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  3. Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation.
 

Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation.

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BORIS DOI
10.48620/8424
Publisher DOI
10.3390/biomedicines12081927
PubMed ID
39200391
Description
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.
Date of Publication
2024-08-22
Publication Type
Article
Subject(s)
600 - Technology::610 - Medicine & health
Keyword(s)
CD40/CD40L
•
co-stimulation blockade
•
heart
•
orthotopic heart transplantation
•
xenotransplantation
Language(s)
en
Contributor(s)
Bender, Martin
Abicht, Jan-Michael
Reichart, Bruno
Neumann, Elisabeth
Radan, Julia
Mokelke, Maren
Buttgereit, Ines
Leuschen, Maria
Wall, Felicia
Michel, Sebastian
Ellgass, Reinhard
Steen, Stig
Paskevicius, Audrius
Lange, Andreas
Kessler, Barbara
Kemter, Elisabeth
Klymiuk, Nikolai
Denner, Joachim
Godehardt, Antonia W
Tönjes, Ralf R
Burgmann, Jonathan M
Figueiredo, Constança
Milusev, Anastasia
Department for BioMedical Research, Gruppe Rieben
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Zollet, Valentina
Department for BioMedical Research, Gruppe Rieben
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Salimi Afjani, Nedaorcid-logo
Department for BioMedical Research, Gruppe Rieben
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Despont, Alain
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Department for BioMedical Research (DBMR)
Department for BioMedical Research, Gruppe Rieben
Rieben, Robertorcid-logo
Department for BioMedical Research (DBMR)
Department for BioMedical Research, Gruppe Rieben
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Ledderose, Stephan
Walz, Christoph
Hagl, Christian
Ayares, David
Wolf, Eckhard
Schmoeckel, Michael
Brenner, Paolo
Binder, Uli
Gebauer, Michaela
Skerra, Arne
Längin, Matthias
Additional Credits
Graduate School for Cellular and Biomedical Sciences (GCB)
Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
Department for BioMedical Research (DBMR)
Department for BioMedical Research, Gruppe Rieben
Series
Biomedicines
Publisher
MDPI
ISSN
2227-9059
Access(Rights)
open.access
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