TY - JOUR
T1 - Peripheral eosinophil count both before and after liver transplantation predicts acute cellular rejection
AU - Dollinger, M. M.
AU - Plevris, J. N.
AU - Bouchier, I. A.D.
AU - Harrison, D. J.
AU - Hayes, P. C.
PY - 1997
Y1 - 1997
N2 - Acute cellular rejection is common after orthotopic liver transplantation and an important cause of graft dysfunction. Eosinophils, potent mediators of tissue damage, have been implicated in the pathogenesis of acute rejection. We studied 55 patients, all of whom had a protocol biopsy 7 days after transplantation and whose peripheral eosinophil count was monitored daily for 11 days after transplantation. Patients were divided clinicopathologically into two groups: group A, without rejection, group B, with rejection. Group B (36% of patients) developed rejection within the 11- day study period. The pretransplant eosinophil count was significantly higher in group B, compared with group A (0.31 ± 0.08 v 0.10 ± 0.01 (x109/L), p <. 001). After transplantation, the eosinophil count fell to low levels in both groups. By day 3 there was a statistically significant rise in the eosinophil count in group B compared with group A, with a maximum at day 7 [0.51 ± 0.06 v 0.26 ± 0.03 (x109/L) p < .001]. After treatment with steroids, the eosinophil count dropped to values similar to those in group A and remained low thereafter in 16 of 20 patients. Four patients had a second episode of rejection; in each of these, eosinophils were raised again and decreased with resolution of the rejection. An eosinophil count threshold of 0.13 (x109/L) before transplantation and 0.33 (x109/L) on day 7 after transplantation predicted the development of rejection (sensitivity 72/70%, specificity 66/63%, negative predictive value 82/79%). We conclude that a raised eosinophil count is associated with acute rejection. The raised eosinophil count before transplantation in group B suggests that these patients are predisposed to acute rejection, and earlier intervention may be indicated.
AB - Acute cellular rejection is common after orthotopic liver transplantation and an important cause of graft dysfunction. Eosinophils, potent mediators of tissue damage, have been implicated in the pathogenesis of acute rejection. We studied 55 patients, all of whom had a protocol biopsy 7 days after transplantation and whose peripheral eosinophil count was monitored daily for 11 days after transplantation. Patients were divided clinicopathologically into two groups: group A, without rejection, group B, with rejection. Group B (36% of patients) developed rejection within the 11- day study period. The pretransplant eosinophil count was significantly higher in group B, compared with group A (0.31 ± 0.08 v 0.10 ± 0.01 (x109/L), p <. 001). After transplantation, the eosinophil count fell to low levels in both groups. By day 3 there was a statistically significant rise in the eosinophil count in group B compared with group A, with a maximum at day 7 [0.51 ± 0.06 v 0.26 ± 0.03 (x109/L) p < .001]. After treatment with steroids, the eosinophil count dropped to values similar to those in group A and remained low thereafter in 16 of 20 patients. Four patients had a second episode of rejection; in each of these, eosinophils were raised again and decreased with resolution of the rejection. An eosinophil count threshold of 0.13 (x109/L) before transplantation and 0.33 (x109/L) on day 7 after transplantation predicted the development of rejection (sensitivity 72/70%, specificity 66/63%, negative predictive value 82/79%). We conclude that a raised eosinophil count is associated with acute rejection. The raised eosinophil count before transplantation in group B suggests that these patients are predisposed to acute rejection, and earlier intervention may be indicated.
UR - http://www.scopus.com/inward/record.url?scp=0031048605&partnerID=8YFLogxK
U2 - 10.1002/lt.500030203
DO - 10.1002/lt.500030203
M3 - Article
C2 - 9346724
AN - SCOPUS:0031048605
SN - 1074-3022
VL - 3
SP - 112
EP - 117
JO - Liver Transplantation and Surgery
JF - Liver Transplantation and Surgery
IS - 2
ER -