Genetically engineered Newcastle disease virus expressing interleukin 2 is a potential drug candidate for cancer immunotherapy

被引:45
作者
Bai, Fuliang [1 ]
Niu, Zeshan [1 ]
Tian, Hui [1 ]
Li, Siming [1 ]
Lv, Zheng [1 ]
Zhang, Tianyuan [1 ]
Ren, Guiping [1 ]
Li, Deshan [1 ]
机构
[1] Northeast Agr Univ, Biopharmaceut Teaching & Res Sect, Coll Life Sci, Harbin 150030, Peoples R China
关键词
NDV; IL2; rLaSota/IL2; Cancer therapy; Immunotherapy; Oncolytic therapy; PRIMARY LIVER-CANCER; ONCOLYTIC VIRUS; MALIGNANT-MELANOMA; RECOMBINANT INTERLEUKIN-2; HEPATOCELLULAR-CARCINOMA; GLIOBLASTOMA-MULTIFORME; ANTITUMOR VACCINATION; IMMUNE-RESPONSES; TUMOR-CELLS; IN-VIVO;
D O I
10.1016/j.imlet.2014.02.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Newcastle disease virus (NDV) is an intrinsically tumor-specific virus, several clinical trials have reported that mesogenic NDV is a safe and effective agent for human cancer therapy. Interleukin 2 (IL2) is a cytokine that stimulates T cell propagation to trigger innate and adaptive immunity. IL2 has been used for cancer therapy and has achieved curative effects. In this study, a recombinant NDV LaSota strain expressing human interleukin 2 (rLaSota/IL2) was generated. The ability of rLaSota/IL2 to express human IL2 was detected in the infected tumor cells. In addition, the activity of IL2 was analyzed. The antitumor potential of rLaSota/IL2 was studied by xenograph mice carrying H22 and B16-F10 cells. Tumor-specific CD4(+) and CD8(+) T cells and MHC II were also analyzed in the two tumor-bearing models. Our study showed that rLaSota/IL2 significantly stimulated tumor-specific cytotoxic T-lymphocyte (CTL) responses and increased regulatory CD4(+) and cytotoxic CD8(+) T cells proliferation. The treatment with rLaSota/IL2 led to tumor regression in tumor-bearing mice and prolonged the survival of tumor-bearing mice. Furthermore, tumor challenging experiments demonstrated that rLaSota/IL2 invoked mice a unique capacity to remember a pathogen through the generation of memory T cells, which protect the host in the event of reinfection and form adaptive immune system. The result indicates that tumor-infiltrating CD4(+) T regulatory cells may denote the effective regression of tumors. Taken together, rLaSota/IL2 has potential for immunotherapy and oncolytic therapy of cancers and may be an ideal candidate for clinical application in future cancer therapy. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:36 / 46
页数:11
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