BIO Integration · 2024 · 17 citations · 80 references
MedicineImmunologyOncologyCancer ImmunologyImmunotherapyTumor ImmunologyCancer ImmunotherapyImmune Checkpoint RegulationTumor Immune MicroenvironmentTumor Microenvironment ModulationTumor-associated AntigensTumor-associated MacrophagesCancer Immunotherapy NanoparticlesImmune Checkpoint DysregulationImmune Checkpoint EvasionImmune Escape From Tumor AntigensLectin-glycan Interactions In CancerTumor Antigen-based ImmunotherapyTumor-associated Antigen TargetingTumor-associated Glycoproteins
Abstract CD24, also known as heat-stable protein, is a highly glycosylated glycosylphosphatidylinositol junction membrane protein. CD24 specifically binds sialic-acid-binding Ig-like lectin 10 (Siglec10) on macrophages and serves as a “don’t eat me” signal, thus blocking the phagocytosis of tumor cells by macrophages and triggering tumor immune escape. Blocking the CD24-Siglec10 axis to reprogram the tumor immune microenvironment is a current research hotspot in cancer immunotherapy. Targeting the CD24-Siglec10 axis has received widespread attention, because of the high expression of CD24 on a variety of tumor cells and absence of blood toxicity. Targeting the CD24-Siglec10 axis as a cancer immunotherapy has shown favorable results and progress in preclinical studies. In this review, we summarize the discovery and functions of the CD24-Siglec10 axis, and review the roles and effects of this axis as a novel immune checkpoint in cancer immunotherapy. We also highlight recent advances in nanoparticle-mediated treatments targeting the CD24-Siglec10 axis for enhancing cancer immunotherapy.
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