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Nuclear Medicine Service, Veterans Administration Medical Center, Palo Alto; Stanford University School of Medicine, Stanford; and Department of Chemistry, University of California, Davis, California
Correspondence: For reprints contact: David A. Goodwin, MD, VA Medical Center, 3801 Miranda Ave., Palo Alto, CA 94304.
ABSTRACT
Radiolabeling of a mouse monoclonal antibody (MoAb) specific for the mouse histocompatibility alloantigen IAk expressed by the B lymphocytes of BALB/k and C3H mice but not BALB/c mice was performed by mixing the chelate-labeled anti (
) IAk MoAb with purified, no-carrier-added 111ln citrate. Labeling efficiency was 85–95%, and the labeled
IAk MoAb retained its antigen binding properties in vitro and in vivo. The organ, spleen, and lymph node distribution of intravenously and subcutaneously administered 111ln
lAk MoAb was compared in mice, two IAk positive and one IAk negative strains, and to 125l
lAk MoAb in one IAk positive strain. The 111ln
lAk MoAb was more stable in vivo compared to 125l
lAk MoAb, as shown by a much slower excretion and a higher absolute uptake in lymph nodes and spleen. Lymph node to blood ratio was increased twofold by intravenous anti-EDTA MoAb. Subcutaneous injection permitted clear images of the tiny lymph nodes in the mouse. Potential clinical applications of 111ln
lymphocyte MoAb include localization of normal lymph nodes and T & B cell leukemias and lymphomas, as well as detecting lymphatic metastases of other cancers. Therapy may also be possible using MoAbs labeled with beta-emitting metal ions such as yttrium-90.
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