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Removal of basiliximab by plasmapheresis.

  • C. N. Okechukwu
  • , H. U. Meier-Kriesche
  • , D. Armstrong
  • , D. Campbell
  • , C. Gerbeau
  • , B. Kaplan

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Basiliximab is a chimeric monoclonal antibody directed against the alpha chain of interleukin-2 (IL-2) receptors. Given its expected volume of distribution (plasma volume), therapeutic plasmapheresis may be expected to lower serum Basiliximab levels. A 20-mg dose of Basiliximab was given before plasmapheresis. Blood and pheresis fluid samples were obtained to monitor Basiliximab levels. A total of three blood samples were drawn: the first was obtained 4 hours before, the second sample immediately before commencement, and the third 2 hours after cessation of plasmapheresis. A fourth sample was obtained from the removed plasma. There was an appreciable reduction in Basiliximab concentration levels after plasmapheresis. From the change in serum concentration after plasmapheresis, approximately 64.6% of circulating Basiliximab was removed. Plasmapheresis removes substantial amounts of Basiliximab. Therefore, supplemental Basiliximab should be given after plasmapheresis to maintain the desired duration of IL-2R saturation.

    Original languageEnglish (US)
    Pages (from-to)E11
    JournalAmerican journal of kidney diseases : the official journal of the National Kidney Foundation
    Volume37
    Issue number1
    DOIs
    StatePublished - Jan 2001

    ASJC Scopus subject areas

    • Nephrology

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