPTOR ANTAGONIST IN BRAIN
    BETZ, AL
    YANG, GY
    DAVIDSON, BL
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1995, 15 (04) : 547 - 551
  • [5] Byrnes AP, 1996, GENE THER, V3, P644
  • [6] ADENOVIRUS GENE-TRANSFER CAUSES INFLAMMATION IN THE BRAIN
    BYRNES, AP
    RUSBY, JE
    WOOD, MJA
    CHARLTON, HM
    [J]. NEUROSCIENCE, 1995, 66 (04) : 1015 - 1024
  • [7] Dopaminergic neurons protected from degeneration by GDNF gene therapy
    ChoiLundberg, DL
    Lin, Q
    Chang, YN
    Chiang, YL
    Hay, CM
    Mohajeri, H
    Davidson, BL
    Bohn, MC
    [J]. SCIENCE, 1997, 275 (5301) : 838 - 841
  • [8] Recombinant adenovirus: A gene transfer vector for study and treatment of CNS diseases
    Davidson, BL
    Bohn, MC
    [J]. EXPERIMENTAL NEUROLOGY, 1997, 144 (01) : 125 - 130
  • [9] EXPRESSION OF ESCHERICHIA-COLI BETA-GALACTOSIDASE AND RAT HPRT IN THE CNS OF MACACA-MULATTA FOLLOWING ADENOVIRAL MEDIATED GENE-TRANSFER
    DAVIDSON, BL
    DORAN, SE
    SHEWACH, DS
    LATTA, JM
    HARTMAN, JW
    ROESSLER, BJ
    [J]. EXPERIMENTAL NEUROLOGY, 1994, 125 (02) : 258 - 267
  • [10] A MODEL SYSTEM FOR INVIVO GENE-TRANSFER INTO THE CENTRAL-NERVOUS-SYSTEM USING AN ADENOVIRAL VECTOR
    DAVIDSON, BL
    ALLEN, ED
    KOZARSKY, KF
    WILSON, JM
    ROESSLER, BJ
    [J]. NATURE GENETICS, 1993, 3 (03) : 219 - 223