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

cris.virtual.author-orcid0000-0003-4179-8891
cris.virtualsource.author-orcid3bee1d6a-134c-4ed9-a1b8-a49005692c8e
cris.virtualsource.author-orcid61ce3036-6e14-4565-8138-b7094d8cfef2
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cris.virtualsource.author-orcid6eb58dfd-9fde-4638-ad45-a6946d31d2e0
datacite.rightsopen.access
dc.contributor.authorBender, Martin
dc.contributor.authorAbicht, Jan-Michael
dc.contributor.authorReichart, Bruno
dc.contributor.authorNeumann, Elisabeth
dc.contributor.authorRadan, Julia
dc.contributor.authorMokelke, Maren
dc.contributor.authorButtgereit, Ines
dc.contributor.authorLeuschen, Maria
dc.contributor.authorWall, Felicia
dc.contributor.authorMichel, Sebastian
dc.contributor.authorEllgass, Reinhard
dc.contributor.authorSteen, Stig
dc.contributor.authorPaskevicius, Audrius
dc.contributor.authorLange, Andreas
dc.contributor.authorKessler, Barbara
dc.contributor.authorKemter, Elisabeth
dc.contributor.authorKlymiuk, Nikolai
dc.contributor.authorDenner, Joachim
dc.contributor.authorGodehardt, Antonia W
dc.contributor.authorTönjes, Ralf R
dc.contributor.authorBurgmann, Jonathan M
dc.contributor.authorFigueiredo, Constança
dc.contributor.authorMilusev, Anastasia
dc.contributor.authorZollet, Valentina
dc.contributor.authorSalimi Afjani, Neda
dc.contributor.authorDespont, Alain
dc.contributor.authorRieben, Robert
dc.contributor.authorLedderose, Stephan
dc.contributor.authorWalz, Christoph
dc.contributor.authorHagl, Christian
dc.contributor.authorAyares, David
dc.contributor.authorWolf, Eckhard
dc.contributor.authorSchmoeckel, Michael
dc.contributor.authorBrenner, Paolo
dc.contributor.authorBinder, Uli
dc.contributor.authorGebauer, Michaela
dc.contributor.authorSkerra, Arne
dc.contributor.authorLängin, Matthias
dc.date.accessioned2024-10-08T12:53:12Z
dc.date.available2024-10-08T12:53:12Z
dc.date.issued2024-08-22
dc.description.abstractThe 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.
dc.description.numberOfPages21
dc.description.sponsorshipGraduate School for Cellular and Biomedical Sciences (GCB)
dc.description.sponsorshipDepartment for BioMedical Research, Forschungsgruppe Herz und Gefässe
dc.description.sponsorshipDepartment for BioMedical Research (DBMR)
dc.description.sponsorshipDepartment for BioMedical Research, Gruppe Rieben
dc.identifier.doi10.48620/8424
dc.identifier.pmid39200391
dc.identifier.publisherDOI10.3390/biomedicines12081927
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/44735
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofBiomedicines
dc.relation.issn2227-9059
dc.subjectCD40/CD40L
dc.subjectco-stimulation blockade
dc.subjectheart
dc.subjectorthotopic heart transplantation
dc.subjectxenotransplantation
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleCombination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue8
oaire.citation.volume12
oairecerif.author.affiliationDepartment for BioMedical Research, Gruppe Rieben
oairecerif.author.affiliationDepartment for BioMedical Research, Gruppe Rieben
oairecerif.author.affiliationDepartment for BioMedical Research, Gruppe Rieben
oairecerif.author.affiliationDepartment for BioMedical Research, Forschungsgruppe Herz und Gefässe
oairecerif.author.affiliationDepartment for BioMedical Research (DBMR)
oairecerif.author.affiliation2Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
oairecerif.author.affiliation2Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
oairecerif.author.affiliation2Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
oairecerif.author.affiliation2Department for BioMedical Research (DBMR)
oairecerif.author.affiliation2Department for BioMedical Research, Gruppe Rieben
oairecerif.author.affiliation3Department for BioMedical Research, Gruppe Rieben
oairecerif.author.affiliation3Department for BioMedical Research, Forschungsgruppe Herz und Gefässe
unibe.additional.sponsorshipGraduate School for Cellular and Biomedical Sciences (GCB)
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unibe.subtype.articlejournal

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