Evidence map›Paper›PMID 42815557›Full record

ArticleParasite immunology2026

Vaccination With Trichuris muris Poly-Cysteine and Histidine-Tailed Protein p43 Protects Against Chronic Infection.

Allison J Bancroft, Kelly S Hayes, Laura Campbell, Seona Thompson, Christina Dold, Luke Blackwell, Christine S Rollier, David J Thornton, Richard K Grencis

Abstract read
In one paragraph

Article in Parasite immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Allison J BancroftLydia Becker Institute for Immunology and Inflammation, Manchester, UK.
Kelly S HayesLydia Becker Institute for Immunology and Inflammation, Manchester, UK.ORCID https://orcid.org/0000-0003-3034-048X
Laura CampbellLydia Becker Institute for Immunology and Inflammation, Manchester, UK.
Seona ThompsonLydia Becker Institute for Immunology and Inflammation, Manchester, UK.
Christina DoldDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford and the NIHR Oxford Biomedical Research Centre, CCVTM, Churchill Lane, Oxford, UK.
Luke BlackwellDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford and the NIHR Oxford Biomedical Research Centre, CCVTM, Churchill Lane, Oxford, UK.
Christine S RollierDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford and the NIHR Oxford Biomedical Research Centre, CCVTM, Churchill Lane, Oxford, UK.
David J ThorntonLydia Becker Institute for Immunology and Inflammation, Manchester, UK.ORCID https://orcid.org/0000-0001-7148-1970
Richard K GrencisLydia Becker Institute for Immunology and Inflammation, Manchester, UK.ORCID https://orcid.org/0000-0002-7592-0085

Funding

Wellcome TrustWellcome Trust 088785/Z/09/ZWellcome Trust Z10661/Z/18/Z
6 · The paper itself

Abstract

Trichuris trichiura is one of the soil transmitted geohelminths which together currently affect approximately 25% of the global population resulting in considerable morbidity particularly in children and young adults. Recent estimates put infection by T. trichiura at approximately 513 million. De-worming programmes are often not completely effective against T. trichiura and fail to provide resistance to reinfection. Vaccination against these multicellular parasites has proved difficult as they have complex antigenic make-up and the potential to harness the host immune system to their own advantage. Previous vaccination experiments in mice using excretory secretory (ES) material have proved successful although the specific antigens responsible for protection have remained elusive. Here we show that vaccination of mice with native (n)p43, the dominant secreted protein from adult T. muris, formulated with Alum adjuvant can protect against chronic infection. The vaccine candidate generated a strong Type 2 response and host protection was dependent on signalling through IL-4 Rα. Vaccination with a recombinant (r)p43 formulated with alum resulted in stunted worms and reduced worm fecundity but no significant reduction in worm burden. Deglycosylation of np43 significantly abrogated protection against infection suggesting p43 glycans play a role in mediating the protective efficacy of np43. Vaccination using an adenoviral p43 construct generated a robust antibody response to np43 but no protection against challenge infection. Orthologues of p43 are present in other closely related nematodes including T. trichiura and T. suis which infects wild and domestic pigs, suggesting potential for similar vaccine development for both human and veterinary trichiuriasis.

Indexed as

Antigens, HelminthHelminth ProteinsPersistent InfectionTrichuriasisTrichurisAdjuvants, ImmunologicAlum CompoundsAnimalsAntibodies, HelminthFemaleMiceProtein Subunit VaccinesVaccinationAdjuvants, ImmunologicAlum Compoundsaluminum sulfateAntibodies, HelminthAntigens, HelminthHelminth ProteinsProtein Subunit Vaccineschronic infectionimmunitynematodeType 2 immunityvaccinationwhipworm

Identifiers

PMID42815557
PMCPMC13626742

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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.