Journalartikel
Autorenliste: Pfleger, Christian; Schloot, Nanette C.; Brendel, Mathias D.; Burkart, Volker; Hogenkamp, Viktor; Bretzel, Reinhard G.; Jaeger, Clemens; Eckhard, Michael
Jahr der Veröffentlichung: 2011
Seiten: 154-161
Zeitschrift: Clinical Immunology
Bandnummer: 138
Heftnummer: 2
ISSN: 1521-6616
eISSN: 1521-7035
DOI Link: https://doi.org/10.1016/j.clim.2010.10.008
Verlag: Elsevier
Islet cell transplantation has considerable potential as a cure for type 1 diabetes, but recurrent autoimmunity and allograft rejection in which both cytokines play an important role are major obstacles. Using a new approach considering confounders by regression analysis, we investigated circulating cytokines and their association with graft function in type 1 diabetes patients who underwent either simultaneous islet kidney (SIK) or islet after kidney (IAK) transplantation. After transplantation, interleukin (IL)-10 was lower in SIK recipients with subsequent loss of graft function in comparison to recipients maintaining graft function. Before transplantation, high IL-13 and IL-18 concentrations were prospectively associated for subsequent loss of graft function in IAK recipients, whereas in SIK recipients, high macrophage migration inhibitory factor (MIF) concentrations were associated with subsequent loss of graft function. Circulating cytokines are associated with islet graft function in patients with long-standing type 1 diabetes when considering confounders. (C) 2010 Elsevier Inc. All rights reserved.
Abstract:
Zitierstile
Harvard-Zitierstil: Pfleger, C., Schloot, N., Brendel, M., Burkart, V., Hogenkamp, V., Bretzel, R., et al. (2011) Circulating cytokines are associated with human islet graft function in type 1 diabetes, Clinical Immunology, 138(2), pp. 154-161. https://doi.org/10.1016/j.clim.2010.10.008
APA-Zitierstil: Pfleger, C., Schloot, N., Brendel, M., Burkart, V., Hogenkamp, V., Bretzel, R., Jaeger, C., & Eckhard, M. (2011). Circulating cytokines are associated with human islet graft function in type 1 diabetes. Clinical Immunology. 138(2), 154-161. https://doi.org/10.1016/j.clim.2010.10.008
Schlagwörter
ALLOGRAFT-REJECTION; C-PEPTIDE; ISLET TRANSPLANTATION; MIGRATION INHIBITORY FACTOR; Regenerative therapy; TRANSPLANTATION