Therapeutic potential of monovalent monoclonal antibodies
- 29 March 1984
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 308 (5958) , 460-462
- https://doi.org/10.1038/308460a0
Abstract
One therapeutic use for monoclonal antibody technology1 is the elimination of categories of unwanted cells by virtue of their distinct cell surface antigens. The efficiency of cell destruction by complement lysis or opsonization depends on a number of factors such as antibody specificity and isotype as well as certain properties of the target antigen2. In some instances cells can escape destruction by redistributing and eventually losing the antigen–antibody complexes from their surface3,4. This process, known as antigenic modulation, generally depends on bivalent antibody binding. Starting from the observation that rabbit antisera can be made more effective at killing tumour cells if they are first rendered univalent by limited proteolysis, we have now prepared a number of monovalent rat monoclonal antibodies to human cell-surface antigens. We find that these antibodies are no longer able to bring about modulation of their target antigens and have an enhanced facility for lysis with human complement. These special properties should greatly increase the therapeutic potential of monoclonal antibodies.Keywords
This publication has 15 references indexed in Scilit:
- The mechanism of synergistic complement‐mediated lysis of rat red cells by monoclonal IgG antibodiesEuropean Journal of Immunology, 1983
- USE OF ANTI-T-CELL MONOCLONAL ANTIBODY OKT3 TO PREVENT ACUTE GRAFT-VERSUS-HOST DISEASE IN ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR ACUTE LEUKAEMIAThe Lancet, 1982
- Univalent antibodies kill tumour cells in vitro and in vivoNature, 1982
- ELIMINATION OF T‐LYMPHOCYTES FROM HUMAN BONE MARROW WITH MONOCLONAL T‐ANTIBODIES AND CYTOLYTIC COMPLEMENTBritish Journal of Haematology, 1982
- Monoclonal Antibodies Specific for Rat IgG1, IgG2a, and IgG2b Subclasses, and Kappa Chain Monotypic and Allotypic Determinants: Reagents for Use with Rat Monoclonal AntibodiesHybridoma, 1982
- Anti‐D‐coated Rh‐positive red cells will bind the first component of the complement pathway, C1qFEBS Letters, 1981
- Differences in the ability of rat IgG subclasses to consume complement in homologous and heterologous serumImmunology Letters, 1980
- Rat × rat hybrid myelomas and a monoclonal anti-Fd portion of mouse IgGNature, 1979
- Continuous cultures of fused cells secreting antibody of predefined specificityNature, 1975
- SOME ASPECTS OF NORMAL AND ABNORMAL CELL SURFACE GENETICSAnnual Review of Genetics, 1969