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T-Cell Engager Antibodies Enable T Cells to Control Hbv Infection and to Target Hbsag-Positive Hepatoma in Mice Publisher Pubmed



Quitt O1 ; Luo S1 ; Meyer M2 ; Xie Z1 ; Golsazshirazi F3 ; Loffredoverde E1 ; Festag J1 ; Bockmann JH1, 5, 6 ; Zhao L1 ; Stadler D1 ; Chou WM1 ; Tedjokusumo R1 ; Wettengel JM1 ; Ko C1 Show All Authors
Authors
  1. Quitt O1
  2. Luo S1
  3. Meyer M2
  4. Xie Z1
  5. Golsazshirazi F3
  6. Loffredoverde E1
  7. Festag J1
  8. Bockmann JH1, 5, 6
  9. Zhao L1
  10. Stadler D1
  11. Chou WM1
  12. Tedjokusumo R1
  13. Wettengel JM1
  14. Ko C1
  15. Noener E1
  16. Bulbuc N2
  17. Shokri F3
  18. Luttgau S4
  19. Heikenwalder M1
  20. Bohne F1
  21. Moldenhauer G4
  22. Momburg F2
  23. Protzer U1, 5
Show Affiliations
Authors Affiliations
  1. 1. Institute of Virology, School of Medicine, Technical University of Munich, Helmholtz Zentrum Munchen, Munich, Germany
  2. 2. Antigen Presentation and T/NK Cell Activation Group, Clinical Cooperation Unit Applied Tumor Immunity, German Cancer Research Centre, Heidelberg, Germany
  3. 3. Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Translational Immunology, German Cancer Research Centre, Heidelberg, Germany
  5. 5. German Center for Infection Research (DZIF), Munich and Hamburg Partner sites, Germany
  6. 6. Department of Internal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

Source: Journal of Hepatology Published:2021


Abstract

Background & Aims: Current antiviral therapies control but rarely eliminate HBV, leaving chronic HBV carriers at risk of developing hepatocellular carcinoma (HCC). Lacking or dysfunctional virus-specific adaptive immunity prevents control of HBV and allows the virus to persist. Restoring antiviral T-cell immunity could lead to HBV elimination and cure of chronically infected patients. Methods: We constructed bispecific T-cell engager antibodies that are designed to induce antiviral immunity through simultaneous binding of HBV envelope proteins (HBVenv) on infected hepatocytes and CD3 or CD28 on T cells. T-cell engager antibodies were employed in co-cultures with healthy donor lymphocytes and HBV-infected target cells. Activation of the T-cell response was determined by detection of pro-inflammatory cytokines, effector function (by cytotoxicity) and antiviral effects. To study in vivo efficacy, immune-deficient mice were transplanted with HBVenv-positive and -negative hepatoma cells. Results: The 2 T-cell engager antibodies synergistically activated T cells to become polyfunctional effectors that in turn elicited potent antiviral effects by killing infected cells and in addition controlled HBV via non-cytolytic, cytokine-mediated antiviral mechanisms. In vivo in mice, the antibodies attracted T cells specifically to the tumors expressing HBVenv resulting in T-cell activation, tumor infiltration and reduction of tumor burden. Conclusion: This study demonstrates that the administration of HBVenv-targeting T-cell engager antibodies facilitates a robust T-cell redirection towards HBV-positive target cells and provides a feasible and promising approach for the treatment of chronic viral hepatitis and HBV-associated HCC. Lay summary: T-cell engager antibodies are an interesting, novel therapeutic tool to restore immunity in patients with chronic hepatitis B. As bispecific antibodies, they bind envelope proteins on the surface of the hepatitis B virus (HBV) and CD3 or CD28 on T cells. This way, they induce a potent antiviral and cytotoxic T-cell response that leads to the elimination of HBV-positive cells. These bispecific T-cell engager antibodies are exciting therapeutic candidates for chronic hepatitis B and HBV-associated hepatocellular carcinoma. © 2021 European Association for the Study of the Liver