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Phenotypic Landscape of Immune Cells in Sepsis: Insights from High-Dimensional Mass Cytometry.

Authors :
Park S
Perumalsamy H
Gerelkhuu Z
Sunderraj S
Lee Y
Yoon TH
Source :
ACS infectious diseases [ACS Infect Dis] 2024 Jul 12; Vol. 10 (7), pp. 2390-2402. Date of Electronic Publication: 2024 Jun 08.
Publication Year :
2024

Abstract

Understanding the sepsis-induced immunological response can be facilitated by identifying phenotypic changes in immune cells at the single-cell level. Mass cytometry, a novel multiparametric single-cell analysis technique, offers considerable benefits in characterizing sepsis-induced phenotypic changes in peripheral blood mononuclear cells. Here, we analyzed peripheral blood mononuclear cells from 20 sepsis patients and 10 healthy donors using mass cytometry and employing 23 markers. Both manual gating and automated clustering approaches (PhenoGraph) were used for cell identification, complemented by uniform manifold approximation and projection (UMAP) for dimensionality reduction and visualization. Our study revealed that patients with sepsis exhibited a unique immune cell profile, marked by an increased presence of monocytes, B cells, and dendritic cells, alongside a reduction in natural killer (NK) cells and CD4/CD8 T cells. Notably, significant changes in the distributions of monocytes and B and CD4 T cells were observed. Clustering with PhenoGraph unveiled the subsets of each cell type and identified elevated CCR6 expression in sepsis patients' monocyte subset (PG#5), while further PhenoGraph clustering on manually gated T and B cells discovered sepsis-specific CD4 T cell subsets (CCR4 <superscript>low</superscript> CD20 <superscript>low</superscript> CD38 <superscript>low</superscript> ) and B cell subsets (HLA-DR <superscript>low</superscript> CCR7 <superscript>low</superscript> CCR6 <superscript>high</superscript> ), which could potentially serve as novel diagnostic markers for sepsis.

Details

Language :
English
ISSN :
2373-8227
Volume :
10
Issue :
7
Database :
MEDLINE
Journal :
ACS infectious diseases
Publication Type :
Academic Journal
Accession number :
38850242
Full Text :
https://doi.org/10.1021/acsinfecdis.4c00066