Abstract

Monocytes play an important role in both innate immunity and antigen presentation for specific cellular immune defense. In patients with chronic renal failure, as well as those treated with maintenance hemodialysis, these cells are largely dysregulated. There is a large body of literature on monocyte alterations in such patients. However, most of the publications report on small series, there is a vast spectrum of different methods and the heterogeneity of the data prevents any meta-analytic approach. Thus, a narrative review was performed to describe the current knowledge. Monocytes from patients with chronic renal failure differ from those of healthy individuals in the pattern of surface molecule expression, cytokine and mediator production, and function. If these findings can be summarized at all, they might be subsumed as showing chronic inflammation in resting cells together with limited activation upon immunologic challenge. The picture is complicated by the fact that monocytes fall into morphologically and functionally different populations and population shifts interact heavily with dysregulation of the individual cells. Severe complications of chronic renal failure such as impaired immune defense, inflammation, and atherosclerosis can be related to several aspects of monocyte dysfunction. Therefore, this review aims to provide an overview about the impairment and activation of monocytes by uremia and the resulting clinical consequences for renal failure patients.

Highlights

  • Monocytes are bone marrow derived cells that circulate in the blood for 1–3 days before differentiating into tissue macrophages or dendritic cells

  • This review aims firstly to describe the structural and functional abnormalities observed in monocytes from chronic kidney disease (CKD) patients, secondly to review the mechanism by which CKD affects monocytes populations and fundamental monocytic functions and thirdly to explain how these alterations may impact both antimicrobial defense and atherosclerosis development in this population

  • A decrease of phagocytic capabilities, impairment of antigen presentation function on the one side and elevation of inflammatory markers and specialized monocyte subsets on the other side characterize the monocyte momentum in CKD

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Summary

Introduction

Monocytes are bone marrow derived cells that circulate in the blood for 1–3 days before differentiating into tissue macrophages or dendritic cells. They are part of the innate immune system and react quickly but unspecifically to any tissue damage or pathogen intrusion. They produce cytokines that regulate inflammatory responses Among their most important functions are chemotaxis, which describes the approach to sites of tissue damage in response to soluble mediators and cytokines, as well as adhesion and transmigration through the endothelium. The latter is promoted by specific adhesion molecules that bind to endothelial ligands

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