PMID- 21289594 OWN - NLM STAT- MEDLINE DCOM- 20110601 LR - 20110325 IS - 1534-6080 (Electronic) IS - 0041-1337 (Linking) VI - 91 IP - 7 DP - 2011 Apr 15 TI - Effect of immunosuppression for first kidney or kidney/pancreas transplant on sensitization at the time of second transplant. PG - 751-6 LID - 10.1097/TP.0b013e31820cfd5b [doi] AB - BACKGROUND: Previously transplanted patients are more likely to be sensitized, leading to prolonged waitlist times and decreased graft survival. This analysis of the United Network for Organ Sharing kidney/pancreas transplant database investigates factors at the time of first transplant associated with increased sensitization in patients undergoing second transplantation. METHODS: Records of nonsensitized patients (panel reactive antibodies [PRA] <20%) receiving a primary transplant in 1999 or later were analyzed to determine whether immunosuppressive agents at the time of first transplant were associated with a change in PRA from first to second transplant. Variables included gender, race, human leukocyte antigen (HLA) mismatch, rabbit antithymocyte globulin (RATG), interleukin-2 receptor antagonists, tacrolimus (FK), cyclosporine A (CSA), and mycophenolate mofetil/sodium (MMF). RESULTS: For the primary endpoint of increase in PRA greater than or equal to 20%, African Americans (AA) versus non-AA (OR 2.63, P<0.0001) and HLA nonzero mismatch versus zero mismatch (OR 2.90, P<0.0001) were associated with increased sensitization. The effect of immunosuppressive regimen depended on race and HLA status. In non-AAs/HLA mismatch (1-6), interleukin-2 receptor antagonists versus RATG (OR 1.40, P=0.001), CSA versus FK (OR 1.69, P<0.001) and no MMF versus MMF (OR 1.39, P<0.001) were also associated with increased sensitization. In AAs/HLA mismatch (1-6), no induction versus RATG (OR 1.59, P=0.031) and CSA versus FK (OR 1.68, P=0.006) were associated with increased sensitization. CONCLUSIONS: These data suggest a reduced risk of sensitization at the time of second transplant when using more potent immunosuppression with RATG, FK, and MMF for nonsensitized primary kidney or kidney/pancreas transplant patients. These effects seem to be related to race and HLA mismatch. FAU - Dawson, Kyle L AU - Dawson KL AD - Department of Pharmacy, The Methodist Hospital, Houston, TX. 2Center for Biostatistics, The Methodist Hospital Research Institute, Houston, TX 77030, USA. KLDawson@tmhs.org FAU - Patel, Samir J AU - Patel SJ FAU - Xu, Jiaqiong AU - Xu J FAU - Knight, Richard J AU - Knight RJ FAU - Gaber, A Osama AU - Gaber AO LA - eng PT - Journal Article PL - United States TA - Transplantation JT - Transplantation JID - 0132144 RN - 0 (Antilymphocyte Serum) RN - 0 (Immunosuppressive Agents) RN - 0 (Receptors, Interleukin-2) SB - IM MH - Adult MH - Antilymphocyte Serum/pharmacology MH - Female MH - Graft Survival MH - Histocompatibility Testing MH - Humans MH - Immunosuppressive Agents/*pharmacology MH - Kidney Transplantation/*immunology MH - Male MH - Middle Aged MH - Pancreas Transplantation/*immunology MH - Receptors, Interleukin-2/antagonists & inhibitors MH - Transplantation, Homologous EDAT- 2011/02/04 06:00 MHDA- 2011/06/02 06:00 CRDT- 2011/02/04 06:00 PHST- 2011/02/04 06:00 [entrez] PHST- 2011/02/04 06:00 [pubmed] PHST- 2011/06/02 06:00 [medline] AID - 10.1097/TP.0b013e31820cfd5b [doi] PST - ppublish SO - Transplantation. 2011 Apr 15;91(7):751-6. doi: 10.1097/TP.0b013e31820cfd5b.