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Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study

2018; Elsevier BV; Volume: 18; Issue: 6 Linguagem: Inglês

10.1111/ajt.14594

1600-6143

María P. Hernández-Fuentes, Christopher Franklin, Irene Rebollo‐Mesa, J Mollon, Florence Delaney, Esperanza Perucha, Caragh P. Stapleton, Richard Borrows, Catherine Byrne, Gianpiero L. Cavalleri, Brendan Clarke, Menna R. Clatworthy, John Feehally, Susan V. Fuggle, Sarah A. Gagliano Taliun, Siân Griffin, Abdul Hammad, Robert Higgins, Alan G. Jardine, Mary T. Keogan, Timothy Leach, Iain MacPhee, Patrick B. Mark, James E. Marsh, Alexander P. Maxwell, William McKane, Adam McLean, Charles G. Newstead, Titus Augustine, Paul J. Phelan, S Powis, Peter A. Rowe, Neil Sheerin, Ellen Solomon, Henry Stephens, Raj Thuraisingham, Richard C. Trembath, Peter Topham, R. S. Vaughan, Steven H. Sacks, Peter J. Conlon, Gerhard Opelz, Nicole Soranzo, Michael E. Weale, Graham M. Lord,

Viral-associated cancers and disorders

Improvements in immunosuppression have modified short-term survival of deceased-donor allografts, but not their rate of long-term failure. Mismatches between donor and recipient HLA play an important role in the acute and chronic allogeneic immune response against the graft. Perfect matching at clinically relevant HLA loci does not obviate the need for immunosuppression, suggesting that additional genetic variation plays a critical role in both short- and long-term graft outcomes. By combining patient data and samples from supranational cohorts across the United Kingdom and European Union, we performed the first large-scale genome-wide association study analyzing both donor and recipient DNA in 2094 complete renal transplant-pairs with replication in 5866 complete pairs. We studied deceased-donor grafts allocated on the basis of preferential HLA matching, which provided some control for HLA genetic effects. No strong donor or recipient genetic effects contributing to long- or short-term allograft survival were found outside the HLA region. We discuss the implications for future research and clinical application. Improvements in immunosuppression have modified short-term survival of deceased-donor allografts, but not their rate of long-term failure. Mismatches between donor and recipient HLA play an important role in the acute and chronic allogeneic immune response against the graft. Perfect matching at clinically relevant HLA loci does not obviate the need for immunosuppression, suggesting that additional genetic variation plays a critical role in both short- and long-term graft outcomes. By combining patient data and samples from supranational cohorts across the United Kingdom and European Union, we performed the first large-scale genome-wide association study analyzing both donor and recipient DNA in 2094 complete renal transplant-pairs with replication in 5866 complete pairs. We studied deceased-donor grafts allocated on the basis of preferential HLA matching, which provided some control for HLA genetic effects. No strong donor or recipient genetic effects contributing to long- or short-term allograft survival were found outside the HLA region. We discuss the implications for future research and clinical application.