AI Article Synopsis

  • Artificial antigen-presenting cells (aAPCs) made from microgels can effectively activate and expand T cells for cancer therapy by customizing their surface properties.
  • The microgels are coated with charged polymers, which allows for easy attachment of specific stimulatory ligands that enhance T cell activation.
  • By adjusting factors like ligand concentration and microgel stiffness, researchers can control the resulting T cell characteristics and functionality, making this system adaptable for various therapeutic applications.

Article Abstract

Artificial antigen-presenting cells (aAPCs) are currently used to manufacture T cells for adoptive therapy in cancer treatment, but a readily tunable and modular system can enable both rapid T cell expansion and control over T cell phenotype. Here, it is shown that microgels with tailored surface biochemical properties can serve as aAPCs to mediate T cell activation and expansion. Surface functionalization of microgels is achieved via layer-by-layer coating using oppositely charged polymers, forming a thin but dense polymer layer on the surface. This facile and versatile approach is compatible with a variety of coating polymers and allows efficient and flexible surface-specific conjugation of defined peptides or proteins. The authors demonstrate that tethering appropriate stimulatory ligands on the microgel surface efficiently activates T cells for polyclonal and antigen-specific expansion. The expansion, phenotype, and functional outcome of primary mouse and human T cells can be regulated by modulating the concentration, ratio, and distribution of stimulatory ligands presented on microgel surfaces as well as the stiffness and viscoelasticity of the microgels.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11293993PMC
http://dx.doi.org/10.1002/adma.202309860DOI Listing

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