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Autor(en) / Beteiligte
Titel
Interleukin-12 and -18 Levels in Peritoneal Dialysate Effluent Correlate With the Outcome of Peritonitis in Patients Undergoing Peritoneal Dialysis: Implications for the Type I/Type II T-Cell Immune Response
Ist Teil von
  • American journal of kidney diseases, 2005-08, Vol.46 (2), p.328-338
Ort / Verlag
Orlando, FL: Elsevier Inc
Erscheinungsjahr
2005
Quelle
MEDLINE
Beschreibungen/Notizen
  • Background: We previously showed that a positive impact of peritoneal defense response on the outcome of peritoneal dialysis (PD)-related peritonitis is characterized by an increased pattern of peritoneal CD4/CD8 T-cell ratio with a predominant CD4 +-T helper subtype 1 phenotype. To further explore longitudinal changes in peritoneal immunity during PD-related peritonitis, we examined the production of interleukin 12 (IL-12), IL-18, and interferon γ (IFN-γ) in peritoneal dialysate effluent (PDE) and kinetic expression of the transcription factors T box expressed in T cells (T-bet) and guanine adenine thymine adenine (GATA) binding protein 3 (GATA-3) in peritoneal T cells during peritonitis. Correlations between these observations and responses to antibiotics were analyzed. Methods: IL-12, IL-18, and IFN-γ protein and IFN-γ, T-bet, and GATA-3 messenger RNA (mRNA) were measured in PDE during various phases of peritonitis in 40 patients undergoing PD. Patients were divided into 2 groups according to whether they had a rapid versus delayed response to antibiotic treatment. Results: In the early phase of peritonitis, IL-12, IL-18, and IFN-γ levels in PDE were significantly greater in the rapid-response group ( P < 0.05). Changes in peritoneal IL-12 and IL-18 levels preceded changes in IFN-γ levels. The kinetics of IFN-γ, T-bet, and GATA-3 mRNA expression in peritoneal T cells, measured by means of real-time polymerase chain reaction, differed between the 2 groups. In the rapid-response group, IFN-γ and T-bet mRNA expression increased, whereas that of GATA-3 decreased over time. Results were opposite in the delayed-response group, with IFN-γ and T-bet levels decreasing and GATA-3 levels increasing over time. Conclusion: These data suggest that local IL-12 and IL-18 production is part of a protective early immune response to PD-related peritonitis. High IL-12 and IL-18 levels in PDE during the early phase of peritonitis correlated with a predominant type 1 immune response and favorable outcome.
Sprache
Englisch
Identifikatoren
ISSN: 0272-6386
eISSN: 1523-6838
DOI: 10.1053/j.ajkd.2005.05.008
Titel-ID: cdi_proquest_miscellaneous_68497694
Format
Schlagworte
Abdomen, Adult, Ascitic Fluid - chemistry, Ascitic Fluid - cytology, Biological and medical sciences, Cephalosporins - therapeutic use, DNA-Binding Proteins - analysis, DNA-Binding Proteins - genetics, DNA-Binding Proteins - metabolism, Drug Therapy, Combination - therapeutic use, Female, Gastroenterology. Liver. Pancreas. Abdomen, GATA3 Transcription Factor, Gram-Negative Bacterial Infections - drug therapy, Gram-Negative Bacterial Infections - etiology, Gram-Negative Bacterial Infections - immunology, Gram-Negative Bacterial Infections - metabolism, Gram-Positive Bacterial Infections - drug therapy, Gram-Positive Bacterial Infections - etiology, Gram-Positive Bacterial Infections - immunology, Gram-Positive Bacterial Infections - metabolism, Humans, interferon γ (INF-γ), Interferon-gamma - analysis, Interferon-gamma - genetics, Interleukin 12 (IL-12), interleukin 18 (IL-18), Interleukin-12 - analysis, Interleukin-18 - analysis, Kidney Failure, Chronic - complications, Kidney Failure, Chronic - therapy, Leukocyte Count, Male, Medical sciences, Middle Aged, Nephrology. Urinary tract diseases, Other diseases. Semiology, peritoneal dialysis (PD), Peritoneal Dialysis, Continuous Ambulatory - adverse effects, peritonitis, Peritonitis - drug therapy, Peritonitis - etiology, Peritonitis - immunology, Peritonitis - metabolism, RNA, Messenger - analysis, T box expressed in T cells (T-bet), T-Box Domain Proteins, T-Lymphocyte Subsets - metabolism, Teicoplanin - therapeutic use, Th1 Cells - immunology, Th1 Cells - metabolism, Th2 Cells - immunology, Th2 Cells - metabolism, Trans-Activators - analysis, Trans-Activators - genetics, Trans-Activators - metabolism, Transcription Factors - analysis, Transcription Factors - genetics, Transcription Factors - metabolism, Treatment Outcome

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