Evidence map›Paper›PMID 24657719›Full record

ArticleVaccine2014

Phase I clinical trial of O-acetylated pectin conjugate, a plant polysaccharide based typhoid vaccine.

Shousun C Szu, Kimi F-Y Lin, Steven Hunt, Chiayung Chu, Nguyen Duc Thinh

Registry-linked trialAbstract readClinical Trial, Phase I
In one paragraph

Article in Vaccine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00277147 (Salmonella Typhi Vi O-Acetyl Pectin-rEPA Conjugate Vaccine, Phase 1 Trial in Adults at NIH CC), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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.

NCT00277147 phase1completednot on this map

Salmonella Typhi Vi O-Acetyl Pectin-rEPA Conjugate Vaccine, Phase 1 Trial in Adults at NIH CC

TypeinterventionalSponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Ran2006 to 2008Enrolled25ConditionsTyphoid FeverArmsBB IND 6989
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Review
  3. Research Progress on the Anticancer Activity of Plant Polysaccharides.Recent patents on anti-cancer drug discovery · 2024
    Review
  4. Review
  5. Review
  6. Review
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

5 authors at 1 institution in 1 country.

Shousun C SzuEunice Kennedy Shriver, National Institute of Child Health & Human Development, National Institutes of Health, USA. Electronic address: Szus@mail.nih.gov.
Kimi F-Y LinEunice Kennedy Shriver, National Institute of Child Health & Human Development, National Institutes of Health, USA.
Steven HuntEunice Kennedy Shriver, National Institute of Child Health & Human Development, National Institutes of Health, USA.
Chiayung ChuEunice Kennedy Shriver, National Institute of Child Health & Human Development, National Institutes of Health, USA.
Nguyen Duc ThinhDivision of Food Safety, Department of Agriculture, Ho Chi Ming City, Viet Nam.
National Institutes of Health · US

Funding

Protein and Polysaccharide Conjugate Vaccines to enteric diseasesZIAHD001308 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI SZU, SHOUSUN C · 2009 to 2012
$1.9M
Intramural NIH HHS ZIA HD001308
6 · The paper itself

Abstract

backgroundTyphoid fever remains an important cause of morbidity and mortality in the developing countries. Vi capsular polysaccharide conjugate vaccine demonstrated safety and efficacy in young children in high endemic regions. A novel typhoid conjugate vaccine based on plant polysaccharide pectin was studied in a phase I trial.

methodsFruit pectin, having the same carbohydrate backbone structure as Vi, was purified from citrus peel and used as the polysaccharide source to prepare a semi-synthetic typhoid conjugate vaccine. Pectin was chemically O-acetylated (OAcPec) to antigenically resemble Vi and conjugated to carrier protein rEPA, a recombinant exoprotein A from Pseudomonas aeruginosa. 25 healthy volunteers, 18-45 years old, were injected once with OAcPec-rEPA. Safety and IgG antibodies reactive with Vi and pectin were analyzed.

resultsNo vaccine associated serious adverse reaction was reported. Six weeks after the injection of OAcPec-rEPA, 64% of the volunteers elicited >4-fold rise of anti-Vi IgG. At 26 weeks the level declined, but the difference between the levels at 6 and 26 weeks are not statistically significant. There is a direct correlation between the level of anti-Vi IgG before and after the injection (R(2)=0.96). The anti-Vi IgG can be absorbed by Vi, but not by pectin. There was no corresponding increase of anti-pectin after the injection, indicating the antibody response to OAcPec-rEPA was specific to Vi. There is no Vi-rEPA data in US adults for comparison of immune responses. The OAcPec-rEPA elicited significantly less IgG anti-Vi in US adults than those by Vi-rEPA in Vietnamese adults.

conclusionThe O-acetylated pectin conjugate, a plant based typhoid vaccine, is safe and immunogenic in adult volunteers. ClinicalTrial.gov identifier: NCT00277147, NIH Protocol ID number: OH06-CH-0070, FDA BB Investigation New Drug (IND) number 6989.

Indexed as

AcetylationAdolescentAdultAntibodies, BacterialCitrusFemaleHumansImmunoglobulin GMalePectinsPolysaccharides, BacterialRecombinant ProteinsTyphoid FeverTyphoid-Paratyphoid VaccinesVaccines, ConjugateYoung AdultAntibodies, BacterialImmunoglobulin GPectinsPolysaccharides, BacterialRecombinant ProteinsTyphoid-Paratyphoid VaccinesVaccines, ConjugateVi polysaccharide vaccine, typhoidPhase I pectin-basedPlant polysaccharideSafety immunogenicitySemi-syntheticTyphoid conjugate vaccine

Identifiers

PMID24657719
PMCPMC4034380
OpenAlexW2007760951

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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.