Intracerebral injection of adenovirus harboring the HSVtk gene combined with ganciclovir administration: toxicity study in nonhuman primates

被引:24
作者
Driesse, MJ
Vincent, AJPE
Smitt, PAES
Kros, JM
Hoogerbrugge, PM
Avezaat, CJJ
Valerio, D
Bout, A
机构
[1] Univ Rotterdam Hosp, Dept Neurosurg, Leiden, Netherlands
[2] Univ Rotterdam Hosp, Dept Neurooncol, Leiden, Netherlands
[3] Univ Rotterdam Hosp, Dept Neuropathol, Leiden, Netherlands
[4] Univ Leiden Hosp, Dept Pediat, Div Hematol, NL-2300 RC Leiden, Netherlands
[5] Leiden Univ, Dept Mol Cell Biol, Leiden, Netherlands
[6] IntroGene BV, Leiden, Netherlands
关键词
recombinant adenovirus; HSVtk; gene therapy; toxicity; brain tumors;
D O I
10.1038/sj.gt.3300695
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A high dose (1-2.5x 10(10) infectious units) of recombinant gene (IG.Ad.MLPI.TK) was injected into the white matter adenovirus harboring the herpes simplex thymidine kinase of the right frontal lobe in two rhesus monkeys (M. mulatta). injection of the vector was followed by systemic ganciclovir administration (10 mg/kg per day) for 14 days. During treatment no clinical symptoms were observed. Histopathological analysis of the brain at day 18 showed a 5 mm necrotic area at the site of the virus injection. This area was invaded and surrounded by inflammatory cells and activated astrocytes (gliosis). Immunohistochemical analysis of the infiltrates revealed the presence of predominantly mononuclear cells. In the vicinity of the lesion perivascular cuffs were seen containing T lymphocytes and clusters of B lymphocytes. From this preclinical study we conclude that the toxicity of adenotk/GCV is acceptable and treatment of patients with malignant gliomas using this kind of therapy is feasible. However, careful dose finding in clinical studies is recommended.
引用
收藏
页码:1122 / 1129
页数:8
相关论文
共 53 条
[31]   DEFECTIVE AND NONDEFECTIVE ADENOVIRUS VECTORS FOR EXPRESSING FOREIGN GENES INVITRO AND INVIVO [J].
LEVRERO, M ;
BARBAN, V ;
MANTECA, S ;
BALLAY, A ;
BALSAMO, C ;
AVANTAGGIATI, ML ;
NATOLI, G ;
SKELLEKENS, H ;
TIOLLAIS, P ;
PERRICAUDET, M .
GENE, 1991, 101 (02) :195-202
[32]   ADENOVIRUS TRIPARTITE LEADER SEQUENCE ENHANCES TRANSLATION OF MESSENGER-RNAS LATE AFTER INFECTION [J].
LOGAN, J ;
SHENK, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (12) :3655-3659
[33]  
Maron A, 1996, GENE THER, V3, P315
[34]   Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins [J].
Mesnil, M ;
Piccoli, C ;
Tiraby, G ;
Willecke, K ;
Yamasaki, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (05) :1831-1835
[35]   Adenovirus-mediated gene transfer: Influence of transgene, mouse strain and type of immune response on persistence of transgene expression [J].
Michou, AI ;
Santoro, L ;
Christ, M ;
Julliard, V ;
Pavirani, A ;
Mehtali, M .
GENE THERAPY, 1997, 4 (05) :473-482
[36]  
MOOLTEN FL, 1986, CANCER RES, V46, P5276
[37]   Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: Comparison of E2a wild type and E2a deleted vectors [J].
Morral, N ;
ONeal, W ;
Zhou, HS ;
Langston, C ;
Beaudet, A .
HUMAN GENE THERAPY, 1997, 8 (10) :1275-1286
[38]   ADENOVIRUS-MEDIATED GENE-THERAPY OF EXPERIMENTAL GLIOMAS [J].
PEREZCRUET, MJ ;
TRASK, TW ;
CHEN, SH ;
GOODMAN, JC ;
WOO, SLC ;
GROSSMAN, RG ;
SHINE, HD .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 39 (04) :506-511
[39]  
Precious B., 1985, VIROLOGY PRACTICAL A, P193
[40]  
Ramesh R, 1996, EXP HEMATOL, V24, P829