bioRxivCancer BiologyPreprint
Bifunctional Phagocytic Synapse Enhancers for Cancer Immunotherapy
Valerio SabatinoiD, Silvan FleischiD, Cong TangiD, Felix Müller, Carlos Labão‐AlmeidaiD, Wei Ting KhawiD, Sabrina A. HoganiD, Derrick R. HicksiD, Márcia FontesiD, Ana Raquel CoelhoiD, Wei YangiD, Irene SarkariD, Debarati ShomeiD, Aldrin V. VascoiD, Mar Cabeza-CabrerizoiD, Theresa V. RohmiD, Rogier M. ReijmersiD, Deniz KaymakiD, Fiona GersteriD, David A. BakeriD, Rita FioriD, Gregor HütteriD, Gonçalo J. L. BernardesiD
Abstract
Immunotherapy profoundly impacted cancer treatments by harnessing the patients immune system. Phagocytosis, the process whereby immune cells engulf and destroy foreign particles or cells, plays a critical role in tumour cell clearance. Herein, we introduce a novel concept termed "ENPHASYS" - Enhancement of Phagocytic Synapses - designed to direct and amplify phagocytosis of cancer cells using heterobifunctional molecules named phagocytic synapse enhancers (PSEs). By engineering a de novo PD-L1 binder linked to a natural phagocytosis promoting peptide, tuftsin, the resulting PSE combines PD-L1 blockade with enhanced tumour cell phagocytosis; in addition, the PSEs induce macrophages to internalize a membrane or extracellular target. Intratumoural treatment of colorectal carcinoma- or glioblastoma-burdened immunocompetent animals resulted in beneficial overall survival, delayed tumour growth and a potent antitumor response driven by T-cell activation and TAM reprogramming, underpinning the translational relevance of ENPHASYS. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=118 SRC="FIGDIR/small/642658v1_ufig1.gif" ALT="Figure 1"> View larger version (19K): org.highwire.dtl.DTLVardef@1673fd4org.highwire.dtl.DTLVardef@18fa319org.highwire.dtl.DTLVardef@11cf680org.highwire.dtl.DTLVardef@7b8784_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: mouse
- research focus: cancer & tumor microenvironment
- research focus: host-pathogen & immune response
- research focus: cell signaling & trafficking
- research focus: drug response / drug discovery
- approach: experimental assay
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Macrophage Activation by a Substituted PyrimidoIndole Increases Anti-Cancer Activity
J. Hardie, J. A. Mas-Rosario, … M. E. Farkas·bioRxiv·Mar 18, 2019
- Chimeric antigen receptors that trigger phagocytosis
M. A. Morrissey, A. P. Williamson, … R. D. Vale·bioRxiv·May 16, 2018
- Selective Display of a Chemoattractant Agonist on Cancer Cells Activates the Formyl Peptide Receptor 1 on Immune Cells
E. L. Sikorski, J. Wehr, … D. Thevenin·bioRxiv·Sep 27, 2021
- Cooperative phagocytosis underlies macrophage immunotherapy of solid tumours and initiates a broad anti-tumour IgG response
J. C. Andrechak, L. J. Dooling, … D. E. Discher·bioRxiv·Jan 1, 2022
- Exclusion of PD-1 from the immune synapse: a novel strategy to modulate T cell function
- Engineering a PD-L1-sensing synthetic receptor for programmable macrophage-mediated phagocytosis
Ilaria De Martino, Luigi Russo, … Velia Siciliano·bioRxiv·Jan 21, 2026