Laboratory of Microbiology and Immunology, College of Pharmacy, Kangwon National University, Chuncheon, 200-701, South Korea.
Vaccine. 2013 Feb 27;31(10):1377-84. doi: 10.1016/j.vaccine.2013.01.006. Epub 2013 Jan 11.
Attenuated Salmonella vaccines show therapeutic anti-cancer effects, but the underlying mechanism has not been well investigated. In the current study, intratumoral (i.t.) injection of recombinant attenuated Salmonella enterica serovar Typhimurium vaccine (RASV) significantly inhibited Her-2/neu-expressing tumor growth. Although depletion of CD8(+) cells in RASV-treated mice significantly restored tumor growth, the induction of Her-2/neu-specific cytotoxic T lymphocytes (CTLs) was not well correlated with the generation of the anti-tumor effect. Therefore, we hypothesized that RASV might induce a tumor microenvironmental shift, from immune suppressive to immunogenic, to reduce the suppressive force and finally elicit a successful anti-tumor response. We found that i.t. injection of RASV significantly increased the level of CD11b(+)Gr-1(+) myeloid cells identified as myeloid-derived suppressor cell (MDSC), but a significant portion of these cells were TNF-α-secreting Ly6-G(high) subsets, which can function as antitumor effector cells. We further investigated whether RASV can modulate immunosuppressive Treg cells, and CD4(+)CD25(+) Foxp3(+) Tregs was significantly reduced in RASV-treated mice. Thus, i.t. injection of RASV may offer a novel anti-cancer approach by eliciting transformation of immunosuppressive MDSCs into TNF-α-secreting neutrophils and reducing the generation of Treg cells, especially in the presence of tumor-specific CTLs. Collectively, these data will provide us an insight for the development of new anti-tumor approaches to overcome the immunosuppressive environment generated by tumors.
减毒沙门氏菌疫苗显示出治疗癌症的效果,但潜在机制尚未得到很好的研究。在本研究中,肿瘤内(i.t.)注射重组减毒鼠伤寒沙门氏菌疫苗(RASV)显著抑制了 Her-2/neu 表达的肿瘤生长。尽管在 RASV 治疗的小鼠中耗尽 CD8+细胞显著恢复了肿瘤生长,但 Her-2/neu 特异性细胞毒性 T 淋巴细胞(CTL)的诱导与抗肿瘤效应的产生并没有很好的相关性。因此,我们假设 RASV 可能诱导肿瘤微环境从免疫抑制到免疫原性的转变,以减少抑制力,最终引发成功的抗肿瘤反应。我们发现,肿瘤内注射 RASV 显著增加了 CD11b+Gr-1+髓样细胞的水平,这些细胞被鉴定为髓系来源的抑制细胞(MDSC),但其中很大一部分细胞是 TNF-α 分泌的 Ly6-G(高)亚群,它们可以作为抗肿瘤效应细胞发挥作用。我们进一步研究了 RASV 是否可以调节免疫抑制性 Treg 细胞,结果发现 RASV 治疗的小鼠中 CD4+CD25+Foxp3+Treg 细胞显著减少。因此,肿瘤内注射 RASV 可能通过将免疫抑制性 MDSC 转化为 TNF-α 分泌的中性粒细胞并减少 Treg 细胞的产生来提供一种新的抗肿瘤方法,特别是在存在肿瘤特异性 CTL 的情况下。总之,这些数据将为我们开发新的抗肿瘤方法提供启示,以克服肿瘤产生的免疫抑制环境。