4.8 Article

Directing cell therapy to anatomic target sites in vivo with magnetic resonance targeting

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NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms9009

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资金

  1. Medical Research Council (MRC), UK [G0902317/1]
  2. CR-UK [C11712/A13028]
  3. Medical Research Council [MR/J013110/1]
  4. King's College London and UCL Comprehensive Cancer Imaging Centre CR-UK EPSRC
  5. MRC (England)
  6. National Centre for the Replacement, Reduction and Refinement of Animal in Research (NC3Rs)
  7. UK Regenerative Medicine Platform Safety Hub (MRC) [MR/K026739/1]
  8. Eli Lilly and Company
  9. DoH (England)
  10. Cancer Research UK [13028] Funding Source: researchfish
  11. Engineering and Physical Sciences Research Council [EP/I014667/1] Funding Source: researchfish
  12. Medical Research Council [MR/K026739/1, G0902317] Funding Source: researchfish
  13. EPSRC [EP/I014667/1] Funding Source: UKRI
  14. MRC [G0902317, MR/K026739/1, MR/M008894/1, MR/J013110/1] Funding Source: UKRI

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Cell-based therapy exploits modified human cells to treat diseases but its targeted application in specific tissues, particularly those lying deep in the body where direct injection is not possible, has been problematic. Here we use a magnetic resonance imaging (MRI) system to direct macrophages carrying an oncolytic virus, Seprehvir, into primary and metastatic tumour sites in mice. To achieve this, we magnetically label macrophages with super-paramagnetic iron oxide nanoparticles and apply pulsed magnetic field gradients in the direction of the tumour sites. Magnetic resonance targeting guides macrophages from the bloodstream into tumours, resulting in increased tumour macrophage infiltration and reduction in tumour burden and metastasis. Our study indicates that clinical MRI scanners can not only track the location of magnetically labelled cells but also have the potential to steer them into one or more target tissues.

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