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Living donor kidney transplantation in patients with donor-specific HLA antibodies enabled by anti-CD20 therapy and peritransplant apheresis
Authors:Katrin Klein  Caner Süsal  Sebastian M. Schäfer  Luis Eduardo Becker  Jörg Beimler  Vedat Schwenger  Martin Zeier  Peter Schemmer  Stephan Macher-Goeppinger  Sabine Scherer  Gerhard Opelz  Christian Morath
Affiliation:1. Department of Nephrology, University of Heidelberg, INF 162, 69120 Heidelberg, Germany;2. Transplantation Immunology, University of Heidelberg, INF 305, 69120 Heidelberg, Germany;3. Transplantation Surgery, University of Heidelberg, INF 110, 69120 Heidelberg, Germany;4. Department of Pathology, University of Heidelberg, INF 224, 69120 Heidelberg, Germany
Abstract:ObjectiveDue to increasing waiting times for deceased donor kidneys, living donor kidney transplantation is increasingly performed in the presence of donor-specific antibodies (DSA).MethodsTwenty-three patients with Luminex-detected DSA were successfully desensitized by anti-CD20 therapy and immunoadsorption (N = 19) or plasmapheresis (N = 4) and received a kidney transplant from a living donor. Twelve of the 23 patients (52%) had a positive CDC and/or ELISA crossmatch result before desensitization. Six patients were negative in CDC as well as ELISA screening but positive in Luminex for DSA.ResultsThe 23 patients received a median of 8 apheresis treatments before and 5 treatments after transplantation. Induction therapy was performed with either thymoglobulin (N = 11) or basiliximab (N = 12). The 2-year graft survival rate was 100%. At last follow up, a median of 12 months after transplantation, median serum creatinine was 1.42 mg/dL, median MDRD-GFR 59.5 mL/min/1.73 m2, and median urinary protein-to-creatinine ratio 0.12. Ten out of fourteen patients (71%) who had completed the first year after transplantation by the time of analysis had no DSA by day 360. Acute T-cell mediated rejection was diagnosed in one patient (4%), and antibody-mediated changes were found in 5 patients (22%). Four out of these 5 patients showed evidence of persistent (N = 2) or reemerging plus/minus de novo DSA (N = 2) on day 360, and the 2 patients with persistent DSA lost their allograft subsequently on days 750 and 810, respectively. Infectious complications were infrequent.ConclusionsOur previously described treatment algorithm for desensitization of living donor kidney transplant recipients with DSA results in good graft outcomes with a low rate of side effects.
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