Expressing human interleukin-15 from oncolytic vesicular stomatitis virus improves survival in a murine metastatic colon adenocarcinoma model through the enhancement of anti-tumor immunity

被引:90
作者
Stephenson, K. B. [1 ]
Barra, N. G. [1 ]
Davies, E. [1 ]
Ashkar, A. A. [1 ]
Lichty, B. D. [1 ]
机构
[1] McMaster Univ, Dept Pathol & Mol Med, Ctr Gene Therapeut, McMaster Immunol Res Ctr, Hamilton, ON L8S 4K1, Canada
关键词
oncolytic virus; VSV; IL-15; colon cancer; CD8(+) T-CELLS; CANCER THERAPEUTICS; IL-15; ACTIVITY; IN-VIVO; IMMUNOTHERAPY; THERAPY; NK; ACTIVATION; TUMORS; MICE;
D O I
10.1038/cgt.2011.81
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
In this study, we sought to enhance the potency of an oncolytic virus, vesicular stomatitis virus (VSV), by inserting a transgene encoding a highly secreted version of human interleukin-15 (IL-15). IL-15 has shown promise as an immunotherapeutic cytokine, as it is able to enhance both natural killer (NK) and T-cell responses, but it has not yet been tested as a therapeutic transgene in the context of viral oncolysis. The transgene was modified to ensure enhanced secretion of IL-15 from infected cells, leading to strong localized expression from infected CT-26 tumors in vivo. This localized expression in the tumor microenvironment led to a clear enhancement to anti-tumoral T-cell responses and enhanced survival, while additional IL-15 administration systemically failed to further enhance the therapy. Overall, the transient localized expression of IL-15 in the tumour by an oncolytic virus was able to induce stronger anti-tumoral immunity in a murine model of colon carcinoma. Cancer Gene Therapy (2012) 19, 238-246; doi:10.1038/cgt.2011.81; published online 9 December 2011
引用
收藏
页码:238 / 246
页数:9
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