Abstract

Background: Antibodies directed against donor mismatched Human Leucocyte Antigens (HLA) are known to cause antibody-mediated rejection and affect the graft survival of transplanted organs. The influence of donor-directed antibodies against the products of HLA class I and II genes in renal transplantation are well described for class I (HLA-A, B and C), but still not clear for class II notably HLA DP. The clinical effects of donor-specific antibodies (DSA) directed against HLA-DP are still controversial.Methods: We report the outcome of kidney transplants in three highly sensitised individuals with significant sensitisation with donor-directed HLA-DP antibody. These recipients were on the waiting list for 6, 14 and 4 years, respectively and had kidney transplants from donors after brain death (DBD) with positive B cell flow cytometry crossmatch (FCXM). Two cases received induction therapy with a depleting antibody (Thymoglobulin®) while the third received Alemtuzumab followed by standard immunosuppression.Results: The clinical course of these three patients were different. The first patient developed transplant glomerulopathy, but the graft is still functioning with eGFR 29 mL/min/1.73 m2. The second patient did not have any adverse event with eGFR 26 mL/min/1.73 m2, while the third patient had severe antibody-mediated rejection (AMR), which was treated successfully with eGFR 32 mL/min/1.73 m2.Conclusion: Patients waiting for a deceased allograft with HLA-DP DSA and a positive FCXM can be transplanted successfully with depleting antibody or Alemtuzumab induction without prior antibody removal followed by standard immunosuppression.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.