Mesenchymal progenitor cells as cellular vehicles for delivery of oncolytic adenoviruses

被引:238
作者
Komarova, S
Kawakami, Y
Stoff-Khalili, MA
Curiel, DT
Pereboeva, L
机构
[1] Univ Alabama, Gene Therapy Ctr, Div Human Gene Therapy, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Pathol, Div Human Gene Therapy, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Surg, Div Human Gene Therapy, Birmingham, AL 35294 USA
[4] Univ Dusseldorf, Ctr Med, Dept Obstet, D-4000 Dusseldorf, Germany
[5] Univ Dusseldorf, Ctr Med, Dept Gynecol, D-4000 Dusseldorf, Germany
关键词
D O I
10.1158/1535-7163.MCT-05-0334
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Natural and genetically modified oncolytic viruses have been systematically tested as anticancer therapeutics. Among this group, conditionally replicative adenoviruses have been developed for a broad range of tumors with a rapid transition to clinical settings. Unfortunately, clinical trials have shown limited antitumor efficacy partly due to insufficient viral delivery to tumor sites. We investigated the possibility of using mesenchymal progenitor cells (MPC) as virus carriers based on the documented tumor-homing abilities of this cell population. We confirmed preferential tumor homing of MPCs in an animal model of ovarian carcinoma and evaluated the capacity of MPCs to be loaded with oncolytic adenoviruses. We showed that MPCs were efficiently infected with an adenovirus genetically modified for coxsackie and adenovirus receptor-independent infection (Ad5/3), which replicated in the cell carriers. MPCs loaded with Ad5/3 caused total cell killing when cocultured with a cancer cell line. In an animal model of ovarian cancer, MPC-based delivery of the Ad5/3 increased the survival of tumor-bearing mice compared with direct viral injection. Further, tumor imaging confirmed a decrease in tumor burden in animals treated with oncolytic virus delivered by MPC carriers compared with the direct injection of the adenovirus. These data show that MPCs can serve as intermediate carriers for replicative adenoviruses and suggest that the natural homing properties of specific cell types can be used for targeted delivery of these virions.
引用
收藏
页码:755 / 766
页数:12
相关论文
共 51 条
  • [1] CAR-binding ablation does not change biodistribution and toxicity of adenoviral vectors
    Alemany, R
    Curiel, DT
    [J]. GENE THERAPY, 2001, 8 (17) : 1347 - 1353
  • [2] Dynamic of distribution of human bone marrow-derived mesenchymal stem cells after transplantation into adult unconditioned mice
    Allers, C
    Sierralta, WD
    Neubauer, S
    Rivera, F
    Minguell, JJ
    Conget, PA
    [J]. TRANSPLANTATION, 2004, 78 (04) : 503 - 508
  • [3] Bauerschmitz GJ, 2002, CANCER RES, V62, P1266
  • [4] Bone marrow stromal stem cells: Nature, biology, and potential applications
    Bianco, P
    Riminucci, M
    Gronthos, S
    Robey, PG
    [J]. STEM CELLS, 2001, 19 (03) : 180 - 192
  • [5] Tumor antigen-specific induction of transcriptionally targeted retroviral vectors from chimeric immune receptor-modified T cells
    Chester, J
    Ruchatz, A
    Gough, M
    Crittenden, M
    Chong, H
    Loïc-Cosset, L
    Diaz, RM
    Harrington, K
    Alvarez-Vallina, L
    Vile, R
    [J]. NATURE BIOTECHNOLOGY, 2002, 20 (03) : 256 - 263
  • [6] Adenoviral-mediated gene transfer into ex vivo expanded human bone marrow mesenchymal progenitor cells
    Conget, PA
    Minguell, JJ
    [J]. EXPERIMENTAL HEMATOLOGY, 2000, 28 (04) : 382 - 390
  • [7] Coukos G, 1999, CLIN CANCER RES, V5, P1523
  • [8] Crittenden M, 2003, CANCER RES, V63, P3173
  • [9] PEGylation of E1-deleted adenovirus vectors allows significant gene expression on readministration to liver
    Croyle, MA
    Chirmule, N
    Zhang, Y
    Wilson, JM
    [J]. HUMAN GENE THERAPY, 2002, 13 (15) : 1887 - 1900
  • [10] Infectivity-enhanced cyclooxygenase-2-based conditionally replicative adenoviruses for esophageal adenocarcinoma treatment
    Davydova, J
    Le, LP
    Gavrikova, T
    Wang, MH
    Krasnykh, V
    Yamamoto, M
    [J]. CANCER RESEARCH, 2004, 64 (12) : 4319 - 4327