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Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis
Published on: October 17, 2018
Monocyte subsets predict mortality after cardiac arrest
Konstantin A Krychtiuk1, Max Lenz1, Bernhard Richter1
1Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Insights
Immune cell changes after cardiac arrest impact survival. Intermediate monocytes (IM) increase in non-survivors 72 hours post-cardiac arrest, suggesting a role for innate immunity in post-cardiac arrest syndrome.
Area of Science:
- Immunology
- Critical Care Medicine
- Cardiology
Background:
- Post-successful cardiopulmonary resuscitation (CPR), patients often exhibit heightened immune activation.
- Monocytes, key immune cells, comprise distinct subsets: classical (CM), intermediate (IM), and non-classical (NCM), identifiable by flow cytometry.
- Understanding these monocyte subsets may offer insights into post-cardiac arrest outcomes.
Purpose of the Study:
- To investigate the association between monocyte subset distribution and clinical outcomes in patients following cardiac arrest.
- To determine if specific monocyte subsets can predict survival and neurological function at 6 months post-cardiac arrest.
Main Methods:
- A cohort of 53 medical intensive care unit (ICU) patients admitted after cardiac arrest was studied.
- Blood samples were collected on ICU admission and at 72 hours.
- Monocyte subsets (CM, IM, NCM) were analyzed using flow cytometry, with primary endpoints of 6-month survival and neurological outcome (CPC score).
Main Results:
- Six-month mortality was 50.9%, with 37.7% achieving good neurological outcome.
- Monocyte subset distribution on admission did not correlate with survival.
- At 72 hours, non-survivors showed a higher percentage of pro-inflammatory IM and a lower percentage of CM compared to survivors.
- IM subset levels independently predicted outcome and correlated with the cerebral performance category (CPC) score.
Conclusions:
- The distribution of monocyte subsets, particularly the pro-inflammatory IM, changes significantly by 72 hours post-cardiac arrest in non-survivors.
- Intermediate monocytes may serve as a predictive biomarker for outcomes in post-cardiac arrest patients.
- These findings highlight a potential role for the innate immune system in the pathophysiology of post-cardiac arrest syndrome.
Abstract:
After successful cardiopulmonary resuscitation (CPR), many patients show signs of an overactive immune activation. Monocytes are a heterogeneous cell population that can be distinguished into 3 subsets by flow cytometry (classical monocytes [CM: CD14++ CD16- ], intermediate monocytes [IM: CD14++ CD16+ CCR2+ ] and non-classical monocytes [NCM: CD14+ CD16++ CCR2- ]). Fifty-three patients admitted to the medical intensive care unit (ICU) after cardiac arrest were included. Blood was taken on admission and after 72 h. The primary endpoint of this study was survival at 6 months and the secondary endpoint was neurological outcome as determined by cerebral performance category (CPC)-score at 6 months. Median age was 64.5 (49.8-74.3) years and 75.5% were male. Six-month mortality was 50.9% and survival with good neurological outcome was 37.7%. Monocyte subset distribution upon admission to the ICU did not differ according to survival. Seventy-two hours after admission, patients who died within 6 months showed a higher percentage of the pro-inflammatory subset of IM (8.3% [3.8-14.6]% vs. 4.1% [1.5-8.2]%; P = 0.025), and a lower percentage of CM (87.5% [79.9-89.0]% vs. 90.8% [85.9-92.7]%; P = 0.036) as compared to survivors. In addition, IM were predictive of outcome independent of time to ROSC and witnessed cardiac arrest, and correlated with CPC-score at 6 months (R = 0.32; P = 0.043). These findings suggest a possible role of the innate immune system in the pathophysiology of post cardiac arrest syndrome.
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