The effect of serum from orthotopic liver retransplanted rats (re-OLT
serum) on graft-versus-host disease (GVHD) was studied in rats. In the
re-transplantation model of rat liver, orthotopic liver transplantati
on (OLT) was carried out in the DA (RT1(a)) into PVG (RT1(c)) combinat
ion; two days later the DA liver was removed and a new PVG liver impla
nted into the same recipient (re-OLT). In the in vivo GVHD model, male
PVG rats were sublethally irradiated and injected intravenously with
3 x 10(8) DA or BN (RT1(n)) spleen cells through the penial vein. With
in 1 h of the inoculation, rats of the experimental group were injecte
d with 1 mi of re-OLT serum taken at postoperative day (POD) 7. Rats i
n the control group received 1 mi of normal PVG serum or syngeneic re-
OLT serum (PVG-PVG, PVG-PVG). All PVG rats in the control groups died
of GVHD within 21 days after the inoculation of DA or BN spleen lympho
cytes. However, when the animals were treated with re-OLT serum, 100%
(6/6) of the rats survived more than 60 days, following inoculation wi
th DA lymphocytes but not with BN lymphocytes. The POD 7 re-OLT serum
showed a strong inhibition against DA anti-PVG mixed lymphocyte reacti
on (MLR), although re-OLT serum did not contain soluble DA class I ant
igens, anti-DA class I or II antibody. The potential GVHD inhibitory f
actors in re-OLT serum may be two unique immunosuppressive proteins, w
hich have been detected by SDS PAGE and reported previously. We conclu
de that re-OLT serum has immunosuppressive factors, which, at least in
part, prevented the induction of GVHD in rats.