Abstract
Purpose
Although cellular immunotherapy is expected as a new cancer treatment, its therapeutic efficiency is limited in solid tumors, because most cells return to the bloodstream rather than adhere to the target site. Therefore, we are motivated to develop a technique to concentrate the cells in the blood flow using active control of bubble-surrounded cells under ultrasound exposure considering both aspects of cell controllability and viability.
Methods
We prepared a lipid bubble conjugating ligand to adhere to the surface of the T-cells. First, we evaluated the cell controllability by retaining the cells on a wall of an artificial blood vessel through continuous ultrasound exposure. Next, we investigated the cell viability under ultrasound exposure in a suspension with various bubble concentrations.
Results
We estimated the concentration of bubbles when the adhesion to the cell surface was saturated. Then, we evaluated the cell viability with various conditions of ultrasound exposure and bubble concentrations. However, it was confirmed that cell damage occurred under conditions that achieved proper control of the cells. Therefore, we exposed the cells to burst waves to reduce the applied ultrasound intensity. Consequently, the significant increase in cell viability was confirmed to be inversely proportional to the duty ratio.
Conclusion
To retain cells on a vessel wall, determining the appropriate ultrasound condition including sound pressure and waveform is important to maintain cell viability.
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Data availability
The authors confirm that the data supporting the findings of this study are available within the article.
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Acknowledgements
This research was supported by a grant from the Japan Society for the Promotion of Science (JSPS) through KAKENHI Grant No. 20H04547, and the Uehara Memorial Foundation.
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Kajita, N., Ito, Y., Watanabe, S. et al. Viability variation of T-cells under ultrasound exposure according to adhesion condition with bubbles. J Med Ultrasonics 50, 121–129 (2023). https://doi.org/10.1007/s10396-022-01277-5
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DOI: https://doi.org/10.1007/s10396-022-01277-5