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The Journal of Nuclear Medicine Vol. 26 No. 5 493-502
© 1985 by Society of Nuclear Medicine
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Chelate Conjugates of Monoclonal Antibodies for Imaging Lymphoid Structures in the Mouse

David A. Goodwin , Claude F. Meares, Michael J. McCall, Michael K. Haseman, Maureen McTigue, Carol I. Diamanti and Warak Chaovapong

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 ({alpha}) IAk MoAb with purified, no-carrier-added 111ln citrate. Labeling efficiency was 85–95%, and the labeled {alpha}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{alpha}lAk MoAb was compared in mice, two IAk positive and one IAk negative strains, and to 125l{alpha}lAk MoAb in one IAk positive strain. The 111ln{alpha}lAk MoAb was more stable in vivo compared to 125l{alpha}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{alpha} 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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Copyright © 1985 by the Society of Nuclear Medicine.