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Flow Cytometric Immunophenotyping: Minimal Differences in Fresh and Cryopreserved Peripheral Blood Mononuclear Cells
Andrea Tompa1,2, Junko Johansson2, Ulrika Islander2,3
1Department of Clinical Diagnostics, School of Health and Welfare, Jönköping University, SE-551 11 Jönköping, Sweden.
Insights
Cryopreservation minimally impacts flow cytometry immunophenotyping of peripheral blood mononuclear cells (PBMCs). Results suggest cryostorage is feasible, but whole blood comparisons require careful consideration for accurate immunological monitoring.
Area of Science:
- Immunology
- Cell Biology
- Biotechnology
Background:
- Flow cytometry is crucial for immunophenotyping in disease monitoring.
- Investigating the impact of sample processing on cell subpopulations is vital for reliable results.
Purpose of the Study:
- To evaluate the effects of isolation and cryopreservation on various immune cell subsets using flow cytometry.
- To compare fresh whole blood with isolated and cryopreserved peripheral blood mononuclear cells (PBMCs).
Main Methods:
- Peripheral blood from healthy donors was collected.
- Cells were prepared for flow cytometric analysis using standardized antibody panels.
- Comparisons were made between fresh PBMCs, cryopreserved PBMCs, and fresh whole blood.
Main Results:
- No significant differences were observed in CD4+ T helper (Th), T regulatory (Treg), CD8+ T cytotoxic (Tc), CD56+ NK, CD19+ B cells, or monocyte percentages between fresh and cryopreserved PBMCs.
- Whole blood showed distinct differences in cell percentages compared to both fresh and cryopreserved PBMCs, with lower Th and NK cells but higher Tregs, Tc, and B cells.
Conclusions:
- Flow cytometric immunophenotyping of PBMCs shows minimal variation after cryopreservation, supporting cryostorage for future analysis.
- Direct comparison of results between whole blood and isolated/cryopreserved PBMCs should be done cautiously.
- Findings aid in standardizing flow cytometry protocols for clinical and research applications.
Abstract:
Background/Objectives: Flow cytometry is a convenient tool in immunophenotyping for monitoring the status of immunological conditions and diseases. The aim of this study was to investigate the effect of isolation and cryopreservation by flow cytometric analysis on subpopulations of CD4+ T helper (Th), T regulatory (Treg), CD8+ T cytotoxic (Tc), CD56+ NK, CD19+ B and monocytes. Freshly isolated and cryopreserved peripheral blood mononuclear cells (PBMCs) were compared to fresh whole blood. Methods: Peripheral blood was collected from healthy donors and prepared for flow cytometric analysis using the same panels of antibodies throughout the study. Results: Comparisons between fresh (F)- and cryopreserved (C)-PBMCs showed no major differences in percentages of CD4+, Th1, Th2 and CD4+CD25+CD127low Treg cells. No differences in percentage of CD8+ or subpopulations of naive/stem, central or effector memory cells were observed between F- and C-PBMCs. The percentage of CD56+ NK cells, CD19+ B cells or classical and nonclassical monocytes did not differ between F-and C-PBMCs either. On the contrary, whole blood had lower percentages of Th and NK cells but higher percentages of Th1, Th17, Th1Th17, Tregs, Tc and B cells compared to C-PBMCs, while it had a higher proportion of Tc compared to F-PBMCs. Conclusions: Flow cytometric immunophenotyping minimally differs between freshly isolated and cryopreserved PBMCs. This implies the possibility of cryostorage of cohorts for later analysis. Importantly, care must be taken when comparing results from whole blood with isolated and cryopreserved PBMCs. Collectively, these results can contribute to the standardization of flow cytometric protocols in both clinical and research settings.
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