Effective treatment of experimental glioblastoma by HSV vector-mediated TNF alpha and HSV-tk gene transfer in combination with radiosurgery and ganciclovir administration.

Experiments were carried out in a nude mouse model of human glioblastoma to determine whether gamma-knife radiosurgery combined with herpes simplex virus thymidine kinase (tk) suicide gene therapy and tumor necrosis factor alpha (TNFalpha) gene transfer provided an improved multimodality treatment of this disease. Animals were inoculated intracerebrally with 2 x 10(5) U-87MG human glioblastoma cells to establish brain tumors. At 3 days postinoculation, the tumor region was injected with 2 x 10(6) infectious particles of highly defective herpes simplex viral vectors expressing the viral tk gene with the kinetics of a viral immediate early gene either alone (T.1) or together with TNF alpha (TH:TNF). Subgroups of animals were given daily intraperitoneal injections of ganciclovir (GCV) for 10 days and/or subjected to gamma-knife radiosurgery on the fifth day post tumor-cell implantation. Comparisons of animal survival showed that the TH:TNF vector in combination with radiosurgery and GCV administration provided the most effective therapy; eight of nine animals survived for 75 days compared to four of eight using the next best protocol. These findings suggest that gene therapy in combination with more conventional therapeutic methods may provide an improved strategy for extending the life expectancy of patients afflicted with this ultimately fatal disease.

[1]  D. Gridley,et al.  Tumor necrosis factor-alpha enhances antitumor effects of radiation against glioma xenografts. , 1997, Oncology research.

[2]  F. Gage,et al.  Thymidine kinase-mediated killing of rat brain tumors. , 1993, Journal of neurosurgery.

[3]  D P Byar,et al.  Randomized comparisons of radiotherapy and nitrosoureas for the treatment of malignant glioma after surgery. , 1980, The New England journal of medicine.

[4]  Simon C Watkins,et al.  Prolonged gene expression and cell survival after infection by a herpes simplex virus mutant defective in the immediate-early genes encoding ICP4, ICP27, and ICP22 , 1996, Journal of virology.

[5]  J. Tavernier,et al.  Recombinant tumor necrosis factor can induce interleukin 2 receptor expression and cytolytic activity in a rat × mouse T cell hybrid , 1987, European journal of immunology.

[6]  Z. Ram,et al.  In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. , 1992, Science.

[7]  R. Rouse,et al.  Development of herpes simplex virus replication-defective multigene vectors for combination gene therapy applications , 1998, Gene Therapy.

[8]  B. Lulu,et al.  Stereotactic radiosurgery as an adjunct to surgery and external beam radiotherapy in the treatment of patients with malignant gliomas. , 1995, International journal of radiation oncology, biology, physics.

[9]  M. Salcman,et al.  Survival in glioblastoma: historical perspective. , 1980, Neurosurgery.

[10]  R. Crystal,et al.  Suppression of in vivo tumorigenicity of human lung cancer cells by retrovirus-mediated transfer of the human tumor necrosis factor-alpha cDNA. , 1994, American journal of respiratory cell and molecular biology.

[11]  W. Hall,et al.  Stereotactic radiosurgery for recurrent malignant gliomas. , 1995, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[12]  M. Walker,et al.  An analysis of dose-effect relationship in the radiotherapy of malignant gliomas. , 1979, International journal of radiation oncology, biology, physics.

[13]  F. Moolten Tumor chemosensitivity conferred by inserted herpes thymidine kinase genes: paradigm for a prospective cancer control strategy. , 1986, Cancer research.

[14]  Z. Ram,et al.  In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats. , 1993, Cancer research.

[15]  R. Grossman,et al.  Phase I study of adenoviral delivery of the HSV-tk gene and ganciclovir administration in patients with current malignant brain tumors. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

[16]  T. Espevik,et al.  Inhibition of cytotoxic T cell development by transforming growth factor beta and reversal by recombinant tumor necrosis factor alpha , 1987, The Journal of experimental medicine.

[17]  R. Packer,et al.  Treatment of progressive or recurrent pediatric malignant supratentorial brain tumors with herpes simplex virus thymidine kinase gene vector--producer cells followed by intravenous ganciclovir administration , 2000 .

