Bioengineering T cells to target carbohydrate to treat opportunistic fungal infection

Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):10660-5. doi: 10.1073/pnas.1312789111. Epub 2014 Jul 7.

Abstract

Clinical-grade T cells are genetically modified ex vivo to express chimeric antigen receptors (CARs) to redirect their specificity to target tumor-associated antigens in vivo. We now have developed this molecular strategy to render cytotoxic T cells specific for fungi. We adapted the pattern-recognition receptor Dectin-1 to activate T cells via chimeric CD28 and CD3-ζ (designated "D-CAR") upon binding with carbohydrate in the cell wall of Aspergillus germlings. T cells genetically modified with the Sleeping Beauty system to express D-CAR stably were propagated selectively on artificial activating and propagating cells using an approach similar to that approved by the Food and Drug Administration for manufacturing CD19-specific CAR(+) T cells for clinical trials. The D-CAR(+) T cells exhibited specificity for β-glucan which led to damage and inhibition of hyphal growth of Aspergillus in vitro and in vivo. Treatment of D-CAR(+) T cells with steroids did not compromise antifungal activity significantly. These data support the targeting of carbohydrate antigens by CAR(+) T cells and provide a clinically appealing strategy to enhance immunity for opportunistic fungal infections using T-cell gene therapy.

Keywords: T-cell therapy; adoptive immunotherapy; fungus; β-1,3-glucan.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antigens, CD19 / metabolism
  • Aspergillosis / immunology*
  • Aspergillosis / microbiology
  • Aspergillosis / pathology
  • Aspergillosis / therapy*
  • Aspergillus / drug effects
  • Aspergillus / physiology
  • Bioengineering / methods*
  • Carbohydrates / antagonists & inhibitors*
  • Dexamethasone / pharmacology
  • Humans
  • Hyphae / drug effects
  • Hyphae / physiology
  • Immunophenotyping
  • Lectins, C-Type / metabolism
  • Lymphocyte Activation / drug effects
  • Mice
  • Opportunistic Infections / immunology*
  • Opportunistic Infections / pathology
  • Opportunistic Infections / therapy*
  • Receptors, Antigen, T-Cell / metabolism
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology*

Substances

  • Antigens, CD19
  • Carbohydrates
  • Lectins, C-Type
  • Receptors, Antigen, T-Cell
  • dectin 1
  • Dexamethasone