Evidence map›Paper›PMID 24554032›Full record

ArticleArchivum immunologiae et therapiae experimentalis2014

Double transgenic pigs with combined expression of human α1,2-fucosyltransferase and α-galactosidase designed to avoid hyperacute xenograft rejection.

Joanna Zeyland, Anna Woźniak, Barbara Gawrońska, Wojciech Juzwa, Jacek Jura, Agnieszka Nowak, Ryszard Słomski, Zdzisław Smorąg, Marlena Szalata, Urszula Mazurek and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Archivum immunologiae et therapiae experimentalis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Immunometabolism of Liver Xenotransplantation and Prospective Solutions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Biomaterials in Valvular Heart Diseases.Frontiers in bioengineering and biotechnology · 2020
    Review
  12. Review
  13. Article
  14. Immune modulation in xenotransplantation.Archivum immunologiae et therapiae experimentalis · 2015
    Review
  15. Article
  16. The current state of xenotransplantation.Journal of applied genetics · 2015
    Review
  17. Article
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

11 authors at 5 institutions in 1 country.

Joanna ZeylandDepartment of Biochemistry and Biotechnology, Poznan University of Life Sciences, Dojazd 11, 60-632, Poznan, Poland, jzeyland@yahoo.com.
Anna Woźniak
Barbara Gawrońska
Wojciech Juzwa
Jacek Jura
Agnieszka Nowak
Ryszard Słomski
Zdzisław Smorąg
Marlena Szalata
Urszula Mazurek
Daniel Lipiński
University of Life Sciences in Poznań · PLNational Research Institute of Animal Production · PLPolish Academy of Sciences · PLInstitute of Human Genetics · PLMedical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperacute rejection (HAR) depends on the response of xenoreactive antibodies principally against porcine α-Gal epitope. Methods eliminating HAR include GGTA1 inactivation, regulation of the complement system and modification of the oligosaccharide structure of surface proteins in donor's cells. Transgenic animals designed for the purpose of xenotransplantation with single modification do not display full reduction of the α-Gal epitope level, which means that a accumulation of several modifications in one transgenic individual is needed. The aim of the study was to create a molecular and cytogenetic profile of a double transgenic animal with α1,2-fucosyltransferase and α-galactosidase expression. As a result of interbreeding of an individual with α1,2-fucosyltransferase expression with an individual with α-galactosidase expression 12 living piglets were obtained. PCR revealed the pCMVFUT gene construct was present in four individuals and pGAL-GFPBsd in three, including one with a confirmed integration of both the gene constructs. Fluorescence in situ hybridization confirmed the site of transgene integration, which corresponded to the mapping site of the transgenes which occurred in the parental generations. Karyotype analysis did not show any changes in the structure or the number of chromosomes (2n = 38, XX). As for the results pertaining to the single transgenic individuals, expression analysis demonstrated a high extent of α-Gal epitope level reduction on the surface of cells, whereas human serum cytotoxicity tests revealed the smallest decrease in longevity of cells in the obtained double transgenic individual (4.35 %). The tests suggest that the co-expression of both the transgenes leads to a considerable reduction of the α-Gal antigen level on the surface of cells and a decrease of xenotransplant immunogenicity.

Indexed as

Transplantation, Heterologousalpha-GalactosidaseAnimalsAnimals, Genetically ModifiedAntibody-Dependent Cell CytotoxicityCell LineEpitopes, B-LymphocyteFibroblastsFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferaseGraft RejectionHumansImmunity, HumoralSerumSwinealpha-GalactosidaseEpitopes, B-LymphocyteFucosyltransferasesGalactoside 2-alpha-L-fucosyltransferase

Identifiers

PMID24554032
PMCPMC4164832
OpenAlexW1971574556

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Registered trials

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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.