Premium
Comparison of two different strategies for human monocyte subsets gating within the large‐scale prospective CARE FOR HOM e Study
Author(s) -
Zawada Adam M.,
Fell Lisa H.,
Untersteller Kathrin,
Seiler Sarah,
Rogacev Kyrill S.,
Fliser Danilo,
ZieglerHeitbrock Loems,
Heine Gunnar H.
Publication year - 2015
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.22703
Subject(s) - gating , monocyte , cd14 , quartile , cd16 , confounding , medicine , prospective cohort study , oncology , immunology , receptor , confidence interval , immune system , cd8 , physiology , cd3
Monocytes are heterogeneous cells consisting of (at least) three subsets: classical, intermediate, and nonclassical monocytes. Correct enumeration of cell counts necessitates well‐defined gating strategies, which are essentially based upon CD14 and CD16 expression. For the delineation of intermediate from nonclassical monocytes, a “rectangular gating (RG) strategy” and a “trapezoid gating (TG) strategy” have been proposed. We compared the two gating strategies in a well‐defined clinical cohort of patients with chronic kidney disease (CKD). Within the ongoing CARE FOR HOMe study, monocyte subsets were reanalyzed in 416 CKD patients, who were followed 3.6 ± 1.6 years for the occurrence of a cardiovascular event. Gating was performed by either RG or TG. We analyzed the expression of surface markers, and compared the predictive role of cell counts of monocyte subsets, as defined by RG and TG, respectively. With both gating strategies, higher intermediate monocyte counts predicted the cardiovascular endpoint in Kaplan‐Meier analyses ( P < 0.001 with RG; P < 0.001 with TG). After correction for confounders, intermediate monocyte counts remained independent predictors in Cox‐Regression analyses (HR = 1.013 [95% CI: 1.006–1.020; P < 0.001] with RG; HR = 1.015 [95% CI: 1.006–1.024; P = 0.001] with TG). NRI was 3.9% when reclassifying patients from quartiles of intermediate monocyte counts with RG strategy toward quartiles of intermediate monocytes counts with TG strategy. In expression analysis, those monocytes which are defined as intermediate monocytes by the RG strategy and as nonclassical monocytes by the TG strategy share characteristics of both subsets. In conclusion, intermediate monocytes were independent predictors of cardiovascular outcome irrespective of the applied gating strategy. Future studies should aim to identify markers that allow for an unequivocal definition of intermediate monocytes, which may further improve their power to predict cardiovascular events. © 2015 International Society for Advancement of Cytometry