Centro de Investigaciones Oncológicas-Fundación Cáncer, Buenos Aires, Argentina.
Grupo de Bioestadística Aplicada, Departamento de Ecología, Genética y Evolución, Instituto de Ecología, Genética y Evolución de Buenos Aires (IEGEBA-UBA/CONICET), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
Front Immunol. 2018 Nov 2;9:2531. doi: 10.3389/fimmu.2018.02531. eCollection 2018.
As cutaneous melanoma (CM) currently remains with a bleak prognosis, thorough investigation of new treatment options are of utmost relevance. In the phase II/III randomized clinical trial (CASVAC-0401), the repeated immunization of stages IIB-III CM patients with the irradiated, allogeneic cellular CSF-470 vaccine plus the adjuvants bacillus Calmette-Guerin (BCG) and recombinant human granulocyte macrophage colony-stimulating factor (rhGM-CSF) demonstrated a significant benefit over IFN-alpha2B treatment in distant metastasis-free survival. Here we present on the short and long term immune monitoring results after completing the 2-year protocol; a continuation of the previous report by Mordoh et al. (1). We demonstrate that the repeated CSF-470 vaccinations stimulated a long term cellular and humoral immunity response directed against the vaccine antigens. In the case of 2 patients, we are able to show that a similar immune response was generated against autologous antigens. Evaluation of inhibitory receptor co-expression on patient's T cells indicates that the vaccination protocol did not stimulate T cell exhaustion. In order to better understand the basis for the efficacious vaccine responses observed, we investigated the short term immune events following vaccine injection. A significant increase in C-reactive protein (CRP) and IL-6 was observed 24 h after vaccination, with studies suggesting IL-6 production occurs in the vaccine site. We demonstrate that CRP enhances the cytotoxicity of peripheral blood mononuclear cells (PBMC) against melanoma cells in an model. Additionally, CRP stimulates the release of pro and anti-inflammatory cytokines from PBMC. As our results demonstrate that successive vaccinations with CSF-470 plus adjuvants promoted an increase in both anti-tumor innate and adaptive immunity, we propose a subsequent model of action.
由于皮肤黑色素瘤(CM)目前的预后仍然不容乐观,因此深入研究新的治疗方案至关重要。在 II/III 期随机临床试验(CASVAC-0401)中,对 IIB-III 期 CM 患者重复使用照射后的同种异体 CSF-470 疫苗加佐剂卡介苗(BCG)和重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)进行免疫接种,与 IFN-α2B 治疗相比,在无远处转移存活方面表现出显著益处。在这里,我们展示了完成 2 年方案后的短期和长期免疫监测结果;这是 Mordoh 等人之前报告的延续。我们证明,重复 CSF-470 疫苗接种可刺激针对疫苗抗原的长期细胞和体液免疫应答。在 2 名患者的情况下,我们能够证明针对自身抗原产生了类似的免疫应答。对患者 T 细胞抑制性受体共表达的评估表明,疫苗接种方案并未刺激 T 细胞耗竭。为了更好地理解观察到的有效疫苗反应的基础,我们研究了疫苗接种后短期的免疫事件。接种疫苗后 24 小时观察到 C 反应蛋白(CRP)和 IL-6 的显著增加,有研究表明 IL-6 的产生发生在疫苗部位。我们证明 CRP 增强了外周血单核细胞(PBMC)对黑素瘤细胞的细胞毒性,这在 模型中得到了证实。此外,CRP 刺激 PBMC 释放促炎和抗炎细胞因子。由于我们的结果表明 CSF-470 加佐剂的连续接种可促进抗肿瘤先天和适应性免疫的增加,因此我们提出了后续的作用模型。