Programming tissue-sensing T cells that deliver therapies to the brain

Science. 2024 Dec 6;386(6726):eadl4237. doi: 10.1126/science.adl4237. Epub 2024 Dec 6.

Abstract

To engineer cells that can specifically target the central nervous system (CNS), we identified extracellular CNS-specific antigens, including components of the CNS extracellular matrix and surface molecules expressed on neurons or glial cells. Synthetic Notch receptors engineered to detect these antigens were used to program T cells to induce the expression of diverse payloads only in the brain. CNS-targeted T cells that induced chimeric antigen receptor expression efficiently cleared primary and secondary brain tumors without harming cross-reactive cells outside of the brain. Conversely, CNS-targeted cells that locally delivered the immunosuppressive cytokine interleukin-10 ameliorated symptoms in a mouse model of neuroinflammation. Tissue-sensing cells represent a strategy for addressing diverse disorders in an anatomically targeted manner.

MeSH terms

  • Animals
  • Brain Diseases* / therapy
  • Brain Neoplasms / immunology
  • Brain Neoplasms / therapy
  • Brain* / immunology
  • Cell Engineering* / methods
  • Encephalomyelitis, Autoimmune, Experimental* / therapy
  • Extracellular Matrix / metabolism
  • Humans
  • Interleukin-10* / metabolism
  • Mice
  • Neuroglia / immunology
  • Neuroglia / metabolism
  • Neuroinflammatory Diseases
  • Neurons / immunology
  • Neurons / metabolism
  • Receptors, Chimeric Antigen* / genetics
  • Receptors, Chimeric Antigen* / immunology
  • Receptors, Notch / metabolism
  • T-Lymphocytes* / immunology

Substances

  • Interleukin-10
  • Receptors, Chimeric Antigen
  • Receptors, Notch