A PSMA-Targeting CD3 Bispecific Antibody Induces Antitumor Responses that Are Enhanced by 4-1BB Costimulation

Cancer Immunol Res. 2020 May;8(5):596-608. doi: 10.1158/2326-6066.CIR-19-0518. Epub 2020 Mar 17.

Abstract

Patients with hematologic cancers have improved outcomes after treatment with bispecific antibodies that bind to CD3 on T cells and that redirect T cells toward cancer cells. However, clinical benefit against solid tumors remains to be shown. We made a bispecific antibody that targets both the common prostate tumor-specific antigen PSMA and CD3 (PMSAxCD3) and provide evidence for tumor inhibition in several preclinical solid tumor models. Mice expressing the human extracellular regions of CD3 and PSMA were generated to examine antitumor efficacy in the presence of an intact immune system and PSMA expression in normal tissues. PSMAxCD3 accumulated in PSMA-expressing tissues and tumors as detected by immuno-PET imaging. Although PSMAxCD3 induced T-cell activation and showed antitumor efficacy in mice with low tumor burden, PSMAxCD3 lost efficacy against larger solid tumors, mirroring the difficulty of treating solid tumors in the clinic. Costimulatory receptors can enhance T-cell responses. We show here that costimulation can enhance the antitumor efficacy of PSMAxCD3. In particular, 4-1BB stimulation in combination with PSMAxCD3 enhanced T-cell activation and proliferation, boosted efficacy against larger tumors, and induced T-cell memory, leading to durable antitumor responses. The combination of CD3 bispecific antibodies and anti-4-1BB costimulation represents a therapeutic approach for the treatment of solid tumors.

MeSH terms

  • Animals
  • Antibodies, Bispecific / immunology
  • Antibodies, Bispecific / pharmacology*
  • Antibodies, Monoclonal / pharmacology*
  • Antigens, Surface / immunology
  • Antigens, Surface / metabolism
  • CD3 Complex / immunology*
  • CD3 Complex / metabolism
  • Cell Line, Tumor
  • Disease Models, Animal
  • Glutamate Carboxypeptidase II / antagonists & inhibitors*
  • Glutamate Carboxypeptidase II / immunology
  • Glutamate Carboxypeptidase II / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Mice, Transgenic
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / immunology
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology
  • Radioisotopes / pharmacokinetics
  • Radiopharmaceuticals / pharmacokinetics
  • T-Lymphocytes / immunology*
  • Tissue Distribution
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / immunology*
  • Tumor Necrosis Factor Receptor Superfamily, Member 9 / metabolism
  • Zirconium / pharmacokinetics

Substances

  • Antibodies, Bispecific
  • Antibodies, Monoclonal
  • Antigens, Surface
  • CD3 Complex
  • Radioisotopes
  • Radiopharmaceuticals
  • Tumor Necrosis Factor Receptor Superfamily, Member 9
  • Zirconium
  • FOLH1 protein, human
  • Glutamate Carboxypeptidase II
  • Zirconium-89