Evidence map›Paper›PMID 8945569›Full record

Trial reportInfection and immunity1996

Oral and rectal immunization of adult female volunteers with a recombinant attenuated Salmonella typhi vaccine strain.

D Nardelli-Haefliger, J P Kraehenbuhl, R Curtiss, F Schodel, A Potts, S Kelly, P De Grandi

Open access · bronzeAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in Infection and immunity, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
  2. Genetic engineering ofEcoSal Plus · 2024
    Review
  3. Review
  4. Article
  5. Plague Vaccines: Status and Future.Advances in experimental medicine and biology · 2016
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Plant-based oral vaccines: results of human trials.Current topics in microbiology and immunology · 2009
    Review
  13. Article
  14. Article
  15. Article
  16. Tolerance in the absence of autoantigen.Endocrine, metabolic & immune disorders drug targets · 2007
    Review
  17. Article
  18. Article
  19. Review
  20. Bacterial infectious disease control by vaccine development.The Journal of clinical investigation · 2002
    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

7 authors at 1 institution in 1 country.

D Nardelli-HaefligerDepartment of Gynecology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland. DNARDELL@ulrec1.unil.ch
J P Kraehenbuhl
R Curtiss
F Schodel
A Potts
S Kelly
P De Grandi
University Hospital of Lausanne · CH

Funding

ANTIGEN DELIVERY SYSTEM DESIGN FOR HOST DEFENSE ANALYSISR01DE006669 · NIDCR · WASHINGTON UNIVERSITY · PI CURTISS, ROY · 1985 to 2004
$1.6M
HEPATITIS B NUCLEOCPSID--MULTIVALENT IMMUNOLOGIC CARRIERR01AI033562 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI MILICH, DAVID R. · 1992 to 1995
–
NIAID NIH HHS AI 33562NIDCR NIH HHS DEO 6669
6 · The paper itself

Abstract

An attenuated strain of Salmonella typhi delta(cya) delta(crp-cdt) delta(asd) expressing a gene encoding a hepatitis B virus core-pre-S protein was tested in female adult volunteers for its ability to elicit a systemic and a mucosal immune response. Specifically, our purpose was to evaluate the potential of such a vaccine strain to induce specific secretory immunoglobulin A (sIgA) at genital and rectal surfaces. Oral and rectal routes of immunization were compared: oral immunization induced seroconversion against the bacterial lipopolysaccharide (LPS) in six out of seven volunteers, while after rectal immunization only one out of six volunteers seroconverted against LPS. To our disappointment, the latter volunteer was also the only one who seroconverted against the carried antigen (pre-S1), demonstrating the poor ability of this live vaccine to induce an immune response against the carried antigen. Anti-LPS sIgA was found in both the vaginal and cervical secretions of a volunteer who presented a strong seroconversion after oral immunization (16-fold increase in anti-LPS IgG). Smaller amounts of anti-LPS sIgA were found in the rectal secretions of one orally and one rectally immunized volunteer and in the saliva of three orally and one rectally immunized woman. Our data show for the first time that it is possible to induce specific sIgA in the genital and rectal tracts of women by using an S. typhi vaccine strain.

Indexed as

VaccinationAdministration, OralAdministration, RectalAdultFemaleGene ExpressionHepatitis B virusHumansSalmonella typhiTyphoid FeverVaccines, SyntheticViral Core ProteinsVaccines, SyntheticViral Core Proteins

Identifiers

PMID8945569
PMCPMC174511
OpenAlexW2137160891

What OpenQuestion holds

Textmetadata
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.