Cell-Based Tracers as Trojan Horses for Image-Guided Surgery

Surgeons rely almost completely on their own vision and palpation to recognize affected tissues during surgery. Consequently, they are often unable to distinguish between different cells and tissue types. This makes accurate and complete resection cumbersome. Targeted image-guided surgery (IGS) prov...

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Bibliographic Details
Published inInternational journal of molecular sciences Vol. 22; no. 2; p. 755
Main Authors Sier, Vincent Q, de Vries, Margreet R, van der Vorst, Joost R, Vahrmeijer, Alexander L, van Kooten, Cornelis, Cruz, Luis J, de Geus-Oei, Lioe-Fee, Ferreira, Valerie, Sier, Cornelis F M, Alves, Frauke, Muthana, Munitta
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 13.01.2021
MDPI
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Summary:Surgeons rely almost completely on their own vision and palpation to recognize affected tissues during surgery. Consequently, they are often unable to distinguish between different cells and tissue types. This makes accurate and complete resection cumbersome. Targeted image-guided surgery (IGS) provides a solution by enabling real-time tissue recognition. Most current targeting agents (tracers) consist of antibodies or peptides equipped with a radiolabel for Positron Emission Tomography (PET) and Single Photon Emission Computed Tomography (SPECT), magnetic resonance imaging (MRI) labels, or a near-infrared fluorescent (NIRF) dye. These tracers are preoperatively administered to patients, home in on targeted cells or tissues, and are visualized in the operating room via dedicated imaging systems. Instead of using these 'passive' tracers, there are other, more 'active' approaches of probe delivery conceivable by using living cells (macrophages/monocytes, neutrophils, T cells, mesenchymal stromal cells), cell(-derived) fragments (platelets, extracellular vesicles (exosomes)), and microorganisms (bacteria, viruses) or, alternatively, 'humanized' nanoparticles. Compared with current tracers, these active contrast agents might be more efficient for the specific targeting of tumors or other pathological tissues (e.g., atherosclerotic plaques). This review provides an overview of the arsenal of possibilities applicable for the concept of cell-based tracers for IGS.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms22020755