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Peritoneal macrophages during peritonitis. Phenotypic studies
- Source :
- Clinical and Experimental Immunology. 88:484-491
- Publication Year :
- 1992
- Publisher :
- Oxford University Press (OUP), 1992.
-
Abstract
- SUMMARY The expression of a range of surface molecules/receptors that are important in the host response to infection and foreign antigens was examined using peritoneal macrophages isolated from patients on continuous ambulatory peritoneal dialysis (CAPD) with peritonitis. The macrophage phenolypic profile was compared with that of normal peripheral blood monocytes. Consistently there was increased expression by macrophages of CD14, ICAM-1 (CD54). FcγRI (CD64). FcγRII (CDw32), FcγRIII (CD 16), transferrin receptors (CD71)and tissue factor. Increased expression of MHC class II was marginally significant. There was no detectable expression of either the p55 (CD25) or p70 chains of the IL-2 receptor. The expression of the complement receptors. CRI (CD35) and CR3 (CD11b. CDI8), was reduced. The activity of well-known inflammatory cytokines, rather than uraemic molecules, can account for the phenotypic profile of these extravasated peritoneal macrophages. The results of this study indicate that peritoneal macrophages from CAPD patients with peritonitis display a phenotype consistent with them being in vivo-derived inflammatory macrophages, and that they arc appropriate for use in studies of anti-inflammatory agents.
- Subjects :
- CD14
Immunology
Peritonitis
Inflammation
Receptors, Fc
CD16
Monocytes
Immunophenotyping
Thromboplastin
Proinflammatory cytokine
Antigens, CD
medicine
Humans
Immunology and Allergy
Macrophage
Receptor
Peritoneal Cavity
business.industry
Macrophages
Histocompatibility Antigens Class I
Continuous ambulatory peritoneal dialysis
Histocompatibility Antigens Class II
hemic and immune systems
Receptors, Interleukin-2
Flow Cytometry
medicine.disease
Receptors, Complement
Immunoglobulin G
medicine.symptom
business
Biomarkers
Research Article
Subjects
Details
- ISSN :
- 13652249 and 00099104
- Volume :
- 88
- Database :
- OpenAIRE
- Journal :
- Clinical and Experimental Immunology
- Accession number :
- edsair.doi.dedup.....7cb4774297f2b4caa658598bc018c03a