Strategies to Optimise Oncolytic Viral Therapies: The Role of Natural Killer Cells

被引:4
作者
Leung, Elaine Y. L. [1 ]
McNeish, Iain A. [2 ]
机构
[1] Univ Birmingham, Coll Med & Dent Sci, Inst Canc & Genom Sci, Birmingham B15 2TT, W Midlands, England
[2] Imperial Coll London, Ovarian Canc Action Res Ctr, Dept Surg & Canc, IRDB Bldg, London W12 0NN, England
来源
VIRUSES-BASEL | 2021年 / 13卷 / 08期
关键词
oncolytic virus; NK cells; immunotherapy; gene therapy; neoplasms; HUMAN DENDRITIC CELLS; HERPES-SIMPLEX-VIRUS; NK-CELLS; GLIOBLASTOMA VIROTHERAPY; SYSTEMIC DELIVERY; PERIPHERAL-BLOOD; CANCER; TUMORS; RECEPTOR; REOVIRUS;
D O I
10.3390/v13081450
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oncolytic viruses (OVs) are an emerging class of anti-cancer agents that replicate selectively within malignant cells and generate potent immune responses. Their potential efficacy has been shown in clinical trials, with talimogene laherparepvec (T-VEC or IMLYGIC((R))) now approved both in the United States and Europe. In healthy individuals, NK cells provide effective surveillance against cancer and viral infections. In oncolytic viral therapy, NK cells may render OV ineffective by rapid elimination of the propagating virus but could also improve therapeutic efficacy by preferential killing of OV-infected malignant cells. Existing evidence suggests that the overall effect of NK cells against OV is context dependent. In the past decade, the understanding of cancer and OV biology has improved significantly, which helped refine this class of treatments in early-phase clinical trials. In this review, we summarised different strategies that have been evaluated to modulate NK activities for improving OV therapeutic benefits. Further development of OVs will require a systematic approach to overcome the challenges of the production and delivery of complex gene and cell-based therapies in clinical settings.
引用
收藏
页数:12
相关论文
共 98 条
[51]  
Ishigami S, 2000, CANCER, V88, P577, DOI 10.1002/(SICI)1097-0142(20000201)88:3<577::AID-CNCR13>3.3.CO
[52]  
2-M
[53]   Influenza Virus Infection Enhances Antibody-Mediated NK Cell Functions via Type I Interferon-Dependent Pathways [J].
Jegaskanda, Sinthujan ;
Vanderven, Hillary A. ;
Tan, Hyon-Xhi ;
Alcantara, Sheilajen ;
Wragg, Kathleen M. ;
Parsons, Matthew S. ;
Chung, Amy W. ;
Juno, Jennifer A. ;
Kent, Stephen J. .
JOURNAL OF VIROLOGY, 2019, 93 (05)
[54]   Potentiating Oncolytic Virus-Induced Immune-Mediated Tumor Cell Killing Using Histone Deacetylase Inhibition [J].
Jennings, Victoria A. ;
Scott, Gina B. ;
Rose, Ailsa M. S. ;
Scott, Karen J. ;
Migneco, Gemma ;
Keller, Brian ;
Reilly, Katrina ;
Donnelly, Oliver ;
Peach, Howard ;
Dewar, Donald ;
Harrington, Kevin J. ;
Pandha, Hardev ;
Samson, Adel ;
Vile, Richard G. ;
Melcher, Alan A. ;
Errington-Mais, Fiona .
MOLECULAR THERAPY, 2019, 27 (06) :1139-1152
[55]   Control of Human Viral Infections by Natural Killer Cells [J].
Jost, Stephanie ;
Altfeld, Marcus .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 31, 2013, 31 :163-194
[56]   History of oncolytic viruses: Genesis to genetic engineering [J].
Kelly, Elizabeth ;
Russell, Stephen J. .
MOLECULAR THERAPY, 2007, 15 (04) :651-659
[57]   Biological treatment of pediatric sarcomas by combined virotherapy and NK cell therapy [J].
Klose, Chihab ;
Berchtold, Susanne ;
Schmidt, Marina ;
Beil, Julia ;
Smirnow, Irina ;
Venturelli, Sascha ;
Burkard, Markus ;
Handgretinger, Rupert ;
Lauer, Ulrich M. .
BMC CANCER, 2019, 19 (01)
[58]   Use of Biological Therapy to Enhance Both Virotherapy and Adoptive T-Cell Therapy for Cancer [J].
Kottke, Timothy ;
Diaz, Rosa M. ;
Kaluza, Karen ;
Pulido, Jose ;
Galivo, Feorillo ;
Wongthida, Phonphimon ;
Thompson, Jill ;
Willmon, Candice ;
Barber, Glen N. ;
Chester, John ;
Selby, Peter ;
Strome, Scott ;
Harrington, Kevin ;
Melcher, Alan ;
Vile, Richard G. .
MOLECULAR THERAPY, 2008, 16 (12) :1910-1918
[59]   Improved Systemic Delivery of Oncolytic Reovirus to Established Tumors Using Preconditioning with Cyclophosphamide-Mediated Treg Modulation and Interleukin-2 [J].
Kottke, Timothy ;
Thompson, Jill ;
Diaz, Rosa Maria ;
Pulido, Jose ;
Willmon, Candice ;
Coffey, Matt ;
Selby, Peter ;
Melcher, Alan ;
Harrington, Kevin ;
Vile, Richard G. .
CLINICAL CANCER RESEARCH, 2009, 15 (02) :561-569
[60]   Superagonist IL-15-Armed Oncolytic Virus Elicits Potent Antitumor Immunity and Therapy That Are Enhanced with PD-1 Blockade [J].
Kowalsky, Stacy J. ;
Liu, Zuqiang ;
Feist, Mathilde ;
Berkey, Sara E. ;
Ma, Congrong ;
Ravindranathan, Roshni ;
Dai, Enyong ;
Roy, Edward J. ;
Guo, Zong Sheng ;
Bartlett, David L. .
MOLECULAR THERAPY, 2018, 26 (10) :2476-2486