E. Loh et al., ROLE OF PANEL-REACTIVE ANTIBODY CROSS-REACTIVITY IN PREDICTING SURVIVAL AFTER ORTHOTOPIC HEART-TRANSPLANTATION, The Journal of heart and lung transplantation, 13(2), 1994, pp. 194-201
To test the hypothesis that elevated preformed circulating antibody le
vels, as measured by panel-reactive antibody levels, predict survival
after orthotopic heart transplantation, we analyzed 120 consecutive pa
tients undergoing heart transplantation at the Brigham and Women's Hos
pital in a retrospective, chart-review format. Prospective; donor-spec
ific lymphocyte crossmatches were performed in all patients with a pan
el-reactive antibody level of 10% or greater. Both the peak pretranspl
antation panel-reactive antibody level and the panel-reactive antibody
level obtained on the day of transplantation were analyzed with respe
ct to the end points of the number of acute rejection episodes, presen
ce of coronary artery disease, and overall survival after transplantat
ion. Patients with a panel-reactive antibody level on the day of trans
plantation of 25% or greater, despite a negative prospective donor-spe
cific lymphocyte crossmatch, demonstrated a trend toward reduced actua
rial long-term survival compared with patients with panel-reactive ant
ibody values less than 25% (p < 0.05). Panel-reactive antibody levels
were not predictive of the number of acute rejection episodes, early (
< 60 days) versus late (greater-than-or-equal-to 60 days) death, or th
e development of graft coronary artery disease. No episodes of hyperac
ute rejection were observed, even in six patients with a positive retr
ospective donor-specific lymphocyte crossmatch. In conclusion, an elev
ated panel-reactive antibody value of 25% or greater at the time of he
art transplantation may be a risk factor for decreased long-term survi
val. A trend toward an increased risk of death caused by rejection was
also observed. Finally, the absence of any episodes of hyperacute rej
ection in patients with positive retrospective lymphocytotoxic crossma
tches again raises the need to reevaluate the utility of prospective d
onor-specific lymphocyte crossmatches to prevent this complication.