PMID- 23146450 OWN - NLM STAT- MEDLINE DCOM- 20130613 LR - 20181202 IS - 1873-2623 (Electronic) IS - 0041-1345 (Linking) VI - 44 IP - 9 DP - 2012 Nov TI - Monitoring of circulating antibodies in a renal transplantation population: preliminary results. PG - 2548-50 LID - S0041-1345(12)01054-8 [pii] LID - 10.1016/j.transproceed.2012.09.072 [doi] AB - BACKGROUND: The presence of circulating antibodies (CA) against human leukocyte antigen (HLA) and major-histocompatibility-complex class I-related chain A (MICA) antigens has been associated with worse renal function and reduced kidney allograft survival. We sought to describe the presence of donor-specific anti-HLA antibodies, non-donor specific antibodies, and antibodies against MICA antigens among a cohort of renal transplant recipients with respect to their evolution effects on renal function and occurrence of an acute rejection episode (AR) after transplantation. METHODS: This prospective study of 22 renal transplant recipients of deceased donor kidneys underwent studies of antibodies before and 3 months after grafting using Luminex technology. RESULTS: Ten patients (five men and five women) showed preexistent CA. Comparing patients with versus without preformed CA, we did not observe a significant difference in donor and recipient age or gender. Eight patients (80%) with CA had undergone induction treatment with anti-human-activated T-lymphocyte rabbit immunoglobulin and 2 (20%) with basiliximab. There were no differences between groups regarding the incidence of acute rejection episodes (ARE n = 3 each). There was one case of Banff grade IIB ARE in a patient without preexisting CA; the other episodes were low-grade cellular responses. There were no differences in other variables including cold ischemia time, HLA mismatches, panel-reactive antibody levels, number of transfusions, cytomegalovirus infection or renal function at discharge and 3 months later. Retransplantation was the only factor associated with preformed CA. Retransplantation and preformed CA were associated with CA at 3 months after transplantation. CONCLUSIONS: CA monitoring is important for highly sensitized renal transplants, although our experience failed to show a difference in graft survival or renal function in the first 3 months' follow-up. CI - Copyright (c) 2012 Elsevier Inc. All rights reserved. FAU - Rodriguez Ferrero, M L AU - Rodriguez Ferrero ML AD - Nephrology Department, Hospital General Universitario Gregorio Maranon, Madrid, Spain. mlrodriguezf@senefro.org FAU - Arroyo, D AU - Arroyo D FAU - Panizo, N AU - Panizo N FAU - Vicario, J L AU - Vicario JL FAU - Balas, A AU - Balas A FAU - Anaya, F AU - Anaya F LA - eng PT - Journal Article PL - United States TA - Transplant Proc JT - Transplantation proceedings JID - 0243532 RN - 0 (Antibodies, Monoclonal) RN - 0 (Antilymphocyte Serum) RN - 0 (Biomarkers) RN - 0 (HLA Antigens) RN - 0 (Histocompatibility Antigens Class I) RN - 0 (Immunosuppressive Agents) RN - 0 (Isoantibodies) RN - 0 (MHC class I-related chain A) RN - 0 (Recombinant Fusion Proteins) RN - 9927MT646M (Basiliximab) SB - IM MH - Acute Disease MH - Adult MH - Aged MH - Aged, 80 and over MH - Antibodies, Monoclonal/therapeutic use MH - Antilymphocyte Serum/therapeutic use MH - Basiliximab MH - Biomarkers/blood MH - Female MH - Graft Rejection/epidemiology/immunology/surgery MH - HLA Antigens/*immunology MH - Histocompatibility Antigens Class I/*immunology MH - Humans MH - Immunosuppressive Agents/therapeutic use MH - Incidence MH - Isoantibodies/*blood MH - Kidney Transplantation/adverse effects/*immunology MH - Male MH - Middle Aged MH - Monitoring, Immunologic MH - Prospective Studies MH - Recombinant Fusion Proteins/therapeutic use MH - Reoperation MH - Risk Factors MH - Spain/epidemiology MH - Time Factors MH - Treatment Outcome EDAT- 2012/11/14 06:00 MHDA- 2013/06/14 06:00 CRDT- 2012/11/14 06:00 PHST- 2012/11/14 06:00 [entrez] PHST- 2012/11/14 06:00 [pubmed] PHST- 2013/06/14 06:00 [medline] AID - S0041-1345(12)01054-8 [pii] AID - 10.1016/j.transproceed.2012.09.072 [doi] PST - ppublish SO - Transplant Proc. 2012 Nov;44(9):2548-50. doi: 10.1016/j.transproceed.2012.09.072.