Removal of anti-A and anti-B blood group antibodies from human blood has be
en shown to facilitate cross-matched kidney transplantation by preventing h
yperacute rejection. Patients in these studies had anti-A and anti-B antibo
dies removed by using plasmapheresis, followed by immunoadsorption onto pac
ked bead columns. We conducted a study to assess the feasibility of selecti
vely removing anti-A and anti-B antibodies directly from blood by using mod
ified dialysis filters. An anti-A and anti-B specific antigen was covalentl
y attached to the lumenal surfaces of hollow fibers within selected commerc
ial dialysis modules. The filters were able to reduce the anti-A and anti-B
titers of 300 ml of blood to 2 or below low molecular weight fraction of o
ur antigen system was found to have no antibody binding capacity. The stand
ard antigen was purified by removal of the low molecular weight fraction an
d a dialysis filter was modified by using the purified:antigen. This filter
displayed a six-fold higher capacity than a dialysis filter modified with
the same mass of standard antigen. We conclude that selective blood group a
ntibody removal by antigen modified dialysis filters is feasible and may be
a simpler system than plasmapheresis followed by immunoadsorption.