Université Paris-Saclay, CEA, DMTS, SPI, 91191, Gif-Sur-Yvette, France.
Université Paris-Saclay, CEA, CNRS, Inserm, BioMaps, 91401, Orsay, France.
Eur J Nucl Med Mol Imaging. 2023 Sep;50(11):3192-3201. doi: 10.1007/s00259-023-06268-3. Epub 2023 Jun 7.
The resistance of glioblastoma stem cells (GSCs) to treatment is one of the causes of glioblastoma (GBM) recurrence. Endothelin A receptor (ET) overexpression in GSCs constitutes an attractive biomarker for targeting this cell subpopulation, as illustrated by several clinical trials evaluating the therapeutic efficacy of endothelin receptor antagonists against GBM. In this context, we have designed an immunoPET radioligand combining the chimeric antibody targeting ET, chimeric-Rendomab A63 (xiRA63), with Zr isotope and evaluated the abilities of xiRA63 and its Fab (ThioFab-xiRA63) to detect ET tumors in a mouse model xenografted orthotopically with patient-derived Gli7 GSCs.
Radioligands were intravenously injected and imaged over time by µPET-CT imaging. Tissue biodistribution and pharmacokinetic parameters were analyzed, highlighting the ability of [Zr]Zr-xiRA63 to pass across the brain tumor barrier and achieve better tumor uptake than [Zr]Zr-ThioFab-xiRA63.
This study shows the high potential of [Zr]Zr-xiRA63 in specifically targeting ET tumors, thus raising the possibility of detecting and treating ET GSCs, which could improve the management of GBM patients.
神经胶质瘤干细胞(GSCs)对治疗的耐药性是神经胶质瘤(GBM)复发的原因之一。GSCs 中内皮素 A 受体(ET)的过表达构成了靶向该细胞亚群的有吸引力的生物标志物,这已被几项临床试验所证明,这些临床试验评估了内皮素受体拮抗剂对 GBM 的治疗效果。在这种情况下,我们设计了一种免疫 PET 放射性配体,将靶向 ET 的嵌合抗体、嵌合型-Rendomab A63(xiRA63)与 Zr 同位素结合,并评估了 xiRA63 及其 Fab(ThioFab-xiRA63)在原位移植患者来源的 Gli7 GSCs 的小鼠模型中检测 ET 肿瘤的能力。
放射性配体通过静脉注射,并通过 µPET-CT 成像随时间进行成像。分析了组织分布和药代动力学参数,突出了 [Zr]Zr-xiRA63 穿过脑肿瘤屏障的能力,并实现了比 [Zr]Zr-ThioFab-xiRA63 更好的肿瘤摄取。
这项研究表明 [Zr]Zr-xiRA63 具有特异性靶向 ET 肿瘤的巨大潜力,从而有可能检测和治疗 ET GSCs,这可能改善 GBM 患者的治疗管理。