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Träfflista för sökning "WFRF:(Adrian Katrin 1966) srt2:(2005-2009)"

Sökning: WFRF:(Adrian Katrin 1966) > (2005-2009)

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1.
  • Adrian, Katrin, 1966, et al. (författare)
  • Procedure-induced inflammation and endothelial cell activation in an artificially ventilated and circulated porcine double-lung model
  • 2006
  • Ingår i: Artif Organs. - 0160-564X. ; 30:12, s. 922-8
  • Tidskriftsartikel (refereegranskat)abstract
    • Systemic inflammation is induced during extracorporeal circulation, resulting in an increased bleeding tendency and endothelial cell activation. Lungs from seven piglets were perfused by autologous blood in an extracorporeal circuit, where the lungs and the left atrium were attached to polyvinyl chloride (PVC) tubings and the blood circulated by a roller pump. The trachea was intubated and attached to a ventilator. The lungs maintained good gas exchange, despite a slight increase in lactate levels. Plasma tPA increased slightly over time, suggesting endothelial cell activation. Activation of inflammatory systems was reflected in increased levels of plasma interleukin (IL)-6 and IL-10. A model for the study of lung endothelial activation during extracorporeal circulation has been shown to be reproducible. The lung tissue was shown to be capable of gas exchange and activation of endothelial cells and procedure-induced inflammation were noted.
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3.
  • Galeotti, L, et al. (författare)
  • Circulating survivin indicates severe course of juvenile idiopathic arthritis.
  • 2008
  • Ingår i: Clinical and experimental rheumatology. - 0392-856X. ; 26:2, s. 373-8
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Survivin is an anti-apoptotic protein that has been recently suggested as a predictive marker of joint destruction in adult rheumatoid arthritis. We assessed the presence of extracellular survivin in patients with juvenile idiopathic arthritis (JIA). METHODS: Survivin levels were assessed in the circulation of 46 patients with JIA and in the age- and gender-matched controls (n=46) having no inflammatory disease, by ELISA. Survivin levels were analyzed with respect to the onset type and the activity of the joint disease. The intensity of inflammation and cartilage turnover was measured as levels of IL-6, serum amyloid A protein (SAA), and cartilage oligomeric matrix protein (COMP), respectively. RESULTS: The levels of extracellular survivin were significantly higher in JIA compared to the controls (p=0.0002). High levels of survivin (above mean + 2SD of the controls) were detected in 8/46 (17% JIA patients. High survivin expression was associated with polyarticular onset, active phase of arthritis. In contrast, survivin was neither related to the levels of IL-6, SAA, nor to COMP. CONCLUSION: Circulating survivin is expressed in a significant group of patients with JIA being associated to a severe course of the disease. It may be potentially used to select children with unfavorable prognosis of JIA who are in need of active pharmacologic treatment.
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