Abstract | OBJECTIVE: METHODS: Peripheral blood mononuclear cells (PBMC) from 26 healthy individuals and 31 patients with inflammatory rheumatic diseases (IRD) were cultured with combinations of CRP, purified or recombinant ss2-GPI, and LPS and monocyte TF procoagulant activity, TF antigen, and TF mRNA were measured. Results were examined against plasma CRP levels. RESULTS: Monocytes from patients with IRD expressed significantly more TF when stimulated with CRP compared to normal monocytes (p = 0.002). An incremental positive correlation was observed between plasma CRP levels and TF induced by CRP or ss2-GPI. Significantly more TF was induced with CRP combined with ss2-GPI, compared to ss2-GPI alone, either with costimulation or CRP priming. Conversely, when combined with LPS, ss2-GPI suppressed TF induction in a dose-dependent manner on normal PBMC but not on PBMC from patients with IRD. The loss of suppression correlated strongly with plasma CRP levels. CONCLUSION: This study shows a remarkably consistent effect of CRP on monocyte TF expression. Systemic inflammation associated with elevated plasma CRP conferred a phenotype on PBMC, whereby incremental priming with respect to TF expression (induced by CRP itself or ss2-GPI) was apparent, and ss2-GPI-mediated inhibition of TF expression induced by LPS was incrementally lost. CRP regulation of monocyte TF could contribute to the higher than expected atherosclerotic vascular disease seen in patients with IRD.
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Authors | Hong Cai, Changjie Song, Irwin Geok San Lim, Steven A Krilis, Carolyn L Geczy, H Patrick McNeil |
Journal | The Journal of rheumatology
(J Rheumatol)
Vol. 32
Issue 7
Pg. 1224-31
(Jul 2005)
ISSN: 0315-162X [Print] Canada |
PMID | 15996056
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Glycoproteins
- Lipopolysaccharides
- beta 2-Glycoprotein I
- C-Reactive Protein
- Thromboplastin
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Topics |
- Adult
- Arteriosclerosis
(immunology, metabolism)
- Arthritis, Rheumatoid
(immunology, metabolism)
- C-Reactive Protein
(immunology, metabolism)
- Cells, Cultured
- Female
- Glycoproteins
(metabolism)
- Humans
- Lipopolysaccharides
(pharmacology)
- Male
- Middle Aged
- Monocytes
(cytology, immunology, metabolism)
- Thromboplastin
(metabolism)
- Up-Regulation
(immunology)
- beta 2-Glycoprotein I
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