Basiliximab is a chimeric monoclonal antibody directed against the alpha ch
ain of interleukin-2 (IL-2) receptors, Given its expected volume of distrib
ution (plasma volume), therapeutic plasmapheresis may be expected to lower
serum Basiliximab levels. A 20 mg dose of Basiliximab was given before plas
mapheresis, Blood and pheresis fluid samples were obtained to monitor Basil
iximab levels. A total of three blood samples were drawn: the first was obt
ained 4 hours before, the second sample immediately before commencement, an
d the third 2 hours after cessation of plasmapheresis. A fourth sample was
obtained from the removed plasma. There was an appreciable reduction in Bas
iliximab concentration levels after plasmapheresis, From the change in seru
m concentration after plasmapheresis, approximately 64.6% of circulating Ba
siliximab was removed. Plasmapheresis removes substantial amounts of Basili
ximab. Therefore, supplemental Basiliximab should be given after plasmapher
esis to maintain the desired duration of IL-2R saturation. (C) 2001 by the
National Kidney Foundation, Inc.