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Phagocytic cell function as an index of biocompatibility
1Division of Nephrology, School of Medicine, University of Louisville, Kentucky 40292.
Summary
Phagocyte function changes during hemodialysis, but linking these to specific dialysis membranes is difficult. More research is needed to understand the impact of membrane properties on biocompatibility and immune cell responses.
Area of Science:
- Immunology
- Biomaterials Science
- Nephrology
Background:
- Phagocytic cells play a crucial role in the immune response.
- Biocompatibility assessment of medical devices often involves evaluating cellular functions.
- Hemodialysis involves interactions between blood and artificial membranes, potentially affecting immune cells.
Purpose of the Study:
- To review the physiology and biochemistry of phagocytic cells.
- To examine the rationale for using phagocyte function to assess biocompatibility.
- To analyze the impact of hemodialysis membranes on phagocyte function and biocompatibility.
Main Methods:
- Review of existing literature on phagocyte physiology and biochemistry.
- Analysis of studies investigating phagocyte responses during hemodialysis.
- Examination of the relationship between dialysis membrane properties and phagocyte function.
Main Results:
- Hemodialysis modulates phagocyte adhesion receptors, influenced by complement activation.
- Changes in circulating phagocyte numbers are linked to pulmonary sequestration.
- The role of membrane material, mass transfer, and dialysate quality in monocyte cytokine production is unclear.
- Distinguishing dialysis effects from uremia effects on chronic phagocyte function is challenging.
Conclusions:
- Changes in circulating phagocyte numbers and adhesion receptor expression are useful biocompatibility indicators.
- A definitive link between specific membrane properties and other phagocyte function changes remains to be established.
- Further well-designed studies are required to clarify the impact of dialysis membranes on phagocyte function and biocompatibility.