TY - JOUR
T1 - Enzyme-linked immunosorbent assay spot detection of interferon-γ and interleukin 5-producing cells as predictive marker for renal allograft failure
AU - Tary-Lehmann, Magdalena
AU - Hricik, Donald E.
AU - Justice, Amy C.
AU - Potter, Nicholas S.
AU - Heeger, Peter S.
PY - 1998/7/27
Y1 - 1998/7/27
N2 - Background. Despite improvements in the short-term survival of renal transplants, many allografts fail over the 5-10 years after transplantation. We sought to identify an immunologic assay that could identify those patients at high risk for future allograft failure. Methods. Blood samples were obtained from 23 renal allograft recipients with acute and/or chronic graft dysfunction and from 22 controls. Isolated peripheral blood lymphocytes (PBLs) were tested for interferon (IFN)-γ and interleukin (IL)-5 production using an enzyme-linked immunosorbent spot assay. IFN-γIL-5 ratios were calculated and compared between groups. Among the 23 patients with graft dysfunction, the ratios were also compared with graft function at 6 months. Results. IFN-γIL-5 ratios of ≤15 were associated with allograft rejection episodes in 8 of 12 cases, whereas 10 of 11 episodes of graft dysfunction from other causes (infection, drug toxicity, obstruction) were associated with values <15. All normal controls had values <15 (22/22). Among the graft recipients with acute renal failure, all patients with IFN-γIL-5 ratios <15 exhibited improved renal function at 6-month follow-up (14/14), whereas 8 of 9 patients with IFN-γIL-5 ratios ≤15 developed allograft failure at 6 months (sensitivity 100%, specificity 93.3%). Conclusion. In renal transplant recipients with acute allograft dysfunction, mitogen-induced peripheral blood lymphocyte IFN-γIL-5 ratios ≤15 were highly predictive of allograft failure within 6 months of the assay. This test may be a useful prognostic marker for identification of transplant recipients with acute graft dysfunction who are at high risk for future graft loss and thus allow targeted therapeutic interventions to prolong graft survival.
AB - Background. Despite improvements in the short-term survival of renal transplants, many allografts fail over the 5-10 years after transplantation. We sought to identify an immunologic assay that could identify those patients at high risk for future allograft failure. Methods. Blood samples were obtained from 23 renal allograft recipients with acute and/or chronic graft dysfunction and from 22 controls. Isolated peripheral blood lymphocytes (PBLs) were tested for interferon (IFN)-γ and interleukin (IL)-5 production using an enzyme-linked immunosorbent spot assay. IFN-γIL-5 ratios were calculated and compared between groups. Among the 23 patients with graft dysfunction, the ratios were also compared with graft function at 6 months. Results. IFN-γIL-5 ratios of ≤15 were associated with allograft rejection episodes in 8 of 12 cases, whereas 10 of 11 episodes of graft dysfunction from other causes (infection, drug toxicity, obstruction) were associated with values <15. All normal controls had values <15 (22/22). Among the graft recipients with acute renal failure, all patients with IFN-γIL-5 ratios <15 exhibited improved renal function at 6-month follow-up (14/14), whereas 8 of 9 patients with IFN-γIL-5 ratios ≤15 developed allograft failure at 6 months (sensitivity 100%, specificity 93.3%). Conclusion. In renal transplant recipients with acute allograft dysfunction, mitogen-induced peripheral blood lymphocyte IFN-γIL-5 ratios ≤15 were highly predictive of allograft failure within 6 months of the assay. This test may be a useful prognostic marker for identification of transplant recipients with acute graft dysfunction who are at high risk for future graft loss and thus allow targeted therapeutic interventions to prolong graft survival.
UR - http://www.scopus.com/inward/record.url?scp=0032558139&partnerID=8YFLogxK
U2 - 10.1097/00007890-199807270-00014
DO - 10.1097/00007890-199807270-00014
M3 - Article
C2 - 9701268
AN - SCOPUS:0032558139
SN - 0041-1337
VL - 66
SP - 219
EP - 224
JO - Transplantation
JF - Transplantation
IS - 2
ER -