Replicating viral vectors for cancer therapy: strategies to synergize with host immune responses

被引:12
作者
Altomonte, Jennifer [1 ]
Ebert, Oliver [1 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Med Klin & Poliklin 2, D-8000 Munich, Germany
关键词
VESICULAR STOMATITIS-VIRUS; NEWCASTLE-DISEASE-VIRUS; HERPES-SIMPLEX-VIRUS; ONCOLYTIC MEASLES-VIRUS; T-CELL THERAPY; PHASE-I TRIAL; ANTITUMOR EFFICACY; DENDRITIC CELLS; GM-CSF; HEPATOCELLULAR-CARCINOMA;
D O I
10.1111/j.1751-7915.2011.00296.x
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
Tumour-specific replicating (oncolytic) viruses are novel anticancer agents, currently under intense investigation in preclinical studies and phase IIII clinical trials. Until recently, most studies have focused on the direct antitumour properties of these viruses. There is now an increasing body of evidence indicating that host immune responses may be critical to the efficacy of oncolytic virotherapy. Although the immune response to oncolytic viruses can rapidly restrict viral replication, thereby limiting the efficacy of therapy, oncolytic virotherapy also has the potential to induce potent antitumoural immune effectors that destroy those cancer cells, which are not directly lysed by virus. In this review, we discuss the role of the immune system in terms of antiviral and antitumoural responses, as well as strategies to evade or promote these responses in favour of improved therapeutic potentials.
引用
收藏
页码:251 / 259
页数:9
相关论文
共 68 条
[1]   Viral mimicry of cytokines, chemokines and their receptors [J].
Alcami, A .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (01) :36-50
[2]   Enhanced oncolytic potency of vesicular stomatitis virus through vector-mediated inhibition of NK and NKT cells [J].
Altomonte, J. ;
Wu, L. ;
Meseck, M. ;
Chen, L. ;
Ebert, O. ;
Garcia-Sastre, A. ;
Fallon, J. ;
Mandeli, J. ;
Woo, S. L. C. .
CANCER GENE THERAPY, 2009, 16 (03) :266-278
[3]   Exponential enhancement of oncolytic vesicular stomatitis virus potency by vector-mediated suppression of inflammatory responses in vivo [J].
Altomonte, Jennifer ;
Wu, Lan ;
Chen, Li ;
Meseck, Marcia ;
Ebert, Oliver ;
Garcia-Sastre, Adolfo ;
Fallon, John ;
Woo, Savio L. C. .
MOLECULAR THERAPY, 2008, 16 (01) :146-153
[4]   HSV oncolytic therapy upregulates interferon-inducible chemokines and recruits immune effector cells in ovarian cancer [J].
Benencia, F ;
Courrèges, MC ;
Conejo-García, JR ;
Mohamed-Hadley, A ;
Zhang, L ;
Buckanovich, RJ ;
Carroll, R ;
Fraser, N ;
Coukos, G .
MOLECULAR THERAPY, 2005, 12 (05) :789-802
[5]   Targeted inflammation during oncolytic virus therapy severely compromises tumor blood flow [J].
Breitbach, Caroline J. ;
Paterson, Jennifer M. ;
Lemay, Chantal G. ;
Falls, Theresa J. ;
McGuire, Allison ;
Parato, Kelley A. ;
Stojdl, David F. ;
Daneshmand, Manijeh ;
Speth, Kelly ;
Kirn, David ;
McCart, J. Andrea ;
Atkins, Harold ;
Bell, John C. .
MOLECULAR THERAPY, 2007, 15 (09) :1686-1693
[6]   Potentiating Cancer Immunotherapy Using an Oncolytic Virus [J].
Bridle, Byram W. ;
Stephenson, Kyle B. ;
Boudreau, Jeanette E. ;
Koshy, Sandeep ;
Kazdhan, Natasha ;
Pullenayegum, Eleanor ;
Brunelliere, Jerome ;
Bramson, Jonathan L. ;
Lichty, Brian D. ;
Wan, Yonghong .
MOLECULAR THERAPY, 2010, 18 (08) :1430-1439
[7]   CD4+ T helper cell-independent antitumor response mediated by murine IFN-β gene delivery in immunocompetent mice [J].
Brown, JL ;
Barsoum, J ;
Qin, XQ .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2002, 22 (06) :719-728
[8]   Oncolytic Adenovirus Coding for Granulocyte Macrophage Colony-Stimulating Factor Induces Antitumoral Immunity in Cancer Patients [J].
Cerullo, Vincenzo ;
Pesonen, Sari ;
Diaconu, Iulia ;
Escutenaire, Sophie ;
Arstila, Petteri T. ;
Ugolini, Matteo ;
Nokisalmi, Petri ;
Raki, Mari ;
Laasonen, Leena ;
Sarkioja, Merja ;
Rajecki, Maria ;
Kangasniemi, Lotta ;
Guse, Kilian ;
Helminen, Andreas ;
Ahtiainen, Laura ;
Ristimaki, Ari ;
Raisanen-Sokolowski, Anne ;
Haavisto, Elina ;
Oksanen, Minna ;
Karli, Eerika ;
Karioja-Kallio, Aila ;
Holm, Sirkka-Liisa ;
Kouri, Mauri ;
Joensuu, Timo ;
Kanerva, Anna ;
Hemminki, Akseli .
CANCER RESEARCH, 2010, 70 (11) :4297-4309
[9]   E1A-expressing adenoviral E3B mutants act synergistically with chemotherapeutics in immunocompetent tumor models [J].
Cheong, S. C. ;
Wang, Y. ;
Meng, J-H ;
Hill, R. ;
Sweeney, K. ;
Kirn, D. ;
Lemoine, N. R. ;
Hallden, G. .
CANCER GENE THERAPY, 2008, 15 (01) :40-50
[10]   A phase I open-label, dose-escalation, multi-institutional trial of injection with an E1B-attenuated adenovirus, ONYX-015, into the peritumoral region of recurrent malignant gliomas, in the adjuvant setting [J].
Chiocca, EA ;
Abbed, KM ;
Tatter, S ;
Louis, DN ;
Hochberg, FH ;
Barker, F ;
Kracher, J ;
Grossman, SA ;
Fisher, JD ;
Carson, K ;
Rosenblum, M ;
Mikkelsen, T ;
Olson, J ;
Markert, J ;
Rosenfeld, S ;
Nabors, LB ;
Brem, S ;
Phuphanich, S ;
Freeman, S ;
Kaplan, R ;
Zwiebel, J .
MOLECULAR THERAPY, 2004, 10 (05) :958-966