Scientific reports · 2026
Expanding the supply of human leukocytes for research by harvesting cell concentrates from Trima Accel tubing sets.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Kronenberg Katharina, Glehr Gunther, Haehnel Viola, Dormann Frauke, Pamler Irene, Preverin Giulia, Arella Fabiola, Kapinsky Michael, Riquelme Paloma, Offner Robert, Schlitt Hans J, Beckhove Philipp, Geissler Edward K, Burkhardt Ralph, Hutchinson James A, Brosig Andreas
Аннотация
Leukoreduction system (LRS) chambers from the Trima Accel apheresis platform are widely used as a convenient source of human peripheral blood mononuclear cells (PBMCs) for immunological research. However, increasing demand has prompted the search for alternative sources. Here, we investigated whether residual cell concentrates recovered from Trima Accel tubing sets, typically discarded after platelet apheresis, could serve as a substitute for concentrates obtained from LRS chambers. Paired samples from 20 healthy platelet donors were analyzed for recovered volume, cellular composition and yield, leukocyte subset distribution, and functional responsiveness. Tubing sets contained significantly greater volumes (23.04 ± 14.1 ml vs. 8.14 ± 0.97 ml) but lower leukocyte concentrations (35.19 ± 16.99 × 10³/µl vs. 147.60 ± 59.63 × 10³/µl) than LRS chambers. Absolute leukocyte numbers were slightly higher in LRS chambers. However, cell frequencies in tubing sets showed a minor enrichment of monocytes and a modest lymphocyte depletion. Detailed flow cytometry characterization further revealed comparable distributions of major leukocyte populations and T cell subsets, including naïve and memory compartments, without biologically meaningful differences in activation or differentiation markers. Importantly, PBMCs from both sources exhibited comparable functional responses following phytohemagglutinin (PHA) stimulation, including similar changes in activation marker expression and cytokine production. Short-term storage of tubing set samples for 24 h at 4 °C did not compromise cell viability. Overall, tubing sets represent a functionally equivalent and practical alternative leukocyte source for research applications.