Department of Oncology and Pathology, Cancer Centre Karolinska, Karolinska Institutet, Stockholm, Sweden.
Cancer Immunol Immunother. 2012 Jun;61(6):865-79. doi: 10.1007/s00262-011-1149-5. Epub 2011 Nov 16.
We previously demonstrated that autologous dendritic cells that have endocytosed apoptotic bodies of chronic lymphocytic leukemia (CLL) cells (Apo-DC) can stimulate antileukemic T cell responses in vitro. In this phase I study, we vaccinated 15 asymptomatic CLL patients at five time points with Apo-DC administered intradermally either alone (cohort I), or in combination with subcutaneous granulocyte-macrophage-colony-stimulating-factor (GM-CSF) (cohort II) or with GM-CSF and intravenous low-dose cyclophosphamide (cohort III). Aim of the study was to evaluate the safety and immunogenicity of Apo-DC alone or in combination with GM-CSF and low-dose cyclophosphamide in CLL patients. All patients completed the vaccination schedule without dose-limiting toxicity. No objective clinical responses were seen. Vaccine-induced leukemia-specific immune responses were evaluated by IFN-γ ELISpot and proliferation assays over a 52 weeks observation period and immune response criteria were defined. According to these criteria, 10/15 patients were defined as immune responders. The frequency of immune-responding patients was higher in cohorts II (3/5) and III (5/5) than in cohort I (2/5). In order to further characterize the induced immune response, estimation of secreted cytokines and CD107-degranulation assay were performed. Clustering of T and CLL cells was observed in CD107-degranulation assay and visualized by confocal microscopy. Additionally, assessment of regulatory T cells (T(regs)) revealed their significantly lower frequencies in immune responders versus non-responders (P < 0.0001). Cyclophosphamide did not reduce T(regs) frequency. In conclusion, vaccination with Apo-DC + GM-CSF and cyclophosphamide was safe and elicited anti-CLL immune responses that correlated inversely with T(regs) levels. Lack of clinical responses highlights the necessity to develop more potent vaccine strategies in B cell malignancies.
我们之前的研究表明,内吞慢性淋巴细胞白血病(CLL)细胞凋亡小体的自体树突状细胞(Apo-DC)可以在体外刺激抗白血病 T 细胞反应。在这项 I 期研究中,我们在五个时间点用皮内注射的方式给 15 例无症状 CLL 患者接种 Apo-DC,这些患者被分为三组:仅接受 Apo-DC 接种(I 组),或联合皮下粒细胞-巨噬细胞集落刺激因子(GM-CSF)(II 组),或联合 GM-CSF 和静脉注射低剂量环磷酰胺(III 组)。本研究的目的是评估 Apo-DC 单独或联合 GM-CSF 和低剂量环磷酰胺在 CLL 患者中的安全性和免疫原性。所有患者均完成了接种计划,未出现剂量限制毒性。未观察到客观的临床反应。通过 IFN-γ ELISpot 和增殖试验在 52 周的观察期内评估疫苗诱导的白血病特异性免疫反应,并定义免疫反应标准。根据这些标准,15 例患者中有 10 例被定义为免疫反应者。与 I 组(2/5)相比,II 组(3/5)和 III 组(5/5)的免疫反应患者频率更高。为了进一步描述诱导的免疫反应,进行了细胞因子分泌和 CD107 脱颗粒测定。在 CD107 脱颗粒试验中观察到 T 细胞和 CLL 细胞的聚类,并通过共聚焦显微镜进行可视化。此外,评估调节性 T 细胞(Tregs)显示,免疫反应者的 Tregs 频率明显低于无反应者(P<0.0001)。环磷酰胺并未降低 Tregs 频率。总之,用 Apo-DC+GM-CSF 和环磷酰胺进行疫苗接种是安全的,并引起了与 Tregs 水平呈负相关的抗 CLL 免疫反应。缺乏临床反应突出表明需要开发更有效的 B 细胞恶性肿瘤疫苗策略。