Evidence map›Paper›PMID 29655627›Full record

Trial reportVaccine2018

Lipopolysaccharide-specific memory B cell responses to an attenuated live cholera vaccine are associated with protection against Vibrio cholerae infection.

Douglas J Haney, Michael D Lock, Marc Gurwith, Jakub K Simon, Glenn Ishioka, Mitchell B Cohen, Beth D Kirkpatrick, Caroline E Lyon, Wilbur H Chen, Marcelo B Sztein and 2 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Vaccine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01895855 (A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Efficacy Trial of a Single Dose Live Oral Cholera Vaccine, PXVX0200 CVD 103-HgR, in Preventing Cholera Following Challenge With Vibrio Cholerae 10 Days or 3 Months After Vaccination), which is not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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.

NCT01895855 phase3completednot on this map

A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Efficacy Trial of a Single Dose Live Oral Cholera Vaccine, PXVX0200 CVD 103-HgR, in Preventing Cholera Following Challenge With Vibrio Cholerae 10 Days or 3 Months After Vaccination

TypeinterventionalSponsorBavarian NordicRan2013 to 2014Enrolled197ConditionsCholeraArmsPXVX0200, placebo
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Long-Term Kinetics of Serological Antibodies againstInternational journal of environmental research and public health · 2022
    Pooled it
  2. Frontiers in immunology · 2025
    Article
  3. Article
  4. Article
  5. A polyvalent multiepitope protein cross-protects againstProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. Correlates of Protection for Cholera.The Journal of infectious diseases · 2021
    Article
  8. Systemic, Mucosal, and Memory Immune Responses following Cholera.Tropical medicine and infectious disease · 2021
    Review
  9. Review
  10. An overview of VaxchoraHuman vaccines & immunotherapeutics · 2020
    Article
  11. mSphere · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Cholera: Immunity and Prospects in Vaccine Development.The Journal of infectious diseases · 2018
    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

12 authors at 5 institutions in 1 country.

Douglas J HaneyPaxVax, Inc., Redwood City, CA, United States. Electronic address: haney_doug@hotmail.com.
Michael D LockPaxVax, Inc., Redwood City, CA, United States.
Marc GurwithPaxVax, Inc., Redwood City, CA, United States.
Jakub K SimonPaxVax, Inc., Redwood City, CA, United States.
Glenn IshiokaPaxVax, Inc., Redwood City, CA, United States.
Mitchell B CohenUniversity of Alabama at Birmingham, Birmingham, AL, United States.
Beth D KirkpatrickVaccine Testing Center, University of Vermont, College of Medicine, Burlington, VT, United States.
Caroline E LyonVaccine Testing Center, University of Vermont, College of Medicine, Burlington, VT, United States.
Wilbur H ChenCenter for Vaccine Development (CVD), University of Maryland School of Medicine, Baltimore, MD, United States.
Marcelo B SzteinCenter for Vaccine Development (CVD), University of Maryland School of Medicine, Baltimore, MD, United States.
Myron M LevineCenter for Vaccine Development (CVD), University of Maryland School of Medicine, Baltimore, MD, United States.
Jason B HarrisDivision of Global Health, Massachusetts General Hospital for Children, Boston, MA, United States; Department of Pediatrics, Harvard Medical School, Cambridge, MA, United States. Electronic address: jbharris@mgh.harvard.edu.
PaxVax (United States) · USUniversity of Maryland, Baltimore · USUniversity of Vermont · USBoston Children's Hospital · USUniversity of Alabama at Birmingham · US

Funding

Wild-type S. typhi Infection in Humans: Integrated Immunoprotective MechanismsU19AI082655 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI GREENWALD, BRUCE D · 2009 to 2018
$27.8M
VERMONT IMMUNOBIOLOIGY/ INFECTIOUS DISEASES CENTERP20RR021905 · NCRR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HILL, JACK · 2006 to 2011
$14.5M
Vermont Immunology/Infectious Diseases CenterP30GM118228 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2016 to 2021
$6.8M
Innate and early B cell responses to V. choleraeR01AI103055 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI HARRIS, JASON B · 2014 to 2018
$3.9M
NCRR NIH HHS P20 RR021905NIAID NIH HHS R01 AI103055NIAID NIH HHS U19 AI082655NIGMS NIH HHS P30 GM118228
6 · The paper itself

Abstract

backgroundThe single-dose live attenuated vaccine CVD 103-HgR protects against experimental Vibrio cholerae infection in cholera-naïve adults for at least 6 months after vaccination. While vaccine-induced vibriocidal seroconversion is associated with protection, vibriocidal titers decline rapidly from their peak 1-2 weeks after vaccination. Although vaccine-induced memory B cells (MBCs) might mediate sustained protection in individuals without detectable circulating antibodies, it is unknown whether oral cholera vaccination induces a MBC response.

methodsIn a study that enrolled North American adults, we measured lipopolysaccharide (LPS)- and cholera toxin (CtxB)-specific MBC responses to PXVX0200 (derived from the CVD 103-HgR strain) and assessed stool volumes following experimental Vibrio cholerae infection. We then evaluated the association between vaccine-induced MBC responses and protection against cholera.

resultsThere was a significant increase in % CT-specific IgG, % LPS-specific IgG, and % LPS-specific IgA MBCs which persisted 180 days after vaccination as well as a significant association between vaccine-induced increase in % LPS-specific IgA MBCs and lower post-challenge stool volume (r = -0.56, p < 0.001). DISCUSSION: Oral cholera vaccination induces antigen-specific MBC responses, and the anamnestic LPS-specific responses may contribute to long-term protection and provide correlates of the duration of vaccine-induced protection. CLINICAL TRIALS REGISTRATION: NCT01895855.

Indexed as

Immunologic MemoryAdministration, OralAdultAntibodies, BacterialB-LymphocytesCholeraCholera ToxinCholera VaccinesHumansImmunoglobulin AImmunoglobulin GLipopolysaccharidesTime FactorsVaccines, AttenuatedVibrio cholerae O1Antibodies, BacterialCholera Toxincholera vaccine CVD 103-HgRCholera VaccinesImmunoglobulin AImmunoglobulin GLipopolysaccharidesVaccines, AttenuatedCholeraCholera-naïveCVD 103-HgRDuration of protectionLive vaccineMemory B cells

Identifiers

PMID29655627
PMCPMC5922764
OpenAlexW2797441468

What OpenQuestion holds

Textmetadata
LicenceTDM
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.