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Metabolizable111in chelate conjugated anti-idiotype monoclonal antibody for radioimmunodetection of lymphoma in mice

โœ Scribed by Michael K. Haseman; David A. Goodwin; Claude F. Meares; Mark S. Kaminski; Theodore G. Wensel; Michael J. McCall; Ronald Levy


Publisher
Springer
Year
1986
Tongue
English
Weight
577 KB
Volume
12
Category
Article
ISSN
0340-6997

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โœฆ Synopsis


The relative biological properties of 111In-labeled monoclonal antibodies (MoAb) coupled with a conventional bifunctional chelate (BC) and a new, enzyme metabolizable, bifunctional chelate (BCM) were investigated. A rat IgG2a MoAb against idiotype from a mouse B-cell lymphoma was utilized. Mice bearing B-cell lymphomas in the subcutaneous tissues of the flank were given IV-injections of labeled MoAb and imaged or killed for organ counting at 24 h or 48 h. Rat anti-dinitrophenyl IgG2a MoAb and non-specific polyclonal mouse IgG were used as controls. Compared to BC, the use of BCM resulted in a substantial decrease in blood background activity, a shorter biological half-life and an increase in tumor to blood ratio at the expense of a moderate decrease in absolute tumor uptake. The versatile chemistry of these C-1 substituted bifunctional chelates provides a variety of possible enzyme cleavable moieties for further investigation.


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Enhanced clearance of radiolabeled murin
โœ Robert M. Sharkey; Otto C. Boerman; Ana Natale; David Pawlyk; Marc Monestier; Mi ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 945 KB

A syngeneic anti-idiotype monoclonal antibody (MAb) (CM-I I) directed against an anti-carcinoembryonic antigen (CEA) murine MAb (NP-4) was evaluated as a second antibody (SA) to promote the rapid clearance of radiolabeled NP-4 from the blood. Initial studies confirmed that CM-I I IgG removed l3Il-NP