Maes W, Deroose C, Reumers V, Krylyshkina O, Gijsbers R, Baekelandt V, Ceuppens J, Debyser Z, Van Gool S W
Department of Experimental Medicine, Katholieke Universiteit Leuven, Leuven, Belgium.
J Neurooncol. 2009 Jan;91(2):127-39. doi: 10.1007/s11060-008-9691-5. Epub 2008 Sep 12.
The value of bioluminescence imaging (BLI) for experimental cancer models has become firmly established. We applied BLI to the GL261 glioma model in the context of dendritic cell (DC) immunotherapy. Initial validation revealed robust linear correlations between in vivo, ex vivo and in vitro luciferase activity measurements. Ex vivo BLI demonstrated midline crossing and leakage of tumor cells. Orthotopically challenged mice followed with BLI showed an initial adaptation phase, after which imaging data correlated linearly with stereologically determined tumor dimensions. Transition from healthy to moribund state corresponded with an increasing in vivo flux but the onset of neurological deficit was clearly delayed compared to the onset of in vivo flux increase. BLI was implemented in prophylactic immunotherapy and imaging data were prognostic for therapy outcome. Three distinct response patterns were detected. Our data underscore the feasibility of in vivo BLI in an experimental immunotherapeutic setting in the GL261 glioma model.
生物发光成像(BLI)在实验性癌症模型中的价值已得到确凿证实。我们将BLI应用于树突状细胞(DC)免疫治疗背景下的GL261胶质瘤模型。初步验证显示,体内、体外和离体荧光素酶活性测量之间存在强线性相关性。离体BLI显示肿瘤细胞中线交叉和渗漏。用BLI跟踪原位攻击的小鼠显示出初始适应期,此后成像数据与立体定向确定的肿瘤大小呈线性相关。从健康状态到濒死状态的转变与体内通量增加相对应,但与体内通量增加的起始相比,神经功能缺损的发作明显延迟。BLI被应用于预防性免疫治疗,成像数据对治疗结果具有预后意义。检测到三种不同的反应模式。我们的数据强调了在GL261胶质瘤模型的实验性免疫治疗环境中进行体内BLI的可行性。