| Literature DB >> 26573799 |
Richard Tavaré1, Helena Escuin-Ordinas2, Stephen Mok3, Melissa N McCracken3, Kirstin A Zettlitz4, Felix B Salazar4, Owen N Witte5, Antoni Ribas6, Anna M Wu7.
Abstract
The rapidly advancing field of cancer immunotherapy is currently limited by the scarcity of noninvasive and quantitative technologies capable of monitoring the presence and abundance of CD8(+) T cells and other immune cell subsets. In this study, we describe the generation of (89)Zr-desferrioxamine-labeled anti-CD8 cys-diabody ((89)Zr-malDFO-169 cDb) for noninvasive immuno-PET tracking of endogenous CD8(+) T cells. We demonstrate that anti-CD8 immuno-PET is a sensitive tool for detecting changes in systemic and tumor-infiltrating CD8 expression in preclinical syngeneic tumor immunotherapy models including antigen-specific adoptive T-cell transfer, agonistic antibody therapy (anti-CD137/4-1BB), and checkpoint blockade antibody therapy (anti-PD-L1). The ability of anti-CD8 immuno-PET to provide whole body information regarding therapy-induced alterations of this dynamic T-cell population provides new opportunities to evaluate antitumor immune responses of immunotherapies currently being evaluated in the clinic. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26573799 PMCID: PMC4703530 DOI: 10.1158/0008-5472.CAN-15-1707
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701