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- Open Access
Use of magnetic resonance targeting to steer ov-loaded cell-based therapies to tumor sites in vivo
© Muthana et al. 2015
Published: 4 November 2015
Despite considerable progress in the development of cell-based therapies, targeted delivery to specific tissues - particularly those deep in the body where direct injection is not possible - has been problematic. Here we show that tumour-conditioned macrophages infected with oncolytic HSV Seprehvir display a classic activated (M1) profile characterized by the expression of pro-inflammatory factors such as iNOS, IL-6, IL-8 and tumor necrosis factor-α (TNF-α). Furthermore, the M1 macrophages can be magnetically labeled using super-paramagnetic iron oxide nanoparticles (SPIOs) and then steered from the bloodstream into deep target tissues using pulsed magnetic-field gradients inherent to all magnetic resonance imaging systems (MRI). We have called this approach magnetic resonance targeting (MRT) and have used it to deliver a cell-based oncolytic virotherapy.
SPIO-loaded macrophages, armed with Seprehvir, were administered intravenously to mice bearing orthotopic primary and metastatic (lung) prostate tumors. Mice were positioned in the MRI scanner and pulsed magnetic field gradients were applied for 1 hour, to steer the magnetic cells towards the target site by MRT (MRT). In control conditions mice were exposed to the static magnetic field of the scanner but gradients were not pulsed (No MRT).
MRI steering significantly increased uptake of SPIO-loaded macrophages in primary prostate tumours (MRT: 42.2%±2.5 vs. No MRT: 7.17%±0.8, p=0.0001) and pulmonary metastasis (MRT: 17.7%±4 vs. No MRT:4.4%±2.6, p=0.01) as assessed by magnetic relaxometry and MRI and post-mortem by flow cytometry and histology. Crucially, this increased uptake of magnetic, Seprehvir-armed macrophages led to marked tumour shrinkage and reduced metastatic burden.
Our study demonstrates the potential for clinical MRI scanners not only to image such magnetically labeled cells after their injection into the body, but also to steer non-invasively, therapeutically-loaded cells specifically to one or more tumors within the body.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.