Biomedicines (Aug 2024)
Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation
- Martin Bender,
- Jan-Michael Abicht,
- Bruno Reichart,
- Elisabeth Neumann,
- Julia Radan,
- Maren Mokelke,
- Ines Buttgereit,
- Maria Leuschen,
- Felicia Wall,
- Sebastian Michel,
- Reinhard Ellgass,
- Stig Steen,
- Audrius Paskevicius,
- Andreas Lange,
- Barbara Kessler,
- Elisabeth Kemter,
- Nikolai Klymiuk,
- Joachim Denner,
- Antonia W. Godehardt,
- Ralf R. Tönjes,
- Jonathan M. Burgmann,
- Constança Figueiredo,
- Anastasia Milusev,
- Valentina Zollet,
- Neda Salimi-Afjani,
- Alain Despont,
- Robert Rieben,
- Stephan Ledderose,
- Christoph Walz,
- Christian Hagl,
- David Ayares,
- Eckhard Wolf,
- Michael Schmoeckel,
- Paolo Brenner,
- Uli Binder,
- Michaela Gebauer,
- Arne Skerra,
- Matthias Längin
Affiliations
- Martin Bender
- Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany
- Jan-Michael Abicht
- Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany
- Bruno Reichart
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Elisabeth Neumann
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Julia Radan
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Maren Mokelke
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Ines Buttgereit
- Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany
- Maria Leuschen
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Felicia Wall
- Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany
- Sebastian Michel
- Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany
- Reinhard Ellgass
- Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany
- Stig Steen
- Department of Cardiothoracic Surgery, Lund University and Skåne University Hospital, 22242 Lund, Sweden
- Audrius Paskevicius
- Department of Cardiothoracic Surgery, Lund University and Skåne University Hospital, 22242 Lund, Sweden
- Andreas Lange
- Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany
- Barbara Kessler
- Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany
- Elisabeth Kemter
- Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany
- Nikolai Klymiuk
- Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany
- Joachim Denner
- Institute of Virology, Free University Berlin, 14163 Berlin, Germany
- Antonia W. Godehardt
- Division of Haematology, Cell and Gene Therapy, Paul-Ehrlich-Institut, 63225 Langen, Germany
- Ralf R. Tönjes
- Division of Haematology, Cell and Gene Therapy, Paul-Ehrlich-Institut, 63225 Langen, Germany
- Jonathan M. Burgmann
- Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, 30625 Hannover, Germany
- Constança Figueiredo
- Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, 30625 Hannover, Germany
- Anastasia Milusev
- Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland
- Valentina Zollet
- Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland
- Neda Salimi-Afjani
- Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland
- Alain Despont
- Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland
- Robert Rieben
- Department for BioMedical Research (DBMR), University of Bern, 3008 Bern, Switzerland
- Stephan Ledderose
- Institute of Pathology, Faculty of Medicine, LMU Munich, 81377 Munich, Germany
- Christoph Walz
- Institute of Pathology, Faculty of Medicine, LMU Munich, 81377 Munich, Germany
- Christian Hagl
- Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany
- David Ayares
- Revivicor, Blacksburg, VA 24060, USA
- Eckhard Wolf
- Institute of Molecular Animal Breeding and Biotechnology, Gene Center, and Department of Veterinary Sciences, LMU Munich, 81377 Munich, Germany
- Michael Schmoeckel
- Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany
- Paolo Brenner
- Department of Cardiac Surgery, University Hospital, LMU Munich, 81377 Munich, Germany
- Uli Binder
- XL-protein GmbH, 85354 Freising, Germany
- Michaela Gebauer
- XL-protein GmbH, 85354 Freising, Germany
- Arne Skerra
- Chair of Biological Chemistry, School of Life Sciences, Technical University of Munich, 85354 Freising, Germany
- Matthias Längin
- Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany
- DOI
- https://doi.org/10.3390/biomedicines12081927
- Journal volume & issue
-
Vol. 12,
no. 8
p. 1927
Abstract
The blockade of the CD40/CD40L immune checkpoint is considered essential for cardiac xenotransplantation. However, it is still unclear which single antibody directed against CD40 or CD40L (CD154), or which combination of antibodies, is better at preventing organ rejection. For example, the high doses of antibody administered in previous experiments might not be feasible for the treatment of humans, while thrombotic side effects were described for first-generation anti-CD40L antibodies. To address these issues, we conducted six orthotopic pig-to-baboon cardiac xenotransplantation experiments, combining a chimeric anti-CD40 antibody with an investigational long-acting PASylated anti-CD40L Fab fragment. The combination therapy effectively resulted in animal survival with a rate comparable to a previous study that utilized anti-CD40 monotherapy. Importantly, no incidence of thromboembolic events associated with the administration of the anti-CD40L PAS-Fab was observed. Two experiments failed early because of technical reasons, two were terminated deliberately after 90 days with the baboons in excellent condition and two were extended to 120 and 170 days, respectively. Unexpectedly, and despite the absence of any clinical signs, histopathology revealed fungal infections in all four recipients. This study provides, for the first time, insights into a combination therapy with anti-CD40/anti-CD40L antibodies to block this immune checkpoint.
Keywords