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New microfluidic system provides automated alternative to FicollĀ® for leukocyte isolation

Authors :
Melanie M Scully
Sarah M Mickool
Nicholas D Rivelli
Aleksander J Jonca
Gustavo Arnal
Laura G Culligan
Peng Meng Kou
Kyle C Smith
Source :
The Journal of Immunology. 204:86.32-86.32
Publication Year :
2020
Publisher :
The American Association of Immunologists, 2020.

Abstract

Despite its limitations, Ficoll® has remained the primary method of leukocyte isolation for decades due to a lack of viable alternatives. To address this, MicroMedicine has developed SorterraTM, an automated microfluidic system that enables highly consistent label-free white blood cell separation and concentration. In a comparative study, Sorterra recovered 25% more viable lymphocytes than Ficoll, 88 ± 7% and 69 ± 13%, respectively (n=48). Sorterra retained Sorterra and Ficoll isolates were assessed for B cell and T cell functionality. To assess B cells, the isolates were stimulated with R848 and IL-2 (n=9), and total IgG and IgM secretion were evaluated with ELISpot. Secretion from Sorterra and Ficoll isolates was shown to be equivalent using distribution free resampling analysis. To assess T cell functionality, negatively selected T cells from Sorterra and Ficoll isolates were activated with CD3/28 beads and expanded with IL-2 (n=12). The isolates displayed similar T cell activation (89±4% vs. 88±5% CD25+/CD69+), proliferation, and T cell phenotypes (Tn TCM, TEM, TEFF) at 7 and 10 days post activation. Compared to Ficoll, Sorterra enables rapid, automated isolation of leukocytes, consistently yielding more lymphocytes with negligible RBCs and platelet contamination while maintaining T cell and B cell function. By minimizing operator variability, Sorterra has the potential to transform cell separation by automating an outdated, variable, and labor-intensive process.

Subjects

Subjects :
Immunology
Immunology and Allergy

Details

ISSN :
15506606 and 00221767
Volume :
204
Database :
OpenAIRE
Journal :
The Journal of Immunology
Accession number :
edsair.doi...........b274b16926330c62d83e1e3063cd3fec
Full Text :
https://doi.org/10.4049/jimmunol.204.supp.86.32