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813 Combination of HexaBody-CD27 with PD-(L)1 blockade potentiates single-agent activity leading to enhanced human T-cell effector functions in vitro
  1. Andrea Imle1,
  2. Isil Altintas2,
  3. Kristina Nuermberger1,
  4. Jordan Blum3,
  5. Anna-Lena Krause1,
  6. Aras Toker1,
  7. Lidia Daszkiewicz2,
  8. Alexander Muik1,
  9. Friederike Gieseke1,
  10. Tahamtan Ahmadi3,
  11. Sina Fellermeier-Kopf1,
  12. Kristel Kemper2,
  13. Oezlem Tuereci1,
  14. Esther Breij2 and
  15. Ugur Sahin1
  1. 1BioNTech SE, Mainz, Germany
  2. 2Genmab, Utrecht, Netherlands
  3. 3Genmab, Plainsboro, NJ, USA
  • Journal for ImmunoTherapy of Cancer (JITC) preprint. The copyright holder for this preprint are the authors/funders, who have granted JITC permission to display the preprint. All rights reserved. No reuse allowed without permission.


Background Activation of the T-cell co-stimulatory receptor CD27 and blockade of the PD-1:PD-L1 axis can augment antitumor immune responses through distinct mechanisms. HexaBody®-CD27 (GEN1053/BNT313) is a novel CD27 human monoclonal antibody with a functionally inert IgG1 Fc domain harboring a hexamerization-enhancing mutation to induce CD27 activation independently of Fc gamma receptor crosslinking, while also avoiding T-cell depletion. This unique mechanism of action distinguishes HexaBody-CD27 from other CD27-targeting monoclonal antibodies. In preclinical studies, HexaBody-CD27 enhanced proliferation and effector functions of activated T cells.

Methods The effects of combining HexaBody-CD27 with anti-PD-(L)1 antibodies (pembrolizumab, nivolumab, and atezolizumab) on human CD8+ T-cell proliferation and effector functions were investigated in vitro. CD8+ T-cell proliferation and cytokine secretion were assessed in an antigen-specific assay using claudin-6 as a model antigen. Cytotoxic activity of claudin-6-specific human CD8+ T cells towards MDA-MB-231 tumor cells expressing cognate antigen was analyzed using real-time analysis of tumor cell mass, along with flow cytometric analysis of granzyme B and CD107a expression on CD8+ T cells. The effect of combining HexaBody-CD27 with pembrolizumab on IFN-γ secretion was evaluated in a mixed lymphocyte reaction (MLR) assay, with synergy analysis using the Highest Single Agent model.

Results Combination treatment with HexaBody-CD27 and all tested anti-PD-(L)1 antibodies enhanced proliferation and proinflammatory cytokine secretion of antigen-specific CD8+ T cells in coculture with cognate antigen-expressing dendritic cells, compared to the respective single-agent treatments. Furthermore, the combination increased granzyme B and CD107a expression by antigen-specific CD8+ T-cells and enhanced CD8+ T-cell-mediated cytotoxic activity towards cognate antigen-expressing tumor cells. In MLR assays of human CD8+ T cells and allogeneic dendritic cells, the combination of HexaBody-CD27 and pembrolizumab synergistically enhanced IFN-γ secretion.

Conclusions The combination of HexaBody-CD27 with anti-PD-(L)1 antibodies potentiates the effects of each single agent on effector functions of antigen-specific T cells in vitro. This study provides preclinical rationale for investigation of this combination in clinical trials. HexaBody-CD27 is currently being evaluated in patients with advanced solid tumors (NCT05435339).

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