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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.
Background:
The CTLA-4 blocking antibody ipilimumab has demonstrated substantial and durable effects in patients with melanoma. While CTLA-4 therapy, both as monotherapy and in combination with PD-1 targeting therapies, has great potential in many indications, the toxicities of the current treatment regimens may limit their use. Thus, there is a medical need for new CTLA-4 targeting therapies with improved benefit-risk profile.
Methods:
ATOR-1015 is a human CTLA-4 x OX40 targeting IgG1 bispecific antibody generated by linking an optimized version of the Ig-like V-type domain of human CD86, a natural CTLA-4 ligand, to an agonistic OX40 antibody. In vitro evaluation of T-cell activation and T regulatory cell (Treg) depletion was performed using purified cells from healthy human donors or cell lines. In vivo anti-tumor responses were studied using human OX40 transgenic (knock-in) mice with established syngeneic tumors. Tumors and spleens from treated mice were analyzed for CD8+ T cell and Treg frequencies, T-cell activation markers and tumor localization using flow cytometry.
Results:
ATOR-1015 induces T-cell activation and Treg depletion in vitro. Treatment with ATOR-1015 reduces tumor growth and improves survival in several syngeneic tumor models, including bladder, colon and pancreas cancer models. It is further demonstrated that ATOR-1015 induces tumor-specific and long-term immunological memory and enhances the response to PD-1 inhibition. Moreover, ATOR-1015 localizes to the tumor area where it reduces the frequency of Tregs and increases the number and activation of CD8+ T cells.
Conclusions:
By targeting CTLA-4 and OX40 simultaneously, ATOR-1015 is directed to the tumor area where it induces enhanced immune activation, and thus has the potential to be a next generation CTLA-4 targeting therapy with improved clinical efficacy and reduced toxicity. ATOR-1015 is also expected to act synergistically with anti-PD-1/PD-L1 therapy. The pre-clinical data support clinical development of ATOR-1015, and a first-in-human trial has started (NCT03782467).
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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