研究目的
To investigate how route of administration, cell type and host immune status affect the fate of administered cells in the context of cell-based regenerative medicine therapies.
研究成果
The non-invasive imaging platform can expose the general organ distribution of cell therapies and their tumourigenic potential. The intra-arterial route may be more hazardous than intravenous administration for certain cell types. Clinically tested human umbilical cord-derived MSCs can transiently and unexpectedly proliferate when administered intravenously to mice, suggesting that therapies with these cells should proceed with caution.
研究不足
The study is limited to preclinical models, and the findings may not directly translate to clinical settings. The use of immunocompromised mice may not fully represent the human immune response. The study focuses on short-term effects, and long-term safety and efficacy remain to be investigated.
1:Experimental Design and Method Selection:
A multi-modal imaging approach combining bioluminescence, optoacoustic, and magnetic resonance imaging was used to assess the safety of different human and murine cell types by following their biodistribution and persistence in mice following administration into the venous or arterial system.
2:Sample Selection and Data Sources:
Human and murine cells, including mesenchymal stem/stromal cells (MSCs), kidney-derived cells, and macrophages, were used.
3:List of Experimental Equipment and Materials:
Bioluminescence imager (IVIS Spectrum, Perkin Elmer), multispectral optoacoustic tomography (MSOT) imaging system (inVision 256-TF, iThera Medical), magnetic resonance imaging (MRI) system (Bruker Avance III spectrometer interfaced to a
4:4 T magnet system). Experimental Procedures and Operational Workflow:
Cells were administered via intravenous (IV) or intracardiac (IC) injection, and their biodistribution and persistence were monitored over time using the aforementioned imaging modalities.
5:Data Analysis Methods:
Bioluminescence signals were quantified by drawing regions of interest (ROIs) from which the total flux was obtained. Statistical analyses were performed using Minitab 17 statistical software.
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