Evidence map›Paper›PMID 11179334›Full record

ArticleInfection and immunity2001

Intranasal immunization with SAG1 and nontoxic mutant heat-labile enterotoxins protects mice against Toxoplasma gondii.

C Bonenfant, I Dimier-Poisson, F Velge-Roussel, D Buzoni-Gatel, G Del Giudice, R Rappuoli, D Bout

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Comprehensive Overview ofPathogens (Basel, Switzerland) · 2021
    Review
  4. Review
  5. Targeted Delivery ofFrontiers in immunology · 2018
    Article
  6. Article
  7. RecombinantFrontiers in cellular and infection microbiology · 2017
    Article
  8. Recent advances in Toxoplasma gondii immunotherapeutics.The Korean journal of parasitology · 2014
    Review
  9. Possible link between Toxoplasma gondii and the anosmia associated with neurodegenerative diseases.American journal of Alzheimer's disease and other dementias · 2014
    Review
  10. Article
  11. Article
  12. Article
  13. Article
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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.

C BonenfantFaculté des Sciences Pharmaceutiques, UMR Université-INRA d'Immunologie Parasitaire, 37200 Tours, France.
I Dimier-Poisson
F Velge-Roussel
D Buzoni-Gatel
G Del Giudice
R Rappuoli
D Bout
Université de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective protection against intestinal pathogens requires both mucosal and systemic immune responses. Intranasal administration of antigens induces these responses but generally fails to trigger a strong protective immunity. Mucosal adjuvants can significantly enhance the immunogenicities of intranasally administered antigens. Cholera toxin (CT) and heat-labile enterotoxin (LT) are strong mucosal adjuvants with a variety of antigens. Moreover, the toxicities of CT and LT do not permit their use in humans. Two nontoxic mutant LTs, LTR72 and LTK63, were tested with Toxoplasma gondii SAG1 protein in intranasal vaccination of CBA/J mice. Vaccination with SAG1 plus LTR72 or LTK63 induced strong systemic (immunoglobulin G [IgG]) and mucosal (IgA) humoral responses. Splenocytes and mesenteric lymph node cells from mice immunized with LTR72 plus SAG1, but not those from mice immunized with LTK63 plus SAG1, responded to restimulation with a T. gondii lysate antigen in vitro. Gamma interferon and interleukin 2 (IL-2) production by splenocytes and IL-2 production by mesenteric lymph node cells were observed in vitro after antigen restimulation, underlying a Th1-like response. High-level protection as assessed by the decreased load of cerebral cysts after a challenge with the 76K strain of T. gondii was obtained in the group immunized with LTR72 plus SAG1 and LTK63 plus SAG1. They were as well protected as the mice immunized with the antigen plus native toxins. This is the first report showing protection against a parasite by using combinations of nontoxic mutant LTs and SAG1 antigen. These nontoxic mutant LTs are now attractive candidates for the development of mucosally delivered vaccines.

Indexed as

Antigens, ProtozoanEscherichia coli ProteinsVaccinationAdjuvants, ImmunologicAdministration, IntranasalAnimalsAntibodies, ProtozoanAntibody SpecificityBacterial ToxinsCytokinesEnterotoxinsFemaleImmunoglobulin AImmunoglobulin GIntestinesLungAdjuvants, ImmunologicAntibodies, ProtozoanAntigens, ProtozoanBacterial ToxinsCytokinesEnterotoxinsEscherichia coli Proteinsheat-labile enterotoxin, E coliImmunoglobulin AImmunoglobulin GProtozoan ProteinsProtozoan VaccinesSAG1 antigen, Toxoplasma

Identifiers

PMID11179334
PMCPMC98063
OpenAlexW2120482236

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.