Evidence map›Paper›PMID 29604134›Full record

ReviewXenotransplantation2018

B4GALNT2 and xenotransplantation: A newly appreciated xenogeneic antigen.

Guerard Byrne, Saadullah Ahmad-Villiers, Zeji Du, Christopher McGregor

Open access · hybridAbstract readReview
In one paragraph

Review in Xenotransplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
12.1field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 126 citations in OpenAlex.

  1. Article
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  8. Review
  9. Effect of Dead-CellAnimals : an open access journal from MDPI · 2025
    Article
  10. Immunometabolism of Liver Xenotransplantation and Prospective Solutions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  11. Review
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  13. Review
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  15. Review
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  17. Article
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8 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Guerard ByrneInstitute of Cardiovascular Science, University College London, London, UK.ORCID 0000-0003-1897-1289
Saadullah Ahmad-VilliersInstitute of Cardiovascular Science, University College London, London, UK.
Zeji DuDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Christopher McGregorInstitute of Cardiovascular Science, University College London, London, UK.
Mayo Clinic · USUniversity College London · GB

Funding

Studies in pig-to-primate cardiac xenotransplantationU01AI066310 · NIAID · MAYO CLINIC ROCHESTER · PI MCGREGOR, CHRISTOPHER G.A. · 2005 to 2014
$9.5M
MRC MR/R006393NIAID NIH HHS U01 AI066310NIH HHS AI066310NIHR UCL Biomedical Research Centre
6 · The paper itself

Abstract

Analysis of non-Gal antibody induced after pig-to-baboon cardiac xenotransplantation identified the glycan produced by porcine beta-1,4-N-acetyl-galactosaminyltransferase 2 (B4GALNT2) as an immunogenic xenotransplantation antigen. The porcine B4GALNT2 enzyme is homologous to the human enzyme, which synthesizes the human SDa blood group antigen. Most humans produce low levels of anti-SDa IgM which polyagglutinates red blood cells from rare individuals with high levels of SDa expression. The SDa glycan is also present on GM2 gangliosides. Clinical GM2 vaccination studies for melanoma patients suggest that a human antibody response to SDa can be induced. Expression of porcine B4GALNT2 in human HEK293 cells results in increased binding of anti-SDa antibody and increased binding of Dolichos biflorus agglutinin (DBA), a lectin commonly used to detect SDa. In pigs, B4GALNT2 is expressed by vascular endothelial cells and endothelial cells from a wide variety of pig backgrounds stain with DBA, suggesting that porcine vascular expression of B4GALNT2 is not polymorphic. Mutations in B4GALNT2 have been engineered in mice and pigs. In both species, the B4GALNT2-KO animals are apparently normal and no longer show evidence of SDa antigen expression. Pig tissues with a mutation in B4GALNT2, added to a background of alpha-1,3-galactosyltransferase deficient (GGTA1-KO) and cytidine monophosphate-N-acetylneuraminic acid hydroxylase deficient (CMAH-KO), show reduced antibody binding, confirming the presence of B4GALNT2-dependent antibodies in both humans and non-human primates. Preclinical xenotransplantation using B4GALNT2-deficient donors has recently been reported. Elimination of this source of immunogenic pig antigen should minimize acute injury by preformed anti-pig antibody and eliminate an induced clinical immune response to this newly appreciated xenotransplantation antigen.

Indexed as

Transplantation, HeterologousAnimalsAnimals, Genetically ModifiedGalactosyltransferasesGene Knockout TechniquesGraft RejectionHeterograftsHumansGalactosyltransferasesN-acetyllactosaminide alpha-1,3-galactosyltransferaseantibody-mediated rejectionbeta-1,4-N-acetyl-galactosaminyltransferase 2cardiac xenotransplantationgenetic modificationxenotransplantation

Identifiers

PMID29604134
PMCPMC6158069
OpenAlexW2795021051

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.