The CTLA-4 x OX40 bispecific antibody ATOR-1015 induces anti-tumor effects through tumor-directed immune activation

Anne Månsson Kvarnhammar1, Niina Veitonmäki2, Karin Hägerbrand2

  • 1Alligator Bioscience AB, Medicon Village, Scheelevägen 2, 223 81, Lund, Sweden. amk@alligatorbioscience.com.

Abstract

Insights

ATOR-1015, a novel bispecific antibody, activates T-cells and depletes regulatory T-cells to combat cancer. This new therapy shows promise for improved efficacy and reduced toxicity in cancer treatment.

Area of Science:

  • Immunology
  • Oncology
  • Cancer Immunotherapy

Background:

  • Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) blocking antibodies like ipilimumab show durable effects in melanoma.
  • Current CTLA-4 therapies have potential but may be limited by toxicities, necessitating improved treatments.
  • There is a need for novel CTLA-4 targeting therapies with a better benefit-risk profile.

Purpose of the Study:

  • To evaluate ATOR-1015, a bispecific antibody targeting CTLA-4 and OX40, for its potential as a next-generation cancer immunotherapy.
  • To assess the in vitro and in vivo efficacy of ATOR-1015 in activating T-cells, depleting regulatory T-cells, and mediating anti-tumor responses.
  • To investigate the potential of ATOR-1015 to enhance responses to PD-1 inhibition and establish long-term immunological memory.

Main Methods:

  • ATOR-1015, a CTLA-4 x OX40 bispecific antibody, was engineered.
  • In vitro studies involved T-cell activation and regulatory T-cell (Treg) depletion assays using human cells.
  • In vivo anti-tumor efficacy was assessed in syngeneic mouse tumor models, with analysis of immune cell populations and activation markers.

Main Results:

  • ATOR-1015 demonstrated in vitro T-cell activation and Treg depletion.
  • Treatment with ATOR-1015 reduced tumor growth and improved survival in bladder, colon, and pancreas cancer models.
  • ATOR-1015 induced tumor-specific immunological memory, enhanced anti-PD-1 response, and localized to tumors, reducing Tregs while increasing CD8+ T cells.

Conclusions:

  • ATOR-1015 simultaneously targets CTLA-4 and OX40, enhancing immune activation within the tumor microenvironment.
  • This bispecific antibody offers potential as a next-generation CTLA-4 therapy with improved efficacy and reduced toxicity.
  • ATOR-1015 is expected to synergize with anti-PD-1/PD-L1 therapies, with clinical development initiated.

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