Evidence map›Paper›PMID 26248044›Full record

ArticlePloS one2015

Production of a Shigella sonnei Vaccine Based on Generalized Modules for Membrane Antigens (GMMA), 1790GAHB.

Christiane Gerke, Anna Maria Colucci, Carlo Giannelli, Silvia Sanzone, Claudia Giorgina Vitali, Luigi Sollai, Omar Rossi, Laura B Martin, Jochen Auerbach, Vito Di Cioccio and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 6% of its field
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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 166 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  10. Development of a Promising Bivalent Vaccine AgainstExploration (Beijing, China) · 2025
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  11. Review
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  18. Article
  19. Immunogenicity evaluation of altSonflex1-2-3Frontiers in immunology · 2025
    Article
  20. Review

49 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Christiane GerkeSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Anna Maria ColucciSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Carlo GiannelliSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Silvia SanzoneSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Claudia Giorgina VitaliNovartis Vaccines and Diagnostics, S.r.l., Siena, Italy.
Luigi SollaiSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Omar RossiSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Laura B MartinSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Jochen AuerbachSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Vito Di CioccioSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Allan SaulSclavo Behring Vaccines Institute for Global Health S.r.l., Siena, Italy.
Toscana Life Sciences · ITNovartis (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we developed a high yield production process for outer membrane particles from genetically modified bacteria, called Generalized Modules of Membrane Antigens (GMMA), and the corresponding simple two step filtration purification, enabling economic manufacture of these particles for use as vaccines. Using a Shigella sonnei strain that was genetically modified to produce penta-acylated lipopolysaccharide (LPS) with reduced endotoxicity and to maintain the virulence plasmid encoding for the immunodominant O antigen component of the LPS, scale up of the process to GMP pilot scale was straightforward and gave high yields of GMMA with required purity and consistent results. GMMA were formulated with Alhydrogel and were highly immunogenic in mice and rabbits. In mice, a single immunization containing 29 ng protein and 1.75 ng of O antigen elicited substantial anti-LPS antibody levels. As GMMA contain LPS and lipoproteins, assessing potential reactogenicity was a key aspect of vaccine development. In an in vitro monocyte activation test, GMMA from the production strain showed a 600-fold lower stimulatory activity than GMMA with unmodified LPS. Two in vivo tests confirmed the low potential for reactogenicity. We established a modified rabbit pyrogenicity test based on the European Pharmacopoeia pyrogens method but using intramuscular administration of the full human dose (100 μg of protein). The vaccine elicited an average temperature rise of 0.5°C within four hours after administration, which was considered acceptable and showed that the test is able to detect a pyrogenic response. Furthermore, a repeat dose toxicology study in rabbits using intramuscular (100 μg/dose), intranasal (80 μg/dose), and intradermal (10 μg/dose) administration routes showed good tolerability of the vaccine by all routes and supported its suitability for use in humans. The S. sonnei GMMA vaccine is now in Phase 1 dose-escalation clinical trials.

Indexed as

AnimalsAntibodies, BacterialDysentery, BacillaryEnzyme-Linked Immunosorbent AssayHumansImmunoglobulin GInterleukin-6Leukocytes, MononuclearLipopolysaccharidesMiceMice, Inbred BALB CMonocytesO AntigensRabbitsShigella sonneiVaccines, SyntheticAntibodies, BacterialImmunoglobulin GInterleukin-6LipopolysaccharidesO AntigensVaccines, Synthetic

Identifiers

PMID26248044
PMCPMC4527750
OpenAlexW1085173720

What OpenQuestion holds

Textmetadata
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.