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表达人白细胞介素-15 的溶瘤单纯疱疹病毒通过增强抗肿瘤免疫提高转移性结肠腺癌小鼠模型的存活率。

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.

机构信息

Department of Pathology and Molecular Medicine, Centre for Gene Therapeutics, McMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.

出版信息

Cancer Gene Ther. 2012 Apr;19(4):238-46. doi: 10.1038/cgt.2011.81. Epub 2011 Dec 9.

Abstract

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.

摘要

在这项研究中,我们试图通过插入一个编码人白细胞介素-15(IL-15)的高分泌版本的转基因来增强溶瘤病毒水疱性口炎病毒(VSV)的效力。IL-15 作为一种免疫治疗细胞因子具有很大的潜力,因为它能够增强自然杀伤(NK)和 T 细胞的反应,但尚未在病毒溶瘤的背景下作为治疗性转基因进行测试。该转基因经过修饰,以确保从感染细胞中增强 IL-15 的分泌,从而导致体内感染 CT-26 肿瘤的局部强烈表达。这种在肿瘤微环境中的局部表达导致抗肿瘤 T 细胞反应明显增强和生存时间延长,而全身性给予额外的 IL-15 则未能进一步增强治疗效果。总的来说,溶瘤病毒在肿瘤中的瞬时局部表达能够在结直肠癌的小鼠模型中诱导更强的抗肿瘤免疫。

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