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Updated: Feb 5, 2026

Multicolor Flow Cytometry Analyses of Cellular Immune Response in Rhesus Macaques
Published on: April 22, 2010
Deep phenotyping of immune cell populations by optimized and standardized flow cytometry analyses
Fabien Pitoiset1,2, Lydie Cassard3, Karim El Soufi1,2
1Sorbonne Universités, UPMC Univ Paris 06, INSERM, UMR S 959, Immunology-Immunopathology- Immunotherapy (I3), F-75005, Paris, France.
Insights
Researchers developed 12 optimized 10-color flow cytometry panels for deep immune cell phenotyping from whole blood. These panels aid in monitoring autoimmune and cancer patients, identifying rare cells, and discovering new biomarkers.
Area of Science:
- Immunology
- Clinical Trials
- Biomarker Discovery
Background:
- Multicolor flow cytometry is crucial for immune cell phenotyping in clinical trials.
- Defining antibody combinations for detailed immune cell subset analysis, especially rare populations, remains challenging.
Purpose of the Study:
- To develop and validate 10-color flow cytometry panels for deep immunophenotyping of whole blood immune cells.
- To facilitate patient monitoring in autoimmune and cancer clinical trials.
Main Methods:
- Development and validation of 12 distinct 10-color flow cytometry panels.
- Application to whole blood samples for comprehensive immune cell analysis.
- Drying of most panels for improved standardization.
Main Results:
- Enabled advanced analysis of major immune cell subsets including T cells, B cells, NK cells, MAIT cells, myeloid cells, monocytes, and dendritic cells.
- Demonstrated feasibility using less than 2 ml of whole blood.
- Panels allow for the identification of rare immune cell populations.
Conclusions:
- These optimized flow cytometry panels provide a powerful tool for deep immunophenotyping.
- They are valuable for monitoring immune cells in autoimmune and cancer patients.
- The panels may lead to the discovery of novel biomarkers and therapeutic targets.
Abstract:
Multicolor flow cytometry is a technology of choice for phenotyping of immune cells, and it can be used routinely for the follow up of patients in clinical trials. But it is challenging to define combinations of conjugated antibodies that efficiently allow the detailed analysis of major immune cell subsets and the identification of rare cell populations. In a collaborative work among the Immunology, Immunopathology, Immunotherapy (I3 ) laboratory, and the laboratory of immunomonitoring in oncology (L.I.O), we developed and validated 12 different 10-color flow cytometry panels that allow the deep immunophenotyping of cells from whole blood for the follow up of autoimmune and cancer patients. Here, we describe these optimized flow cytometry panels, showing that they provide the advanced analysis of T cells (including regulatory T cells), B cells, NK cells, MAIT cells, myeloid cells, monocytes, and dendritic cells. Most of the panels have been dried to improve standardization of the labeling and the entire procedure can be performed on less than 2 ml of whole blood. These deep immunophenotyping flow cytometry panels constitute a powerful tool for the monitoring of immune blood cells and will hopefully lead to the discovery of new biomarkers and potential therapeutic targets in autoimmune and cancer clinical trials. © 2018 International Society for Advancement of Cytometry.
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