Human cancer gene therapy with cytokine gene-modified cells

被引:19
作者
Wysocki, PJ
Karczewska-Dzionk, A
Mackiewicz-Wysocka, M
Mackiewicz, A
机构
[1] Univ Med Sci, GreatPoland Canc Ctr, Dept Canc Immunol, PL-61866 Poznan, Poland
[2] Karl Marcinkowski Univ Med Sci, Dept Dermatol, Poznan, Poland
关键词
cytokines; gene-modified cancer vaccines; human gene therapy;
D O I
10.1517/14712598.4.10.1595
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cytokines can impede tumour growth and activate innate and adaptive immune responses, leading to elimination of cancer cells. For many years, it was believed that systemic administration of recombinant cytokines might become a standard treatment of different cancer types. However, due to a high toxicity of therapeutic doses and a low efficacy, even in combination with chemotherapy, this strategy is generally not accepted. On the other hand, cancer gene therapy approaches utilising cells modified with cytokine genes seem to represent a novel promising approach. For the last decade, numerous Phase I and 11 clinical trials evaluating different therapies based on cytokine gene-modified cells have been carried out. In the early studies, several strategies have been shown to improve clinical outcomes and induce strong antitumour immune responses. Recently, a few prospective, randomised, Phase III clinical trials have been initiated in order to finally determine the efficacy of particular cancer immunogene therapy strategies. This article reviews the present status and perspectives of clinical trials of cancer immunotherapies utilising cytokine gene-modified cells.
引用
收藏
页码:1595 / 1607
页数:13
相关论文
共 116 条
[71]   Cancer cells engineered to secrete granulocyte-macrophage colony-stimulating factor using ex vivo gene transfer as vaccines for the treatment of genitourinary malignancies [J].
Nelson, WG ;
Simons, JW ;
Mikhak, B ;
Chang, JF ;
DeMarzo, AM ;
Carducci, MA ;
Kim, M ;
Weber, CE ;
Baccala, AA ;
Goeman, MA ;
Clift, SM ;
Ando, DG ;
Levitsky, HI ;
Cohen, LK ;
Sanda, MG ;
Mulligan, RC ;
Partin, AW ;
Carter, HB ;
Piantadosi, S ;
Marshall, FF .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2000, 46 (Suppl 1) :S67-S72
[72]   Granulocyte-macrophage colony-stimulating factor gene-modified autologous tumor vaccines in non-small-cell lung cancer [J].
Nemunaitis, J ;
Sterman, D ;
Jablons, D ;
Smith, JW ;
Fox, B ;
Maples, P ;
Hamilton, S ;
Borellini, F ;
Lin, A ;
Morali, S ;
Hege, K .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (04) :326-331
[73]  
Nemunaitis J, 1998, CANCER GENE THER, V5, P292
[74]   Immune surveillance against a solid tumor fails because of immunological ignorance [J].
Ochsenbein, AF ;
Klenerman, P ;
Karrer, U ;
Ludewig, B ;
Pericin, M ;
Hengartner, H ;
Zinkernagel, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2233-2238
[75]  
OGASAWARA M, 1993, CANCER RES, V53, P3561
[76]   Vaccination of melanoma patients with an allogeneic, genetically modified interleukin 2-producing melanoma cell line [J].
Osanto, S ;
Schiphorst, PP ;
Weijl, NI ;
Dijkstra, N ;
Van Wees, A ;
Brouwenstein, N ;
Vaessen, N ;
Van Krieken, JHJM ;
Hermans, J ;
Cleton, FJ ;
Schrier, PI .
HUMAN GENE THERAPY, 2000, 11 (05) :739-750
[77]   The designer cytokine hyper-IL-6 mediates growth inhibition and GM-CSF-dependent rejection of B16 melanoma cells [J].
Özbek, S ;
Peters, M ;
Breuhahn, K ;
Mann, A ;
Blessing, M ;
Fischer, M ;
Schirmacher, P ;
Mackiewicz, A ;
Rose-John, S .
ONCOGENE, 2001, 20 (08) :972-979
[78]   Gene therapy with autologous, interleukin 2-secreting tumor cells in patients with malignant melanoma [J].
Palmer, K ;
Moore, J ;
Everard, M ;
Harris, JD ;
Rodgers, S ;
Rees, RC ;
Murray, AK ;
Mascari, R ;
Kirkwood, J ;
Riches, PG ;
Fisher, C ;
Thomas, JM ;
Harries, M ;
Johnston, SRD ;
Collins, MKL ;
Gore, ME .
HUMAN GENE THERAPY, 1999, 10 (08) :1261-1268
[79]   Intensity of the vaccine-elicited immune response determines tumor clearance [J].
Perez-Diez, A ;
Spiess, PJ ;
Restifo, NP ;
Matzinger, P ;
Marincola, FM .
JOURNAL OF IMMUNOLOGY, 2002, 168 (01) :338-347
[80]  
PERICLE F, 1994, J IMMUNOL, V153, P5659