Abstract
Soon after their discovery (1), monoclonal antibodies (MAbs) were exploited for their targeting specificity to deliver cytotoxic moieties, such as protein toxins, enzymes that activate prodrugs in situ, chemotherapeutic agents, and radionuclides. Many of this first-class generation of protein-protein conjugates, presented chemists with the challenge of designing a linker that is easily cleaved intracellularly but sufficiently stable in the blood circulation, and of developing purification procedures for obtaining highly active preparations suitable for clinical trials.
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Canevari, S., Colnaghi, M.I., Cattel, L., Dosio, F. (2002). Antibody-Toxin Conjugates. In: Pagé, M. (eds) Tumor Targeting in Cancer Therapy. Cancer Drug Discovery and Development. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-167-1_15
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DOI: https://doi.org/10.1007/978-1-59259-167-1_15
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