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Impact of donor ABH-secretor status in ABO-mismatched living donor kidney transplantation
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3698579
Author(s) Drexler, Beatrice; Holbro, Andreas; Sigle, Joerg; Gassner, Christoph; Frey, Beat M.; Schaub, Stefan; Amico, Patrizia; Plattner, Alexandra; Infanti, Laura; Menter, Thomas; Mihatsch, Michael Jörg; Stern, Martin; Buser, Andreas; Dickenmann, Michael
Author(s) at UniBasel Buser, Andreas
Year 2016
Title Impact of donor ABH-secretor status in ABO-mismatched living donor kidney transplantation
Journal Transfusion
Volume 56
Number 9
Pages / Article-Number 2355-61
Abstract The ABO blood group is a major determinant in living donor kidney transplantation since AB antigens are expressed on renal tissue. Little attention has been directed to the ABH-secretor status of the donor kidney. As renal tissue is capable of secreting soluble ABH antigens in secretors, we examined the influence of the ABH-secretor status of kidney donors on outcome in ABO-mismatched living donor kidney transplantation.; We retrospectively analyzed all patients who underwent ABO-mismatched kidney transplantation at the University Hospital Basel from September 2005 to October 2013. The ABH-secretor status was determined in all donors by molecular genetic analysis.; Of all 55 patients who received transplants, we excluded all patients with donor-specific antibodies (n = 4). Forty-one donors were secretors (78%) and 11 were nonsecretors (22%). Recipients of ABH-secretor donor organs showed a significantly higher glomerular filtration rate throughout the first 6 months posttransplant, whereas no significant influence on posttransplant anti-A/B titers was found. Regression analysis revealed a significant impact on humoral rejection, whereas not on vascular or interstitial rejection in protocol kidney biopsies.; The donor ABH-secretor status may have an influence on early posttransplant renal function in patients undergoing ABO-mismatched living donor kidney transplantation. Further prospective studies with long-term follow-up are needed to elucidate involved pathomechanisms.
Publisher Wiley
ISSN/ISBN 1537-2995
edoc-URL http://edoc.unibas.ch/52184/
Full Text on edoc No
Digital Object Identifier DOI 10.1111/trf.13711
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/27397630
ISI-Number WOS:000385837900029
Document type (ISI) Journal Article
 
   

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