TPP-45142-an Anti-HER2 T-cell Engager-Designed for Selective HER2-Low Cancer Immunotherapy

Evelyn De Tavernier1, Peter S Kim2, Eduardo M Bruch3

  • 1NANOBODY Research Platform, Sanofi, Ghent, Belgium.

PubMed

Insights

A novel T cell engager, TPP-45142, effectively targets HER2-low cancers by redirecting T cells. This promising therapy shows potent anti-tumor activity and selectivity, offering hope for patients resistant to current treatments.

Area of Science:

  • Oncology
  • Immunotherapy
  • Molecular Biology

Background:

  • Standard treatments for HER2-positive cancers exist, but HER2-low and trastuzumab-refractory cancers remain a challenge.
  • Trastuzumab and pertuzumab target specific HER2 epitopes, leaving a gap in treatment for certain patient populations.

Purpose of the Study:

  • To develop and evaluate TPP-45142, a novel NANOBODY® domain-based T cell engager (TCE), for targeting HER2-low cancers.
  • To assess the efficacy and safety of TPP-45142 in preclinical models of HER2-low breast, gastric, and gastroesophageal junction adenocarcinoma.

Main Methods:

  • Development of TPP-45142, a TCE utilizing a NANOBODY® domain and T cell receptor (TCR)αβ.
  • In vitro assessment of T cell-dependent cytotoxicity against HER2-low cancer cell lines.
  • In vivo evaluation of TPP-45142 efficacy in HER2-low breast cancer xenograft models.
  • Assessment of TPP-45142 selectivity for tumor cells versus normal cardiac cells and cytokine release assay.

Main Results:

  • TPP-45142 demonstrated potent T cell-dependent killing of HER2-low cancer cells in vitro.
  • In vivo studies showed TPP-45142 inhibited tumor growth in HER2-low breast cancer xenografts.
  • TPP-45142 exhibited high selectivity for HER2-low tumor cells over normal cardiac cells, with a favorable therapeutic index.

Conclusions:

  • TPP-45142 is a promising next-generation TCE targeting HER2-low cancers.
  • The molecule recognizes a distinct HER2 epitope, offering a new therapeutic avenue.
  • TPP-45142 presents an improved safety profile, addressing unmet needs in HER2-targeted therapy.

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