Centre for Innovative Cancer Research, Ottawa Hospital Research Institute.
Department of Laboratory Medicine, University of Tabuk, Tabuk, Saudi Arabia.
Cancer Immunol Res. 2017 Mar;5(3):211-221. doi: 10.1158/2326-6066.CIR-16-0162. Epub 2017 Feb 3.
Despite improvements in chemotherapy and radical surgical debulking, peritoneal carcinomatosis (PC) remains among the most common causes of death from abdominal cancers. Immunotherapies have been effective for selected solid malignancies, but their potential in PC has been little explored. Here, we report that intraperitoneal injection of an infected cell vaccine (ICV), consisting of autologous tumor cells infected with an oncolytic Maraba MG1 virus expressing IL12, promotes the migration of activated natural killer (NK) cells to the peritoneal cavity in response to the secretion of IFNγ-induced protein-10 (IP-10) from dendritic cells. The recruitment of cytotoxic, IFNγ-secreting NK cells was associated with reduced tumor burden and improved survival in a colon cancer model of PC. Even in mice with bulky PC (tumors > 8 mm), a complete radiologic response was demonstrated within 8 to14 weeks, associated with 100% long-term survival. The impact of MG1-IL12-ICV upon NK-cell recruitment and function observed in the murine system was recapitulated in human lymphocytes exposed to human tumor cell lines infected with MG1-IL12. These findings suggest that an MG1-IL12-ICV is a promising therapy that could provide benefit to the thousands of patients diagnosed with PC each year. .
尽管化疗和激进的手术去瘤有了改善,但腹膜癌转移(PC)仍然是腹部癌症死亡的最常见原因之一。免疫疗法对某些实体恶性肿瘤有效,但它们在 PC 中的潜力尚未得到充分探索。在这里,我们报告说,腹腔内注射一种感染细胞疫苗(ICV),由自体肿瘤细胞感染表达 IL12 的溶瘤 Maraba MG1 病毒组成,可促进激活的自然杀伤(NK)细胞向腹腔迁移,以响应树突状细胞分泌的 IFNγ 诱导蛋白-10(IP-10)。在 PC 的结肠癌模型中,细胞毒性、IFNγ 分泌 NK 细胞的募集与肿瘤负担减少和生存改善相关。即使在患有大块 PC(肿瘤 > 8 毫米)的小鼠中,也在 8 至 14 周内显示出完全的放射学反应,与 100%的长期生存率相关。在人类淋巴细胞中观察到的 MG1-IL12-ICV 对 NK 细胞募集和功能的影响,在感染了 MG1-IL12 的人类肿瘤细胞系的人类肿瘤细胞系中得到了再现。这些发现表明,MG1-IL12-ICV 是一种很有前途的治疗方法,每年可能为数以千计的 PC 患者带来益处。