Effect of seven new vasoactive immunoconjugates on the enhancement of monoclonal antibody uptake in tumors
- 1 February 1994
- Vol. 73 (S3) , 824-831
- https://doi.org/10.1002/1097-0142(19940201)73:3+<824::aid-cncr2820731312>3.0.co;2-v
Abstract
To enhance monoclonal antibody uptake in tumors, seven novel vasoactive immunoconjugates were developed that selectively alter the vascular permeability and/or blood volume of tumors in vivo. These immunoconjugates, composed of IL-1 beta, IL-2, TNF-alpha, physalaemin, leukotriene B4, histamine, and bradykinin chemically linked to TNT-1, a murine monoclonal antibody that binds necrotic regions in tumors, have been tested for their effects on antibody uptake in vivo. Groups of four mice, each bearing the ME-180 human cervical carcinoma, were pretreated either 3 or 24 hours before the administration of I-125 labeled TNT-1 F(ab')2 fragment. Three-day biodistribution studies then were performed to determine the amount of radiolabeled antibody in the tumors and normal organs of the mice. In addition, mechanism of action studies were performed to determine if the vasoactive immunoconjugate affected the vascular permeability or blood volume of the tumor vessels. TNT-1/IL-2 gave the highest percent injected dose/g in tumor (4.80), compared with TNT-1/TNF (4.00), TNT-1/IL-1 (3.83), TNT-1/leukotriene-B4 (2.84), TNT-1/histamine (2.80), TNT-1/physalaemin (2.19), TNT-1/bradykinin (1.57), or TNT-1 alone (1.28). All of these immunoconjugates showed specific enhancement of monoclonal antibody uptake in tumor with no changes seen in normal tissues. Quantitative studies that demonstrated the mechanism of action of these immunoconjugates showed that TNT-1/IL-2 and TNT-1/histamine produced a marked change in the vasopermeability of tumor vessels but had no effect on tumor blood volume. In contrast, TNT-1/IL-1 and TNT-1/TNF produced a combination of effects, and TNT-1/leukotriene B4, TNT-1/bradykinin, and TNT-1/physalaemin affected only tumor blood volume. These studies indicate that pretreatment with vasoactive immunoconjugates may improve monoclonal antibody uptake in tumors significantly and thereby increase the therapeutic index of monoclonal antibody-directed immunotherapy.Keywords
This publication has 27 references indexed in Scilit:
- Complement research: biosynthesis, genetics, immunoregulatory role and clinical studiesImmunology Today, 1992
- Tumour Necrosis Factor‐α Induces Neutrophil‐Mediated Injury of Cultured Human Endothelial CellsScandinavian Journal of Immunology, 1991
- Interleukin-1 and interleukin-1 antagonismBlood, 1991
- Tumor necrosis factor enhances the neutrophil‐dependent increase in endothelial permeabilityJournal of Cellular Physiology, 1990
- Multiple-Drug Resistance in Human CancerNew England Journal of Medicine, 1987
- Recombinant Human Tumor Necrosis Factor-α: Effects on Proliferation of Normal and Transformed Cells in VitroScience, 1985
- The Numerous Postulated Biological Manifestations of Interleukin-1Journal of Leukocyte Biology, 1984
- Physalaemin: An Amphibian Tachykinin in Human Lung Small-Cell CarcinomaScience, 1983
- On the Mechanism of Vascular Leakage Caused by Histamine-Type MediatorsCirculation Research, 1967
- STUDIES ON INFLAMMATIONThe Journal of cell biology, 1961