Department of Radiology.
Molecular Imaging Program at Stanford.
J Clin Invest. 2018 Jun 1;128(6):2569-2580. doi: 10.1172/JCI98509. Epub 2018 May 14.
In situ cancer vaccines are under active clinical investigation, given their reported ability to eradicate both local and disseminated malignancies. Intratumoral vaccine administration is thought to activate a T cell-mediated immune response, which begins in the treated tumor and cascades systemically. In this study, we describe a PET tracer (64Cu-DOTA-AbOX40) that enabled noninvasive and longitudinal imaging of OX40, a cell-surface marker of T cell activation. We report the spatiotemporal dynamics of T cell activation following in situ vaccination with CpG oligodeoxynucleotide in a dual tumor-bearing mouse model. We demonstrate that OX40 imaging was able to predict tumor responses on day 9 after treatment on the basis of tumor tracer uptake on day 2, with greater accuracy than both anatomical and blood-based measurements. These studies provide key insights into global T cell activation following local CpG treatment and indicate that 64Cu-DOTA-AbOX40 is a promising candidate for monitoring clinical cancer immunotherapy strategies.
原位癌症疫苗正在进行积极的临床研究,因为它们据称能够消除局部和播散性恶性肿瘤。瘤内疫苗给药被认为可以激活 T 细胞介导的免疫反应,该反应始于治疗的肿瘤,并在系统中级联。在这项研究中,我们描述了一种 PET 示踪剂(64Cu-DOTA-AbOX40),它能够对 T 细胞激活的细胞表面标志物 OX40 进行非侵入性和纵向成像。我们报告了在双肿瘤荷瘤小鼠模型中,用 CpG 寡脱氧核苷酸进行原位疫苗接种后 T 细胞激活的时空动力学。我们证明,基于第 2 天的肿瘤示踪剂摄取,OX40 成像能够在治疗后第 9 天预测肿瘤反应,其准确性高于解剖学和基于血液的测量。这些研究为局部 CpG 治疗后全身 T 细胞激活提供了重要的见解,并表明 64Cu-DOTA-AbOX40 是监测临床癌症免疫治疗策略的有前途的候选物。