The present and future of bispecific antibodies for cancer therapy

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作者
Christian Klein
Ulrich Brinkmann
Janice M. Reichert
Roland E. Kontermann
机构
[1] Roche Innovation Center Zurich,Roche Pharma Research and Early Development
[2] Roche Innovation Center Munich,Roche Pharma Research and Early Development
[3] The Antibody Society,Institute of Cell Biology and Immunology
[4] University Stuttgart,undefined
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摘要
Bispecific antibodies (bsAbs) enable novel mechanisms of action and/or therapeutic applications that cannot be achieved using conventional IgG-based antibodies. Consequently, development of these molecules has garnered substantial interest in the past decade and, as of the end of 2023, 14 bsAbs have been approved: 11 for the treatment of cancer and 3 for non-oncology indications. bsAbs are available in different formats, address different targets and mediate anticancer function via different molecular mechanisms. Here, we provide an overview of recent developments in the field of bsAbs for cancer therapy. We focus on bsAbs that are approved or in clinical development, including bsAb-mediated dual modulators of signalling pathways, tumour-targeted receptor agonists, bsAb–drug conjugates, bispecific T cell, natural killer cell and innate immune cell engagers, and bispecific checkpoint inhibitors and co-stimulators. Finally, we provide an outlook into next-generation bsAbs in earlier stages of development, including trispecifics, bsAb prodrugs, bsAbs that induce degradation of tumour targets and bsAbs acting as cytokine mimetics.
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页码:301 / 319
页数:18
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