Evidence map›Paper›PMID 40733680›Full record

ReviewVaccines2025

Recent Advances in Bioconjugate Vaccine Development.

Brendan W Wren, Catherine L Hall, Vanessa S Terra, Mark A Harrison, Elizabeth Atkins, Fauzy Nasher, Ian J Passmore

Abstract readReview
In one paragraph

Review in Vaccines, 2025. 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. Article
  2. Article
  3. 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

7 authors.

Brendan W WrenDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.ORCID 0000-0002-6140-9489
Catherine L HallDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.
Vanessa S TerraDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.ORCID 0000-0002-2734-4036
Mark A HarrisonDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.
Elizabeth AtkinsDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.ORCID 0000-0002-1783-6889
Fauzy NasherDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.ORCID 0000-0001-7368-3867
Ian J PassmoreDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, Keppel St, London WC1E 7HT, UK.ORCID 0000-0002-4418-6957

Funding

Biotechnology and Biological Sciences Research Council BB/W005816/1Biotechnology and Biological Sciences Research Council BB/W006146/1Biotechnology and Biological Sciences Research Council BB/Y008472/1Engineering and Physical Sciences Research Council EP/Y530542/1RIGHT Foundation RF-2023-V02Wellcome Trust 221589/Z/20/ZWellcome Trust 221803/Z/20/Z
6 · The paper itself

Abstract

Glycoconjugate vaccines, consisting of a protein component covalently linked to a glycan antigen, have led to a significant reduction in the global occurrence of bacterial meningitis and pneumonia. They provide robust, lasting immunity in all age groups. However, their production by traditional chemical conjugation approaches has drawbacks in terms of complexity, cost, and lack of flexibility in design, which explains their limited application to a few pathogenic bacteria in the past four decades. Protein glycan coupling technology (PGCT) or bioconjugation, where glycoconjugates are produced in purpose-engineered bacterial cells, is a useful alternative to chemical conjugation and promises an array of low-cost custom-made glycoconjugate vaccines with vast protein glycan combinations. The technology has undergone significant development since its inception, and new advances and refinements continually drive the field forward. Several bioconjugate vaccines are currently in clinical trials, demonstrating the potential of the technology. We will review the wide applicability of bioconjugation and recent developments in each of the components of the technology, namely, glycan expression, protein selection, and the coupling of selected glycan with proteins, all within custom-designed

Indexed as

bacterial vaccinesbioconjugationcarrier proteinsglycoconjugate vaccinespolysaccharidesprotein glycan coupling technology (PGCT)

Identifiers

PMID40733680
PMCPMC12300370

What OpenQuestion holds

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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.