PD-1-CD28 fusion protein strengthens mesothelin-specific TRuC T cells in preclinical solid tumor models

Cell Oncol (Dordr). 2023 Feb;46(1):227-235. doi: 10.1007/s13402-022-00747-9. Epub 2022 Nov 21.

Abstract

Background: T cell receptor fusion constructs (TRuC) consist of an antibody-based single chain variable fragment (scFv) fused to a T cell receptor chain (TCR) and allow recognition of cancer cells in an HLA-independent manner. Unlike chimeric antigen receptors (CAR), TRuC are integrated into the TCR complex resulting in a functional chimera with novel specificity, whilst retaining TCR signaling. To further enhance anti-tumor function, we expressed a PD-1-CD28 fusion receptor in TRuC T cells aiming to prevent tumor-induced immune suppression and T cell anergy.

Methods: The activation level of engineered T cells was investigated in co-culture experiments with tumor cells followed by quantification of released cytokines using ELISA. To study T cell-mediated tumor cell lysis in vitro, impedance-based real-time tumor cell killing and LDH release was measured. Finally, two xenograft mouse cancer models were employed to explore the therapeutic potential of engineered T cells.

Results: In co-culture assays, co-expression of PD-1-CD28 enhanced cytokine production of TRuC T cells. This effect was dependent on PD-L1 to PD-1-CD28 interactions, as blockade of PD-L1 amplified IFN-γ production in unmodified TRuC T cells to a greater level compared to TRuC-PD-1-CD28 T cells. In vivo, PD-1-CD28 co-expression supported the anti-tumor efficacy of TRuC T cells in two xenograft mouse cancer models.

Conclusion: Together, these results demonstrate the therapeutic potential of PD-1-CD28 co-expression in TRuC T cells to prevent PD-L1-induced T cell hypofunction.

Keywords: Adoptive cell transfer; Immunosuppression; PD-1-CD28 fusion protein; T cell hypofunction; TRuC T cells.

MeSH terms

  • Animals
  • B7-H1 Antigen / metabolism
  • CD28 Antigens / metabolism
  • Cell Line, Tumor
  • Humans
  • Mesothelin
  • Mice
  • Neoplasms*
  • Programmed Cell Death 1 Receptor / metabolism
  • Receptors, Antigen, T-Cell / metabolism
  • T-Lymphocytes*

Substances

  • CD28 Antigens
  • Programmed Cell Death 1 Receptor
  • B7-H1 Antigen
  • Mesothelin
  • Receptors, Antigen, T-Cell