Evidence map›Paper›PMID 39455688›Full record

ArticleScientific reports2024

Outer membrane protein C is a protective and unique vaccine antigen against Shigella flexneri 3a.

Anna Jarząb, Anna Dąbrowska, Piotr Naporowski, Karina Krasna, Agnieszka Szmyt, Michał Świat, Krzysztof Pawlik, Danuta Witkowska, Edmund Ziomek, Andrzej Gamian

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Human vaccines & immunotherapeutics · 2026
    Review
  2. Review
  3. Article
  4. Outer membrane protein C (OMPC) epitope ofFrontiers in immunology · 2025
    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

10 authors.

Anna JarząbHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland. anna.jarzab@hirszfeld.pl.
Anna DąbrowskaDepartment of Animal Products Technology and Quality Management, Wroclaw University of Environmental and Life Sciences, Chelmonskiego Str. 37/41, 51-630, Wroclaw, Poland.
Piotr NaporowskiHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Karina KrasnaHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Agnieszka SzmytDepartment of Animal Products Technology and Quality Management, Wroclaw University of Environmental and Life Sciences, Chelmonskiego Str. 37/41, 51-630, Wroclaw, Poland.
Michał ŚwiatHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Krzysztof PawlikHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Danuta WitkowskaHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Edmund ZiomekHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.
Andrzej GamianHirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.

Funding

National Centre for Science and Development, Leader XIII Program 0093/L-13/2022
6 · The paper itself

Abstract

The anti-Shigella vaccine is one of the WHO's top priorities. Every year the disease kills more than 200,000 people worldwide and poses a serious threat to children under 5 years of age and the elderly. Increasing antibiotic resistance and limitations in diagnostics emphasize the need to develop an effective vaccine. Recent research and clinical trials report multiple approaches used in Shigella-vaccine development. However, despite the efforts of researchers, pharmaceutical companies and health care organizations, there is no licensed vaccine against shigellosis available to the community. Here, we expressed, broadly characterized and demonstrated the protective properties of outer membrane protein C as an effective molecule serving as a universal antigen for Shigella vaccine. Most of the current approaches to the development of Shigella vaccine are based on the polysaccharide antigens, which are serotype specific and have always been challenging in terms of their high specificity, targeting the most exposed surface antigens identified for certain Shigella serotypes. Here, we confirm immunogenic and protective properties of the recombinant OmpC protein, which protects mice against a lethal dose of a virulent strain 2 weeks after active immunization.

Indexed as

Antigens, BacterialDysentery, BacillaryShigella flexneriShigella VaccinesAnimalsAntibodies, BacterialBacterial Outer Membrane ProteinsFemaleHumansMiceMice, Inbred BALB CPorinsAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsOmpC proteinPorinsShigella VaccinesDiarrheaInfectious diseaseOmpCShigellaVaccine

Identifiers

PMID39455688
PMCPMC11511853

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.