| Literature DB >> 29981209 |
David F Pinelli1, Andrea A Zachary2, John J Friedewald3, David W Gjertson4, Michelle A Evans1, Erik N Chatroop1, Mary S Leffell2, Ashley A Vo5, Stanley C Jordan5, Robert A Montgomery2, Anat R Tambur1.
Abstract
Currently, the ability to predict or monitor the efficacy of HLA antibody-removal therapies is deficient. We previously reported that titration studies are a consistent and accurate means of assessing antibody strength. To test whether titration studies can also predict which patients are better candidates for desensitization, we studied 38 patients from 3 centers (29 receiving plasmapheresis/low-dose intravenous immunoglobulin [IVIg]; 9 patients receiving high-dose IVIg). For patients undergoing plasmapheresis/low-dose IVIg, antibody titer reduction correlated with number of treatment cycles for both class I and II antibodies but only up to approximately 4 cycles. Reduction in titer slowed with additional cycles, suggesting a limit to the efficacy of this approach. Furthermore, initial titer (predesensitization) can guide the selection of candidates for successful antibody-removal treatment. In our experience, patients with antibodies at an initial titer >1:512 could not be reduced to the goal of a negative lymphocyte crossmatch, corresponding to a 1:16 titer, despite a significant increase in the number of treatment cycles. Change in mean fluorescence intensity (MFI) value did not correlate with success of treatment if initial MFI values were >10 000, likely due to single antigen bead saturation. Overall, we present a potential prognostic tool to predict candidacy and a monitoring tool to assess efficacy of desensitization treatment.Entities:
Keywords: alloantibody; clinical research/practice; desensitization; histocompatibility; immunosuppression/immune modulation; intravenous immunoglobulin/IVIg; kidney transplantation/nephrology; plasmapheresis/plasma exchange; rejection: antibody-mediated (ABMR); translational research/science
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Year: 2018 PMID: 29981209 DOI: 10.1111/ajt.15007
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086