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Updated: May 24, 2026

Quantification of Monocyte Transmigration and Foam Cell Formation from Individuals with Chronic Inflammatory Conditions
Published on: October 17, 2017
Monocyte subpopulations and cardiovascular risk in chronic kidney disease
Gunnar H Heine1, Alberto Ortiz, Ziad A Massy
1Saarland University Medical Center, Germany. gunnar.heine@uks.eu
Insights
Intermediate monocytes, a specific immune cell type, are linked to cardiovascular disease (CVD) in chronic kidney disease (CKD) patients. Targeting these cells may offer a new therapeutic strategy for reducing CVD risk in this population.
Area of Science:
- Immunology
- Nephrology
- Cardiology
Background:
- Chronic kidney disease (CKD) is associated with a high burden of cardiovascular disease (CVD).
- Monocyte activation and chronic microinflammation are key contributors to CVD in CKD.
- Monocytes are heterogeneous, with three main subsets: classical, intermediate, and nonclassical.
Purpose of the Study:
- To investigate the role of intermediate monocytes in the development of atherosclerosis in CKD patients.
- To explore intermediate monocytes as a potential therapeutic target for CVD in CKD.
Main Methods:
- Analysis of monocyte subset populations (CD14, CD16 expression).
- Review of epidemiological and laboratory data linking monocyte subsets to CKD and CVD outcomes.
- Assessment of chemokine receptor expression and cytokine secretion patterns of intermediate monocytes.
Main Results:
- Intermediate monocytes (CD14(++)CD16(+)) show unique chemokine receptor expression and are prone to secreting proinflammatory cytokines.
- Numbers of intermediate monocytes increase with declining renal function in CKD.
- High counts of intermediate monocytes predict adverse outcomes in both early and advanced CKD stages.
Conclusions:
- Intermediate monocytes play a significant role in atherogenesis and CVD development in CKD patients.
- The abundance of intermediate monocytes correlates with renal function and clinical outcomes.
- Targeting intermediate monocytes presents a promising therapeutic avenue for managing CVD in the CKD population.
Abstract:
Chronic microinflammation and its cellular hallmark, monocyte activation, contribute substantially to the tremendous burden of cardiovascular disease (CVD) in patients with chronic kidney diseases (CKD). Monocyte heterogeneity is widely acknowledged. Cell-surface expression of CD14 and CD16 defines three functionally and phenotypically distinct subsets of monocytes: classical (CD14(++)CD16(-)) monocytes, intermediate (CD14(++)CD16(+)) monocytes, and nonclassical (CD14(+)CD16(++)) monocytes. A growing body of circumstantial evidence suggests that intermediate monocytes, in particular, contribute to the development of atherosclerosis in the general population as well as in patients with CKD. Intermediate monocytes express a unique pattern of chemokine receptors that have been implicated in atherogenesis. Moreover, this subset of monocytes is predisposed to secrete proinflammatory cytokines. Findings from epidemiological studies indicate that numbers of intermediate monocytes increase with worsening renal function, and that high cell counts predict adverse outcomes in patients undergoing dialysis as well as in patients at early stages of CKD. Based on laboratory and clinical data, intermediate monocytes are a promising therapeutic target for CVD in patients with CKD.
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