TY - JOUR
TI - Single-Cell Analysis of Human Mononuclear Phagocytes Reveals Subset-Defining Markers and Identifies Circulating Inflammatory Dendritic Cells
AU - Dutertre, C.-A.
AU - Becht, E.
AU - Irac, S.E.
AU - Khalilnezhad, A.
AU - Narang, V.
AU - Khalilnezhad, S.
AU - Ng, P.Y.
AU - van den Hoogen, L.L.
AU - Leong, J.Y.
AU - Lee, B.
AU - Chevrier, M.
AU - Zhang, X.M.
AU - Yong, P.J.A.
AU - Koh, G.
AU - Lum, J.
AU - Howland, S.W.
AU - Mok, E.
AU - Chen, J.
AU - Larbi, A.
AU - Tan, H.K.K.
AU - Lim, T.K.H.
AU - Karagianni, P.
AU - Tzioufas, A.G.
AU - Malleret, B.
AU - Brody, J.
AU - Albani, S.
AU - van Roon, J.
AU - Radstake, T.
AU - Newell, E.W.
AU - Ginhoux, F.
JO - Pathogens and Immunity
PY - 2019
VL - 51
TODO - 3
SP - 573-589.e8
PB - Cell Press
SN - null
TODO - 10.1016/j.immuni.2019.08.008
TODO - biological marker;  CD14 antigen;  CD163 antigen;  CD5 antigen;  cell protein;  Fc receptor;  HLA DQ antigen;  RNA;  biological marker;  leukocyte antigen, Article;  cell heterogeneity;  controlled study;  dendritic cell;  disease activity;  disease exacerbation;  human;  human cell;  immunopathology;  inflammatory cell;  monocyte;  mononuclear phagocyte;  phenotype;  priority journal;  single cell analysis;  systemic lupus erythematosus;  blood;  cell culture;  dendritic cell;  flow cytometry;  immunology;  inflammation;  mononuclear cell;  phagocyte;  procedures;  single cell analysis, Antigens, CD;  Biomarkers;  Cells, Cultured;  Dendritic Cells;  Flow Cytometry;  Humans;  Inflammation;  Leukocytes, Mononuclear;  Lupus Erythematosus, Systemic;  Monocytes;  Phagocytes;  Phenotype;  Single-Cell Analysis
TODO - Human mononuclear phagocytes comprise phenotypically and functionally overlapping subsets of dendritic cells (DCs) and monocytes, but the extent of their heterogeneity and distinct markers for subset identification remains elusive. By integrating high-dimensional single-cell protein and RNA expression data, we identified distinct markers to delineate monocytes from conventional DC2 (cDC2s). Using CD88 and CD89 for monocytes and HLA-DQ and FcεRIα for cDC2s allowed for their specific identification in blood and tissues. We also showed that cDC2s could be subdivided into phenotypically and functionally distinct subsets based on CD5, CD163, and CD14 expression, including a distinct subset of circulating inflammatory CD5−CD163+CD14+ cells related to previously defined DC3s. These inflammatory DC3s were expanded in systemic lupus erythematosus patients and correlated with disease activity. These findings further unravel the heterogeneity of DC subpopulations in health and disease and may pave the way for the identification of specific DC subset-targeting therapies. Using high-dimensional protein and RNA single-cell analyses, Dutertre et al. analyze human dendritic cell and monocyte subsets and identify markers that delineate them and unravel their heterogeneity. They also reveal the presence of inflammatory CD14+ DC3s, a subset of cDC2s, that correlate with disease progression and may be functionally involved in systemic lupus erythematosus immunopathology. © 2019 Elsevier Inc.
ER -