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1 al inactive disease in patients treated with anti-idiotype antibodies.
2 were treated with 52 courses of custom-made anti-idiotype antibodies.
4 s studies suggested that vaccination with an anti-idiotype antibody 3H1, which mimics a specific epit
5 rcinoembryonic antigen (CEA), and that of an anti-idiotype antibody, 3H1, which mimics CEA and can be
6 proach that is analogous to the isolation of anti-idiotype antibodies and were able to isolate peptid
7 se unconfirmed (CR/CRu) to CVP and making an anti-idiotype antibody are 2 independent factors that ea
10 characterize the structural footprint of an anti-idiotype antibody (E1) specific for a potent, fully
15 data demonstrate the utility of employing an anti-idiotype antibody to monitor a patient's specific i
16 ound to inhibit mAb HGAC 39.G3 binding to an anti-idiotype antibody with approximately 1000-fold grea
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