免疫疗法
癌症研究
免疫系统
T细胞
医学
癌症免疫疗法
癌症
免疫学
接种疫苗
CpG寡核苷酸
生物
内科学
生物化学
基因
基因表达
DNA甲基化
作者
Israt S. Alam,Aaron T. Mayer,Idit Sagiv-Barfi,Kezheng Wang,Ophir Vermesh,Debra K. Czerwinski,Emily M. Johnson,Michelle L. James,Ronald Levy,Sanjiv S. Gambhir
摘要
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.
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