IRBMP Angeletti, Via Pontina km 30,600, 00040 Pomezia, Italy.
Vaccine. 2010 Apr 30;28(20):3522-30. doi: 10.1016/j.vaccine.2010.03.020. Epub 2010 Mar 21.
The telomerase reverse transcriptase (TERT) is an attractive target for cancer vaccination because its expression is reactivated in most tumors. In this study, we have evaluated the ability of a genetic vaccine targeting murine TERT (mTERT) based on DNA electroporation (DNA-EP) and adenovirus serotype 6 (Ad6) to exert therapeutic effects in combination with a novel TLR9 agonist, referred to as immune modulatory oligonucleotide (IMO), as an adjuvant. IMO was administered to mice at the same time as vaccine. IMO induced dose-dependent cytokine secretion and activation of NK cells. Most importantly, vaccination of mice with IMO in combination with mTERT vaccine conferred therapeutic benefit in tumor bearing animals and this effect was associated with increased NK, DC and T cell tumor infiltration. These data show that appropriate combination of a DNA-EP/Ad6-based cancer vaccine against TERT with IMO induces multiple effects on innate and adaptive immune responses resulting in a significant antitumor efficacy.
端粒酶逆转录酶(TERT)是癌症疫苗接种的一个有吸引力的靶点,因为它的表达在大多数肿瘤中被重新激活。在这项研究中,我们评估了一种基于 DNA 电穿孔(DNA-EP)和腺病毒血清型 6(Ad6)的靶向小鼠 TERT(mTERT)的基因疫苗与新型 TLR9 激动剂(称为免疫调节寡核苷酸(IMO))联合作为佐剂的治疗效果。IMO 在给予疫苗的同时给予小鼠。IMO 诱导剂量依赖性细胞因子分泌和 NK 细胞激活。最重要的是,用 IMO 联合 mTERT 疫苗接种肿瘤荷瘤动物可赋予治疗益处,这种效果与 NK、DC 和 T 细胞肿瘤浸润增加有关。这些数据表明,适当的 DNA-EP/Ad6 基于 TERT 的癌症疫苗与 IMO 的组合诱导对先天和适应性免疫反应的多种影响,从而导致显著的抗肿瘤功效。