TY - JOUR
T1 - Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation
AU - Bender, Martin
AU - Abicht, Jan Michael
AU - Reichart, Bruno
AU - Neumann, Elisabeth
AU - Radan, Julia
AU - Mokelke, Maren
AU - Buttgereit, Ines
AU - Leuschen, Maria
AU - Wall, Felicia
AU - Michel, Sebastian
AU - Ellgass, Reinhard
AU - Steen, Stig
AU - Paskevicius, Audrius
AU - Lange, Andreas
AU - Kessler, Barbara
AU - Kemter, Elisabeth
AU - Klymiuk, Nikolai
AU - Denner, Joachim
AU - Godehardt, Antonia W.
AU - Tönjes, Ralf R.
AU - Burgmann, Jonathan M.
AU - Figueiredo, Constança
AU - Milusev, Anastasia
AU - Zollet, Valentina
AU - Salimi-Afjani, Neda
AU - Despont, Alain
AU - Rieben, Robert
AU - Ledderose, Stephan
AU - Walz, Christoph
AU - Hagl, Christian
AU - Ayares, David
AU - Wolf, Eckhard
AU - Schmoeckel, Michael
AU - Brenner, Paolo
AU - Binder, Uli
AU - Gebauer, Michaela
AU - Skerra, Arne
AU - Längin, Matthias
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/8
Y1 - 2024/8
N2 - 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.
AB - 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.
KW - CD40/CD40L
KW - co-stimulation blockade
KW - heart
KW - orthotopic heart transplantation
KW - xenotransplantation
UR - http://www.scopus.com/inward/record.url?scp=85202628385&partnerID=8YFLogxK
U2 - 10.3390/biomedicines12081927
DO - 10.3390/biomedicines12081927
M3 - Article
AN - SCOPUS:85202628385
SN - 2227-9059
VL - 12
JO - Biomedicines
JF - Biomedicines
IS - 8
M1 - 1927
ER -