| Literature DB >> 29596062 |
Israt S Alam1,2, Aaron T Mayer1,2,3, Idit Sagiv-Barfi4, Kezheng Wang1,5, Ophir Vermesh1,2, Debra K Czerwinski4, Emily M Johnson1,2,6, Michelle L James1,2,6, Ronald Levy4, Sanjiv S Gambhir1,2.
Abstract
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.Entities:
Keywords: Cancer immunotherapy; Immunology; Oncology; T cells
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Year: 2018 PMID: 29596062 PMCID: PMC5983309 DOI: 10.1172/JCI98509
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808