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 language | English |
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Pages (from-to) | 2540-2542 |
Number of pages | 2 |
Journal | Blood |
Volume | 104 |
Issue number | 8 |
DOIs | |
Publication status | Published - 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