Evidence map›Paper›PMID 19563890›Full record

ArticleVaccine2009

Transcutaneous immunization with a synthetic hexasaccharide-protein conjugate induces anti-Vibrio cholerae lipopolysaccharide responses in mice.

Julianne E Rollenhagen, Anuj Kalsy, Rina Saksena, Alaullah Sheikh, Mohammad Murshid Alam, Firdausi Qadri, Stephen B Calderwood, Pavol Kovác, Edward T Ryan

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Virus-like Particle Display ofACS infectious diseases · 2022
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  17. Production of Egg Yolk Antibody (IgY) AgainstAvicenna journal of medical biotechnology
    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

9 authors at 4 institutions in 2 countries.

Julianne E RollenhagenDivision of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02114, USA. julianne.rollenhagen@med.navy.mil
Anuj Kalsy
Rina Saksena
Alaullah Sheikh
Mohammad Murshid Alam
Firdausi Qadri
Stephen B Calderwood
Pavol Kovác
Edward T Ryan
International Centre for Diarrhoeal Disease Research · BDMassachusetts General Hospital · USNational Institutes of Health · USHarvard University · US

Funding

Reactions And Immunochemistry Of CarbohydratesZIADK059701 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI KOVAC, PAVOL · 2009 to 2019
$9.5M
Protecutive immunity to human cholera in BangladeshU01AI058935 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI CALDERWOOD, STEPHEN B., RYAN, EDWARD T. · 2003 to 2014
$7.8M
Training program in vaccine development and public healthD43TW005572 · FIC · MASSACHUSETTS GENERAL HOSPITAL · PI QADRI, FIRDAUSI, RYAN, EDWARD T. · 2000 to 2025
$5.4M
Mucosal Immunity to Antigens Expressed by V.choleraeR01AI040725 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RYAN, EDWARD T. · 1997 to 2006
$2.5M
Transcutaneous and oral-transcutaneous cholera immunization with TcpA and Peru15R21AI067342 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RYAN, EDWARD T. · 2007 to 2008
$365k
FIC NIH HHS D43 TW005572FIC NIH HHS TW05572NIAID NIH HHS AI058935NIAID NIH HHS AI067342NIAID NIH HHS AI40725NIAID NIH HHS R01 AI040725NIAID NIH HHS R21 AI067342NIAID NIH HHS U01 AI058935
6 · The paper itself

Abstract

Antibodies specific for Vibrio cholerae lipopolysaccaride (LPS) are common in humans recovering from cholera, and constitute a primary component of the vibriocidal response, a serum complement-mediated bacteriocidal response correlated with protection against cholera. In order to determine whether transcutaneous immunization (TCI) with a V. cholerae neoglycoconjugate (CHO-BSA) comprised of a synthetic terminal hexasaccharide of the O-specific polysaccharide of V. cholerae O1 (Ogawa) conjugated with bovine serum albumin (BSA) could induce anti-V. cholerae LPS and vibriocidal responses, we applied CHO-BSA transcutaneously in the presence or absence of the immune adjuvant cholera toxin (CT) to mice. Transcutaneously applied neoglycoconjugate elicited prominent V. cholerae specific LPS IgG responses in the presence of CT, but not IgM or IgA responses. CT applied on the skin induced strong IgG and IgA serum responses. TCI with neoglycoconjugate did not elicit detectable vibriocidal responses, protection in a mouse challenge assay, or stool anti-V. cholerae IgA responses, irrespective of the presence or absence of CT. Our results suggest that transcutaneously applied synthetic V. cholerae neoglycoconjugate is safe and immunogenic, but predominantly induces systemic LPS responses of the IgG isotype.

Indexed as

Adjuvants, ImmunologicAdministration, CutaneousAnimalsAntibodies, BacterialCholera ToxinCholera VaccinesImmunoglobulin AImmunoglobulin GMiceMice, Inbred BALB CMicrobial ViabilityO AntigensSerum Albumin, BovineVaccines, ConjugateVaccines, SyntheticVibrio choleraeAdjuvants, ImmunologicAntibodies, BacterialCholera ToxinCholera VaccinesImmunoglobulin AImmunoglobulin GO AntigensSerum Albumin, BovineVaccines, ConjugateVaccines, Synthetic

Identifiers

PMID19563890
PMCPMC2761657
OpenAlexW2119615067

What OpenQuestion holds

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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.