A. Ishikawa et al., EXPERIENCE OF ABO-INCOMPATIBLE LIVING KIDNEY-TRANSPLANTATION AFTER DOUBLE FILTRATION PLASMAPHERESIS, Clinical transplantation, 12(2), 1998, pp. 80-83
We achieved success in ABO-incompatible renal allografting after remov
ing anti-A and/or anti-B antibodies from the recipient's plasma using
double filtration plasmapheresis (DFPP). We report here the results of
our initial 2 cases. Case 1 was a 40-yr-old female whose blood group
was A +. The donor was her younger brother, a 37-yr-old male, whose bl
ood group was B +. The human lymphocyte antigens (HLAs) were one haplo
type identical, and the stimulation index of the mixed lymphocyte cult
ure (MLC-SI) was 34. Case 2 was a 28-yr-old male whose blood group was
B +. The donor was his father, a 58-yr-old male, whose blood group wa
s AB +. The HLAs were one-haplotype identical as well, and the MLC-SI
was 71. We carried out 4 sessions of DFPP pre-operatively; i.e. on day
s -6, -4, -2 and -1. 2.51 of plasma were treated with 500 ml of 4.4% p
lasma protein fraction in each procedure. The pre-operative target tit
er of anti-A/B antibody, measured by the saline tube test, was set at
less than x 8. We also used 5 kinds of immunosuppressants. Cyclosporin
e was administered on day -2 beginning with 8 mg/kg/d, and its dose wa
s modified according to the trough level. 500 mg of methylprednisolone
were administered intravenously during the operation, and prednisolon
e was started on day 1 with 60 mg/d and tapered. Azathioprine was star
ted on day -2 with 2 mg/kg/d for 7 d and 1 mg/kg/d thereafter. 5 mg/kg
/d of gusperimus was given intravenously from day 0 for 5 d. 30 mg/kg/
d of ALG was given intravenously from day 0 for 14 d. Along with these
immunosuppressants, 0.1 mg/kg/h of nafamostat mesilate was administer
ed intravenously from day 0 for 3 d, and 4 mg/kg/d of ticlopidine was
given orally from day 3. X-Ray irradiation to the renal graft was not
done. Following splenectomy standard renal allografting was performed.
In Case 1, the titer of anti-B antibody was reduced from x 16 to x 4.
In Case 2, the titer of anti-A antibody was reduced from x 32 to x 4.
The post-operative courses of these 2 cases were satisfactory. Althou
gh our experience is limited, ABO incompatible kidney transplantation
can safely be performed using DFPP.