TY - JOUR
T1 - Bridging the gap with multispecific immune cell engagers in cancer and infectious diseases
AU - Rolin, Camille
AU - Zimmer, Jacques
AU - Seguin-Devaux, Carole
N1 - Funding
CR is supported by a grant from the National Research Fund Luxembourg (FNR), Doctoral Training Unit “i2TRON”, PRIDE19/14254520, project 20200831.
© 2024. The Author(s).
PY - 2024/7
Y1 - 2024/7
N2 - 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.
AB - 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.
KW - Cancer
KW - Immune cell engagers
KW - Immunotherapy
KW - Multispecific antibodies
KW - Virus
UR - http://www.scopus.com/inward/record.url?scp=85194280022&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/38789528
U2 - 10.1038/s41423-024-01176-4
DO - 10.1038/s41423-024-01176-4
M3 - Review article
C2 - 38789528
SN - 1672-7681
VL - 21
SP - 643
EP - 661
JO - Cellular and Molecular Immunology
JF - Cellular and Molecular Immunology
IS - 7
ER -