bioRxivImmunologyPreprint
High-dimensional spectral cytometry panels for whole blood immune phenotyping
T. Dott, S. Culina, R. Chemali, C. Ait Mansour, F. Dubois, B. Jagla, J. M. Doisne, L. Rogge, F. Huetz, F. Jönsson, P.-H. Commere, J. Di Santo, B. Terrier, L. Quintana-Murci, D. Duffy, M. Hasan, Milieu Interieur Consortium
Abstract
The need to understand the mechanisms and pathways of immune responses in pathogenic conditions such as cancer and autoimmunity requires awareness of natural immune variability in healthy subjects. To this end, various systems immunology studies have been established. Among them, the Milieu Interieur (MI) study was established to define the boundaries of a healthy immune response and identify determinants of immune response variation. MI used immunophenotyping of a 1000 healthy donor cohort by flow cytometry as a principal outcome for immune variance at steady state. For the 10-year longitudinal MI study, we have developed two high-dimensional spectral flow cytometry panels that allow deep characterization of innate and adaptive whole blood immune cells (35 and 34 fluorescent markers, respectively) and standardized the protocol for sample handling, staining, acquisition, and data analysis. This permits the reproducible quantification of over 182 immune cell phenotypes through robust immunophenotyping at a single site. This highly standardized protocol was applied to samples from patients with autoimmune/inflammatory diseases. It is currently used for characterization of the impact of age and environmental factors on peripheral blood immune phenotypes of >400 donors from the initial MI cohort.
- organism: human
- assay: flow cytometry
- research focus: cell type annotation
- research focus: clustering
- research focus: differential expression
- research focus: cell-cell communication
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Beyond 40 fluorescent probes for deep phenotyping of blood mononuclear cells, using spectral technology.
S. Schmutz, P.-H. Commere, … M. Hasan·bioRxiv·Jul 27, 2023
- 50-color phenotyping of the human immune system with in-depth assessment of T cells and dendritic cells
A. J. Konecny, P. Mage, … F. Mair·bioRxiv·Dec 14, 2023
- 45-Color Full Spectrum Flow Cytometry Panel for Deep Immunophenotyping of the Major Lineages Present in Human Peripheral Blood Mononuclear Cells with Emphasis on the T cell Memory Compartment.
Lily M. Park, Joanne A Lannigan, … Diana Lucia Bonilla·Cytometry Part APeer-reviewed·Oct 28, 2024
- Unveiling the inter individual variability of human fibroblasts innate immune response using robust cell-based protocols
B. David-Watine, A. Chansard, … Milieu interieur Consortium·bioRxiv·Jun 4, 2020
- Multi-parameter spectral flow cytometry panel for immune phenotyping of murine B and T cell responses
Kassandra Hoetzel, Hendrik Feuerstein, … Hedda Wardemann·European Journal of ImmunologyPeer-reviewed·Apr 1, 2026
- 34-parameter full spectrum immunophenotyping panel of human regulatory and effector lymphocytes
Zoya G. Georgieva, Valerie Coppard, … Joanne Jones·bioRxiv·Mar 21, 2024