[18]  L D Lunsford,et al.  Radiosurgery and fractionated radiation therapy: comparison of different techniques in an in vivo rat glioma model. , 1996, Journal of neurosurgery.

[19]  G. Palù,et al.  Gene therapy of glioblastoma multiforme via combined expression of suicide and cytokine genes: a pilot study in humans , 1999, Gene Therapy.

[20]  R. Ramakrishnan,et al.  Deletion of multiple immediate–early genes from herpes simplex virus reduces cytotoxicity and permits long-term gene expression in neurons , 1998, Gene Therapy.

[21]  R. Martuza,et al.  Selective killing of glioma cells in culture and in vivo by retrovirus transfer of the herpes simplex virus thymidine kinase gene. , 1991, The New biologist.

[22]  J. B. Cohen,et al.  HSV vector cytotoxicity is inversely correlated with effective TK/GCV suicide gene therapy of rat gliosarcoma , 2000, Gene Therapy.

[23]  J. B. Cohen,et al.  Connexin 43-enhanced suicide gene therapy using herpesviral vectors. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.

[24]  S. Fulda,et al.  Herpes simplex virus thymidine kinase/ganciclovir-induced apoptosis involves ligand-independent death receptor aggregation and activation of caspases. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[25]  S. Kuriyama,et al.  Complete regression of established murine hepatocellular carcinoma by in vivo tumor necrosis factor alpha gene transfer. , 1997, Gastroenterology.

[26]  E. Alexander,et al.  Radiosurgery for primary malignant brain tumors. , 1998, Seminars in surgical oncology.

[27]  J. Gutterman,et al.  Synergy of tumor necrosis factor and interleukin 2 in the activation of human cytotoxic lymphocytes: effect of tumor necrosis factor alpha and interleukin 2 in the generation of human lymphokine-activated killer cell cytotoxicity. , 1988, Cancer research.

[28]  D. Hallahan,et al.  Adenoviral TNF-α gene therapy and radiation damage tumor vasculature in a human malignant glioma xenograft , 1998, Gene Therapy.

[29]  D. Kondziolka,et al.  Survival benefit of stereotactic radiosurgery for patients with malignant glial neoplasms. , 1997, Neurosurgery.

[30]  P. Scheurich,et al.  Tumor necrosis factor enhances HLA-A,B,C and HLA-DR gene expression in human tumor cells. , 1987, Journal of immunology.

[31]  S. Moriuchi,et al.  Enhanced tumor cell killing in the presence of ganciclovir by herpes simplex virus type 1 vector-directed coexpression of human tumor necrosis factor-alpha and herpes simplex virus thymidine kinase. , 1998, Cancer research.

[32]  P. Wen,et al.  Radiosurgery as part of the initial management of patients with malignant gliomas. , 1992, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[33]  E. Alexander,et al.  Evaluation of BCNU and/or radiotherapy in the treatment of anaplastic gliomas. A cooperative clinical trial. , 1978, Journal of neurosurgery.

[34]  N. DeLuca,et al.  The herpes simplex virus immediate-early protein ICP0 affects transcription from the viral genome and infected-cell survival in the absence of ICP4 and ICP27 , 1997, Journal of virology.

[35]  P. Lipsky,et al.  Enhancement of human natural killer cell function by the combined effects of tumor necrosis factor alpha or interleukin-1 and interferon-alpha or interleukin-2. , 1989, Journal of biological response modifiers.

[36]  S. Freeman,et al.  The "bystander effect": tumor regression when a fraction of the tumor mass is genetically modified. , 1993, Cancer research.

[37]  S. Meylaerts,et al.  Bystander tumoricidal effect in the treatment of experimental brain tumors. , 1994, Neurosurgery.

[38]  N. DeLuca,et al.  Persistence and Expression of the Herpes Simplex Virus Genome in the Absence of Immediate-Early Proteins , 1998, Journal of Virology.

[39]  J. Sarkaria,et al.  Radiosurgery in the initial management of malignant gliomas: survival comparison with the RTOG recursive partitioning analysis. Radiation Therapy Oncology Group. , 1995, International journal of radiation oncology, biology, physics.