Preformed donor-specific antibodies are associated with acute rejection and biliary complications after liver transplantation: A Swiss Transplant Cohort Study analysis
The impact of preformed donor-specific antibodies (DSA) in liver transplantation (LT) remains controversial despite evidence linking their presence to an increased risk of early allograft damage, as well as antibody- and T cell-mediated rejection. In this nationwide analysis, preformed DSA were assessed using single antigen bead assays [positive if mean fluorescence intensity (MFI) ≥1000]. This study included all LT recipients enrolled in the Swiss Transplant Cohort Study (STCS) who underwent LT between 2014 and 2016. One-year post-LT outcomes including cumulative allograft and patient survival, as well as the incidence of biliary, vascular, and infectious complications were compared between DSA-positive (DSA+) and -negative (DSA-) individuals. Among 321 LT performed in 306 patients, preformed DSA were detected in 92 (28.7%) and more frequently observed in patients with a history of prior transplantation (p=0.008) or autoimmune liver disease (p=0.036). Class I and II DSA were present in 48.9% and 71.1% of DSA+ cases, with concomitant class I and II DSA in 20.7%. The median (IQR) cumulative MFI (cMFI) of the preformed DSA was 3768 (1875-10537) and 52.2% of DSA+ patients harbored multiple DSA. While overall patient survival did not differ between DSA+ and DSA- individuals, DSA+ patients with cMFI ≥5000 exhibited a higher incidence of allograft failure and biopsy-proven rejection. Multivariate analysis revealed that the presence of preformed DSA was independently associated with biliary complications (HR 2.26, 95% CI 1.17-4.37, p=0.02) but not with vascular or infectious complications. In summary, preformed DSA were associated with biliary complications, increased rejection, and reduced allograft survival. These findings suggest pre-transplant immunological risk assessment and the need for tailored immunosuppressive strategies in LT.
Authors
- Yannick D. Müller (ORCID: https://orcid.org/0000-0003-0513-7156)
- Giuseppe Pantaleo (ORCID: https://orcid.org/0000-0003-3651-2721)
- Linard Hoessly (ORCID: https://orcid.org/0000-0002-2745-2141)
- V. McLin
- Nicolas J. Mueller (ORCID: https://orcid.org/0000-0002-1059-3191)
- Rafaela da Silva (ORCID: https://orcid.org/0000-0002-3335-2542)
- Loreta Kavaliukaite
- S Schaub
- Urs Wirthmüller
- José Oberholzer (ORCID: https://orcid.org/0000-0002-1069-2501)
- Nathalie Rock (ORCID: https://orcid.org/0000-0001-5315-9267)
- Jean Villard
- Vanessa Banz (ORCID: https://orcid.org/0000-0002-4887-5776)
- Jakob Nilsson (ORCID: https://orcid.org/0000-0001-5091-8133)
- Susanne Stampf (ORCID: https://orcid.org/0000-0003-3399-5078)
- Darius Moradpour (ORCID: https://orcid.org/0000-0003-1977-6792)
- A. Berzigotti
- Matthias Niemann (ORCID: https://orcid.org/0000-0002-3514-9812)
- Nicolas Goossens (ORCID: https://orcid.org/0000-0002-8698-4690)
- David Semela (ORCID: https://orcid.org/0000-0002-7201-743X)
- Barbara E. Wildhaber (ORCID: https://orcid.org/0000-0003-4548-382X)
- Sylvie Ferrari-Lacraz
- Oriol Josep Manuel
- Montserrat Fraga
- Julien Vionnet
- Giulia Magini
- Christine Bernsmeier
- Philipp Dutkowski
- Pascale Tinguely
- Dela Golshayan
- Philippe Compagnon
- Manuel Pascual
- Andreas E. Kremer
- Myriam Amrari
- the Swiss Transplant Cohort Studyx (STCS)
- Antonio Mancarella
- Michael Koller
Institutions
- University of Geneva (CH)
- University of Bern (CH)
- Kantonsspital St. Gallen (CH)
- University Hospital of Bern (CH)
- University Hospital of Basel (CH)
- Roche Pharma AG (Germany) (DE)
- University Hospital of Zurich (CH)
- ENT and Allergy (US)
- University Hospital of Geneva (CH)
- Civil Service (GB)
- Swiss HIV Cohort Study (CH)
- Artistic Realization Technologies (US)
- Geneva College (US)
- University of Lausanne (CH)
Publication Details
- Journal
- Liver Transplantation
- Published
- 2026-03-26
- DOI
- https://doi.org/10.1097/lvt.0000000000000861
- Primary Topic
- Organ Transplantation Techniques and Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00