Evidence map›Paper›PMID 41293918›Full record

ArticleXenotransplantation

Removal of Porcine Endogenous Retroviruses in Decellularized Liver Bioscaffolds.

Elena V A van Hengel, Dubravka Drabek, Henk P Roest, Jorke Willemse, Lieve J Reniers, Hera Stallmann, Jeroen de Jonge, Frank G Grosveld, Luc J W van der Laan, Monique M A Verstegen

Abstract read
In one paragraph

Article in Xenotransplantation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Elena V A van HengelDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Dubravka DrabekDepartment of Cell Biology, Erasmus MC, Rotterdam, the Netherlands.
Henk P RoestDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Jorke WillemseDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Lieve J ReniersDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Hera StallmannDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Jeroen de JongeDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Frank G GrosveldDepartment of Cell Biology, Erasmus MC, Rotterdam, the Netherlands.
Luc J W van der LaanDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.
Monique M A VerstegenDepartment of Surgery, Erasmus MC Transplant Institute, Rotterdam, the Netherlands.

Funding

the TKI-LSH (Topconsortium Kennis en Innovatie Life Sciences & Health) RELOADEMC-LSH19002
6 · The paper itself

Abstract

Tissue engineering using decellularized liver scaffolds presents a promising approach in regenerative medicine, offering a potential alternative to donor organ transplantation. The use of human livers as a bioscaffold is restricted by their limited availability and quality. Porcine livers offer an alternative due to their anatomical and physiological similarities to human livers. However, applying porcine-derived biomaterials in a clinical setting poses a risk of pathogen transmission, which is a noteworthy concern. Porcine endogenous retroviruses (PERVs), which are integrated into the genome of all pig breeds, are of particular concern, as subclasses PERV-A and PERV-B have shown to infect human cells in vitro. It is therefore essential to effectively remove all PERVs when manufacturing porcine scaffolds. In this study, we assessed the presence of PERV-specific DNA, RNA, and protein in decellularized porcine livers. Our findings prove that genetic and protein PERV material was effectively removed from porcine livers during our decellularization procedure. This finding substantiates the potential of using decellularized scaffolds of porcine origin for clinical applications without risk of PERV transmission.

Indexed as

Endogenous RetrovirusesLiverTissue EngineeringTissue ScaffoldsAnimalsHumansSwineTransplantation, Heterologousdecellularizationextracellular matrixliver bioengineeringporcine endogenous retrovirusesregenerative medicinetissue engineering

Identifiers

PMID41293918
PMCPMC12679514

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.