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Bridging the gap with multispecific immune cell engagers in cancer and infectious diseases. | LitMetric

Bridging the gap with multispecific immune cell engagers in cancer and infectious diseases.

Cell Mol Immunol

Department of Infection and Immunity, Luxembourg Institute of Health, 29 Rue Henri Koch, L-4354, Esch-Sur-Alzette, Luxembourg.

Published: July 2024

AI Article Synopsis

  • Multispecific antibodies can enhance the effectiveness of immunotherapy by targeting multiple antigens at once, potentially improving treatment outcomes.
  • Immune cell engagers are engineered antibodies that connect immune cells to cancer or infected cells, improving the immune response.
  • The review highlights the current advancements in immune cell engagement, discusses the challenges in applying this knowledge to virology, and suggests future directions for cancer and antiviral therapies.

Article Abstract

By binding to multiple antigens simultaneously, multispecific antibodies are expected to substantially improve both the activity and long-term efficacy of antibody-based immunotherapy. Immune cell engagers, a subclass of antibody-based constructs, consist of engineered structures designed to bridge immune effector cells to their target, thereby redirecting the immune response toward the tumor cells or infected cells. The increasing number of recent clinical trials evaluating immune cell engagers reflects the important role of these molecules in new therapeutic approaches for cancer and infections. In this review, we discuss how different immune cell types (T and natural killer lymphocytes, as well as myeloid cells) can be bound by immune cell engagers in immunotherapy for cancer and infectious diseases. Furthermore, we explore the preclinical and clinical advancements of these constructs, and we discuss the challenges in translating the current knowledge from cancer to the virology field. Finally, we speculate on the promising future directions that immune cell engagers may take in cancer treatment and antiviral therapy.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11214628PMC
http://dx.doi.org/10.1038/s41423-024-01176-4DOI Listing

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