Evidence map›Paper›PMID 33862589›Full record

Trial reportEBioMedicine2021

Human challenge study with a Shigella bioconjugate vaccine: Analyses of clinical efficacy and correlate of protection.

Kawsar R Talaat, Cristina Alaimo, Patricia Martin, A Louis Bourgeois, Anita M Dreyer, Robert W Kaminski, Chad K Porter, Subhra Chakraborty, Kristen A Clarkson, Jessica Brubaker and 9 more

3 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in EBioMedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 5% 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.

NCT02646371 phase2completednot on this map

Phase 2b, Double-blind, Placebo-controlled Efficacy Challenge Study With a Candidate Bioconjugate Vaccine Against Shigella Flexneri 2a

TypeinterventionalSponsorLimmaTech Biologics AGRan2015 to 2017Enrolled67ConditionsShigellosisArmsFlexyn2a, Placebo
NCT06523231 phase2completednot on this mapstarted 2025, after this paper: background citation

Safety and Immunogenicity of a Second Generation Shigella Bioconjugate Vaccine: a Phase II Randomized, Controlled, and Blinded Study in 9-month-old Infants

TypeinterventionalSponsorLimmaTech Biologics AGRan2025 to 2026Enrolled110ConditionsShigellosisArmsShigella4V2, MenACWY
NCT06615375 phase2active not recruitingnot on this mapstarted 2024, after this paper: background citation

Phase 2b, Double-blind, Placebo-controlled Efficacy Challenge Study With the Shigella Tetravalent Bioconjugate Vaccine Shigella4V2

TypeinterventionalSponsorLimmaTech Biologics AGRan2024 to 2026Enrolled120ConditionsShigellosisArmsShigella4V2, Placebo
3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Consequences of Shigella infection in young children: a systematic review.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2023
    Pooled it
  3. Threshold protective levels of serum IgG to Shigella lipopolysaccharide: re-analysis of Shigella vaccine trials data.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
    Trial
  4. Trial
  5. CRISPR-Cas12a assay for rapid and specific detection ofJournal of clinical microbiology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Causal Approaches to Disease Progression Analyses.Epidemiology (Cambridge, Mass.) · 2025
    Article
  11. Shigellosis.Lancet (London, England) · 2025
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 2 countries.

Kawsar R TalaatDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States. Electronic address: ktalaat@jhu.edu.
Cristina AlaimoLimmaTech Biologics AG, Schlieren, Switzerland.
Patricia MartinLimmaTech Biologics AG, Schlieren, Switzerland.
A Louis BourgeoisDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States; Now at PATH Center for Vaccine Innovation and Access, Washington, DC, United States.
Anita M DreyerLimmaTech Biologics AG, Schlieren, Switzerland.
Robert W KaminskiWalter Reed Army Institute of Research, Silver Spring, MD, United States.
Chad K PorterNaval Medical Research Center, Silver Spring, MD, United States.
Subhra ChakrabortyDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Kristen A ClarksonWalter Reed Army Institute of Research, Silver Spring, MD, United States.
Jessica BrubakerDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Daniel ElwoodDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Rahel FrölichLimmaTech Biologics AG, Schlieren, Switzerland.
Barbara DeNearingDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Hailey WeertsWalter Reed Army Institute of Research, Silver Spring, MD, United States.
Brittany L FeijooDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Jane HalpernDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
David SackDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Mark S RiddleNaval Medical Research Center, Silver Spring, MD, United States.
Veronica Gambillara FonckLimmaTech Biologics AG, Schlieren, Switzerland.
Johns Hopkins University · USSpital Limmattal · CHWalter Reed Army Institute of Research · USNaval Medical Research Command · USProgram for Appropriate Technology in Health · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundShigellosis is a major cause of moderate to severe diarrhoea and dysentery in children under 5 years of age in low and middle-income countries. The Flexyn2a vaccine conjugates the O-polysaccharide of Shigella flexneri 2a to Pseudomonas aeruginosa exotoxin A. We describe a Phase 2b proof-of-concept challenge study that evaluated safety, immunogenicity, and efficacy of the Flexyn2a vaccine to protect against shigellosis.

methodsIn this randomized, double blind, placebo-controlled trial, healthy adults were randomized 1:1 to receive Flexyn2a (10 µg) or placebo intramuscularly, twice, 4 weeks apart, followed by challenge 4 weeks later with 1500 colony forming units (CFUs) of S. flexneri 2a strain 2457T. The primary outcome was vaccine-induced protection. S. flexneri 2a lipopolysaccharide (LPS)-specific immune responses were assessed.

findingsSixty-seven subjects were enrolled, 34 received vaccine and 33 placebo. The vaccine was well tolerated; the majority of adverse events were mild in nature. Thirty vaccinees and 29 placebo recipients received the S. flexneri 2a challenge. Vaccination resulted in a 30.2% reduction in shigellosis compared with placebo (13/30 vs. 18/29; p = 0.11; 95% CI -15 to 62.6). Vaccine efficacy was more robust against severe disease, reaching 51.7% (p = 0.015, 95% CI 5.3 to 77.9) against moderate/severe diarrhoea or dysentery concurrent with fever or severe enteric symptoms and 72.4% (p = 0.07) against more severe diarrhoea (≥10 lose stools or ≥1000 g loose stools/24 h). Vaccinated subjects were less likely to need early antibiotic intervention following challenge (protective efficacy 51.7%, p = 0.01; 95% CI 9 to 76.8). In those who developed shigellosis, vaccinated subjects had a lower disease severity score (p = 0.002) than placebo-recipients. Additionally, LPS-specific serum IgG responses in Flexyn2a recipients were associated with protection against disease (p = 0.0016) and with a decreased shigellosis disease score (p = 0.002).

interpretationThe Flexyn2a bioconjugate vaccine was immunogenic, well tolerated and protected against severe illness after Shigella challenge and is a promising Shigella vaccine construct. We identified a strong association between anti-S. flexneri 2a serum IgG and a reduction in disease outcomes. (Clinicaltrials.gov, NCT02646371.)

fundingFunding for this study was through a grant from the Wellcome Trust.

Indexed as

AdultAntibodies, BacterialAntibody SpecificityDysentery, BacillaryFemaleHumansImmunoglobulin GLipopolysaccharidesMaleMiddle AgedShigellaShigella flexneriShigella VaccinesTreatment OutcomeVaccinationYoung AdultAntibodies, BacterialImmunoglobulin GLipopolysaccharidesShigella VaccinesBioconjugate vaccineControlled human challenge studyShigellaShigella flexneri 2aVaccine

Identifiers

PMID33862589
PMCPMC8054157
OpenAlexW3153742271

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.