Evidence map›Paper›PMID 40757507›Full record

ArticleGlycobiology2025

Glycoengineering of nematode antigens using insect cells: a promising approach for producing bioactive vaccine antigens of the barber's pole worm Haemonchus contortus.

Isabella Adduci, Floriana Sajovitz-Grohmann, Licha N Wortha, Zuzanna Dutkiewicz, Hugo Weidinger, Anja Joachim, Thomas Wittek, Dirk Werling, Iain B H Wilson, Katharina Lichtmannsperger and 1 more

Abstract read
In one paragraph

Article in Glycobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Deciphering theBiomolecules · 2025
    Review
  2. 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.

Isabella AdduciDepartment of Biological Sciences and Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Floriana Sajovitz-GrohmannClinical Centre for Ruminant and Camelid Medicine, Clinical Department for Farm Animals and Food System Science, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Licha N WorthaDepartment of Biological Sciences and Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Zuzanna DutkiewiczFaculty of Biology, Department of Microbiology, University of Innsbruck, Innsbruck 6020, Austria.ORCID 0000-0003-0444-5931
Hugo WeidingerDepartment of Biological Sciences and Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Anja JoachimDepartment of Biological Sciences and Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Thomas WittekClinical Centre for Ruminant and Camelid Medicine, Clinical Department for Farm Animals and Food System Science, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Dirk WerlingDepartment of Pathobiology and Population Sciences, Centre for Vaccinology and Regenerative Medicine, Royal Veterinary College, Hatfield, AL9 7TA, United Kingdom.
Iain B H WilsonInstitute of Biochemistry, University of Natural Resources and Life Sciences, Vienna, Muthgasse 18, Vienna 1190, Austria.ORCID 0000-0001-8996-1518
Katharina LichtmannspergerClinical Centre for Ruminant and Camelid Medicine, Clinical Department for Farm Animals and Food System Science, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.
Shi YanDepartment of Biological Sciences and Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Veterinärplatz 1, Vienna 1210, Austria.ORCID 0000-0003-4949-9140

Funding

Vetmeduni Vienna
6 · The paper itself

Abstract

The H11 antigens, located on the intestinal microvilli of Haemonchus contortus, comprise a group of homologous aminopeptidases essential for the parasite's digestion of blood meals. Native H11 proteins are promising vaccine antigens, capable of eliciting robust protective immunity against H. contortus in sheep and goats. However, recombinant forms of H11, produced either in conventional expression systems or in transgenic Caenorhabditis elegans, failed to replicate the protective efficacy of the native form, most likely due to two critical factors: improper glycosylation and protein misfolding. To address these limitations, we developed a novel strategy to produce recombinant Haemonchus antigens in glycoengineered insect cells. By introducing three C. elegans genes that alter the native N-glycosylation pathways of Hi5 insect cells we successfully expressed soluble H11 and GA1 antigens featuring nematode-specific glycan epitopes, including tri-fucosylated structures and the Galβ1,4Fuc motif. The glycoengineered H11 proteins retained aminopeptidase activity and stimulated cytokine secretion from ovine peripheral blood mononuclear cells in vitro. These findings establish a platform for producing bioactive vaccine antigens against the parasitic nematode H. contortus.

Indexed as

Antigens, HelminthHaemonchusHelminth ProteinsVaccinesAnimalsCaenorhabditis elegansGlycosylationHaemonchiasisInsectaSheepAntigens, HelminthHelminth ProteinsVaccinesglycoengineeringglycoproteininsect cellparasite antigenvaccine

Identifiers

PMID40757507
PMCPMC12343074

What OpenQuestion holds

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LicenceCC BY-NC
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.