A novel probe for the non-invasive detection of tumor-associated inflammation
Volume 2, Issue 2
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eLocation ID: e23034http://dx.doi.org/10.4161/onci.23034
F MRI, imaging, inflammation, myeloid-derived suppressor cells, near infrared probe, tumor, tumor-infiltrating leukocytes
Authors: Anthony Balducci, Yi Wen, Yang Zhang, Brooke M. Helfer, T. Kevin Hitchens, Wilson S. Meng, Amy K. Wesa and Jelena M. Janjic View affiliations
A novel dual-mode contrast agent was formulated through the addition of an optical near infrared (NIR) probe to a perfluorocarbon (PFC)-based 19F magnetic resonance imaging (MRI) agent, which labels inflammatory cells in situ. A single PFC-NIR imaging agent enables both a qualitative, rapid optical monitoring of an inflammatory state and a quantitative, detailed and tissue-depth independent magnetic resonance imaging (MRI). The feasibility of in vivo optical imaging of the inflammatory response was demonstrated in a subcutaneous murine breast carcinoma model. Ex vivo optical imaging was used to quantify the PFC-NIR signal in the tumor and organs, and results correlated well with quantitative 19F NMR analyses of intact tissues. 19F MRI was employed to construct a three-dimensional image of the cellular microenvironment at the tumor site. Flow cytometry of isolated tumor cells was used to identify the cellular localization of the PFC-NIR probe within the tumor microenvironment. Contrast is achieved through the labeling of host cells involved in the immune response, but not tumor cells. The major cellular reservoir of the imaging agent were tumor-infiltrating CD11b+ F4/80low Gr-1low cells, a cell subset sharing immunophenotypic features with myeloid-derived suppressor cells (MDSCs). These cells are recruited to sites of inflammation and are implicated in immune evasion and tumor progression. This PFC-NIR contrast agent coupled to non-invasive, quantitative imaging techniques could serve as a valuable tool for evaluating novel anticancer agents.
Received: September 28, 2012; Accepted: November 28, 2012; Published Online: February 1, 2013