Multi-modal combination gene therapy for malignant glioma using replication-defective HSV vectors

被引:9
|
作者
Burton, EA [1 ]
Glorioso, JC [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
关键词
D O I
10.1016/S1359-6446(01)01713-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Herpes simplex virus (HSV) may be modified to produce a nonpathogenic vector that is capable of delivering multiple transgenes simultaneously to cells, both safely and efficiently. We have exploited this property to develop viruses that target glioblastoma, a malignancy that is currently associated with a poor prognosis. Using rationally selected combinations of therapeutic transgenes coupled with gamma-knife radiotherapy, the ablation of experimental tumours in animal models has been demonstrated. Combination gene therapy using replication-defective HSV vectors represents a promising and exciting approach to tackling malignancy in the CNS.
引用
收藏
页码:347 / 356
页数:10
相关论文
共 50 条
  • [41] ECTOPIC EXPRESSION OF GENES DURING CHICKEN LIMB PATTERN-FORMATION USING REPLICATION-DEFECTIVE RETROVIRAL VECTORS
    DELAPOMPA, JL
    ZELLER, R
    MECHANISMS OF DEVELOPMENT, 1993, 43 (2-3) : 187 - 198
  • [42] Estimating the Prognosis of Low-Grade Glioma with Gene Attention Using Multi-Omics and Multi-Modal Schemes
    Choi, Sanghyuk Roy
    Lee, Minhyeok
    BIOLOGY-BASEL, 2022, 11 (10):
  • [43] Recombinant, replication-defective adenovirus gene transfer vectors induce cell cycle dysregulation and inappropriate expression of cyclin proteins
    Wersto, RP
    Rosenthal, ER
    Seth, PK
    Eissa, NT
    Donahue, RE
    JOURNAL OF VIROLOGY, 1998, 72 (12) : 9491 - 9502
  • [44] Inhibition of Repair of Radiation-Induced DNA Damage Enhances Gene Expression from Replication-Defective Adenoviral Vectors
    Hingorani, Mohan
    White, Christine L.
    Merron, Andrew
    Peerlinck, Inge
    Gore, Martin E.
    Slade, Andrew
    Scott, Simon D.
    Nutting, Christopher M.
    Pandha, Hardev S.
    Melcher, Alan A.
    Vile, Richard G.
    Vassaux, Georges
    Harrington, Kevin J.
    CANCER RESEARCH, 2008, 68 (23) : 9771 - 9778
  • [45] EFFICIENT CATHETER-MEDIATED GENE-TRANSFER INTO THE HEART USING REPLICATION-DEFECTIVE ADENOVIRUS
    BARR, E
    CARROLL, J
    KALYNYCH, AM
    TRIPATHY, SK
    KOZARSKY, K
    WILSON, JM
    LEIDEN, JM
    GENE THERAPY, 1994, 1 (01) : 51 - 58
  • [46] EFFICIENT CATHETER-MEDIATED GENE-TRANSFER INTO THE HEART USING REPLICATION-DEFECTIVE ADENOVIRUS
    BARR, E
    TRIPATHY, SK
    KOZARSKY, K
    WILSON, JM
    CARROLL, JD
    LEIDEN, JM
    CIRCULATION, 1993, 88 (04) : 475 - 475
  • [47] Secretion of human recombinant factor IX from cells of adipose, myogenic and hepatic origin transduced with replication-defective HSV-1 genomic vectors
    Fradette, J
    Flanigan, R
    Krisky, DM
    Goins, WF
    Glorioso, JC
    MOLECULAR THERAPY, 2004, 9 : S63 - S63
  • [48] Intraoperative Glioma Grading Using Neural Architecture Search and Multi-Modal Imaging
    Xiao, Anqi
    Shen, Biluo
    Shi, Xiaojing
    Zhang, Zhe
    Zhang, Zeyu
    Tian, Jie
    Ji, Nan
    Hu, Zhenhua
    IEEE TRANSACTIONS ON MEDICAL IMAGING, 2022, 41 (10) : 2570 - 2581
  • [49] Transgene expression in malignant glioma using a replication-defective adenoviral vector containing the Egr-1 promoter:: Activation by ionizing radiation or uptake of radioactive iododeoxyuridine
    Manome, Y
    Kunieda, T
    Wen, PY
    Koga, T
    Kufe, DW
    Ohno, T
    HUMAN GENE THERAPY, 1998, 9 (10) : 1409 - 1417
  • [50] Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors
    Tripathy, SK
    Black, HB
    Goldwasser, E
    Leiden, JM
    NATURE MEDICINE, 1996, 2 (05) : 545 - 550