Evidence map›Paper›PMID 42566513›Full record

ArticleScience advances2026

ZPY-CpG-Ch, a broad coverage vaccine against

Teerawit Audshasai, Stavros Panagiotou, Lisa Crossman, Rong Xu, Lynn Verheijen, Chrispin Chaguza, Marie O'Brien, Aras Kadioglu

Abstract read
In one paragraph

Article in Science advances, 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

8 authors.

Teerawit AudshasaiDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0009-0008-0773-7685
Stavros PanagiotouDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0000-0001-9972-5068
Lisa CrossmanSequenceAnalysis.co.uk, Norwich Research Park, Norwich NR4 7UG, UK.ORCID 0000-0003-2390-4750
Rong XuDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0009-0005-8895-0303
Lynn VerheijenDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0009-0000-6492-6708
Chrispin ChaguzaHost-Microbe Interactions Dept. at St Jude Children's Research Hospital, Danny Thomas Place, Memphis, TN 38105, USA.ORCID 0000-0002-2108-1757
Marie O'BrienDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0000-0003-3104-2150
Aras KadiogluDepartment of Clinical Infection Microbiology & Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, The Ronald Ross Building, 8 West Derby St., Liverpool L69 7BE, UK.ORCID 0000-0003-1137-6321

Funding

Wellcome Trust
6 · The paper itself

Abstract

Existing licensed pneumococcal vaccines, including Prevnar-13 and its higher-valency successors, have played a major role in reducing invasive pneumococcal disease worldwide. However, their effectiveness is increasingly threatened by the rise of multidrug-resistant strains and the shift in circulating serotypes toward those not targeted by current vaccines-a trend known as serotype replacement. These evolving challenges underscore the urgent need for next-generation vaccines with broader, serotype-independent protection-long considered the holy grail of pneumococcal vaccine development. Here, we report the discovery and preclinical evaluation of ZPY-CpG-Ch, a broad-coverage protein-based pneumococcal vaccine formulation. We assessed the protective efficacy and immunogenicity of ZPY-CpG-Ch in translational murine models, using both adult and neonatal mice, and tested various adjuvants, protein combinations, and doses, followed by challenge experiments with both vaccine- and non-vaccine-covered serotypes. Prevnar-13 was included as a benchmark. While Prevnar-13

Indexed as

Pneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeAnimalsAntibodies, BacterialFemaleMiceProtein Subunit VaccinesSerogroupAntibodies, BacterialPneumococcal VaccinesProtein Subunit Vaccines

Identifiers

PMID42566513
PMCPMC13450215

What OpenQuestion holds

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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.