期刊
INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 14, 期 -, 页码 8421-8432出版社
DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S218488
关键词
magnetic targeting; biocompatibility; immunoaffinity chromatography; cold tumor; T cell
资金
- Emerging Fields Initiative BIG-THERA of the Friedrich-Alexander-Universitat Erlangen-Nurnberg (FAU)
- Deutsche Forschungsgemeinschaft [AL 552/5-3, SPP1681]
- Forschungsstiftung Medizin am Universitatsklinikum Erlangen
- Manfred-Roth-Stiftung, Furth, Germany
- FAU
- Deutsche Forschungsgemeinschaft
Purpose. Immune activation with T cell tumor infiltration is beneficial for the prognosis of patients suffering from solid cancer. Depending on their immune status, solid tumors can be immunologically classified into three groups: hot tumors are infiltrated with T lymphocytes, cold tumors are not infiltrated and immune excluded tumors are only infiltrated in the peripheral tumor tissue. Checkpoint inhibitors provide new therapeutic options for hot tumors by triggering the immune response of T cells. In order to enable this for cold tumors as well, T cells must be enriched in the tumor. Therefore, we use the principle of magnetic targeting to guide T cells loaded with citrate-coated superparamagnetic iron oxide nanopartides (SPIONcitrate) to the tumor by an externally applied magnetic field. Methods: SPIONcitrate were produced by alkaline coprecipitation of iron(II) and iron(III) chloride and in situ coating with sodium citrate. The concentration-dependent cytocompatibility of the particles was determined by flow cytometry and blood stability assays. Atomic emission spectroscopy was used for the quantification of the particle uptake into T lymphocytes. The attractability of the loaded cells was observed by live-cell imaging in the presence of an externally applied magnetic field. Results: SPIONcitrate displayed good cytocompatibility to T cells and did not show any sign of aggregation in blood. Finally, SPIONcitrate-loaded T cells were strongly attracted by a small external magnet. Conclusion: T cells can be magnetized by incorporation of SPIONcitrate for magnetic targeting. The production of the particle-cell hybrid system is straightforward, as the loading process only requires basic laboratory devices and the loading efficiency is sufficient for cells being magnetically controllable. For these reasons, SPIONcitrate are potential suitable candidates for magnetic T cell targeting.
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