Cross-platform immunophenotyping of human peripheral blood mononuclear cells with four high-dimensional flow cytometry panels
- PMID: 36571245
- DOI: 10.1002/cyto.a.24715
Cross-platform immunophenotyping of human peripheral blood mononuclear cells with four high-dimensional flow cytometry panels
Abstract
Immunophenotyping using high dimensional flow cytometry is a central component of human immune system multi-omic studies. We present four high parameter flow cytometry panels for deep immunophenotyping of human peripheral blood mononuclear cells (PBMC). This set of four 25+ color panels include 64 cell surface markers to resolve broad immune compartment populations, as well as activation and memory of specific T, B, natural killer (NK), and myeloid lineages. Common lineage bridging markers are integrated into each panel to allow for inter-panel quality control through major lineage frequency verification. These panels were developed using a five laser BD Symphony A5 conventional cytometer and successfully transferred to a five laser Cytek Aurora spectral cytometer capable of acquiring the panels. Nine representative PBMC samples were stained with the four phenotyping panels and acquired on both instruments to evaluate population frequency and visual staining patterns for gating between the systems. Both instruments produced comparable high quality flow cytometry data and supported our decision to acquire samples on the spectral cytometer moving forward. This modular set of panels and instrument performance metrics provide guidelines for designing flow cytometry experiments suitable for longitudinal or cross-sectional immune profiling.
Keywords: conventional cytometry; high dimensional flow cytometry; immunophenotyping; peripheral blood mononuclear cells (PBMC); spectral cytometry.
© 2022 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry.
References
REFERENCES
-
- Chu X, Zhang B, Koeken VACM, Gupta MK, Li Y. Multi-omics approaches in immunological research. Front Immunol. 2021;12:668045.
-
- Maecker HT, McCoy JP, Nussenblatt R. Standardizing immunophenotyping for the human immunology project. Nat Rev Immunol. 2012;12:191-200.
-
- Chattopadhyay PK, Roederer M. A mine is a terrible thing to waste: high content, single cell technologies for comprehensive immune analysis. Am J Transplant. 2015;15:1155-61.
-
- Pitoiset F, Cassard L, El Soufi K, Boselli L, Grivel J, Roux A, et al. Deep phenotyping of immune cell populations by optimized and standardized flow cytometry analyses. Cytometry A. 2018;93:793-802.
-
- Verschoor CP, Kohli V. Cryopreserved whole blood for the quantification of monocyte, T-cell and NK-cell subsets, and monocyte receptor expression by multi-color flow cytometry: a methodological study based on participants from the Canadian longitudinal study on aging. Cytometry A. 2018;93:548-55.
MeSH terms
LinkOut - more resources
Full Text Sources