A new anti-idiotype antibody capable of binding rituximab on the surface of lymphoma cells

  • Mark S. Cragg
  • , Mike B. Bayne
  • , Alison L. Tutt
  • , Ruth R. French
  • , Stephen Beers
  • , Martin J. Glennie
  • , Timothy M. Illidge

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The chimeric anti-CD20 monoclonal antibody (mAb), rituximab, is an established part of the management of many non-Hodgkin lymphomas. The in vivo action of rituximab remains elusive, and this partially reflects a lack of highly specific reagents to detect rituximab binding at the cell surface. Here we report a new high-affinity mAb (MB2A4) with fine specificity for the idiotype of rituximab. It is able to detect rituximab in vitro, in the presence of high levels of human immunoglobulin G (IgG), in the serum of patients receiving rituximab therapy, and, surprisingly, when rituximab is bound to CD20 on the cell surface. We propose that the anti-idiotype (Id) binds to rituximab molecules bound univalently at the cell surface, facilitated by the relatively high off-rate of rituximab. This reagent provides new insights into the binding of rituximab at the cell surface and demonstrates a mode of binding that could be exploited for the surface detection of other mAbs with clinical and biologic applications. © 2004 by The American Society of Hematology.
    Original languageEnglish
    Pages (from-to)2540-2542
    Number of pages2
    JournalBlood
    Volume104
    Issue number8
    DOIs
    Publication statusPublished - 15 Oct 2004

    Keywords

    • Animals
    • immunology: Antibodies, Anti-Idiotypic
    • blood: Antibodies, Monoclonal
    • immunology: Antigens, CD20
    • immunology: B-Lymphocytes
    • Cell Line, Tumor
    • metabolism: Cell Membrane
    • Humans
    • Immunotherapy
    • drug therapy: Lymphoma, B-Cell
    • Rats
    • Research Support, Non-U.S. Gov't

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