Evidence map›Paper›PMID 19564375›Full record

ArticleInfection and immunity2009

Protection against intestinal amebiasis by a recombinant vaccine is transferable by T cells and mediated by gamma interferon.

Xiaoti Guo, Lisa Barroso, Steven M Becker, David M Lyerly, Thomas S Vedvick, Steven G Reed, William A Petri, Eric R Houpt

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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, 49 citations in OpenAlex.

  1. Immunogenicity and safety of anHuman vaccines & immunotherapeutics · 2024
    Article
  2. Review
  3. Optimizing a Multi-Component IntranasalFrontiers in immunology · 2021
    Article
  4. Evaluation of the PEJournal of immunology research · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Regulation of virulence of Entamoeba histolytica.Annual review of microbiology · 2014
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 4 institutions in 1 country.

Xiaoti GuoDivision of Infectious Diseases and International Health, Department of Internal Medicine, University of Virginia, Charlottesville, Virginia 22908, USA.
Lisa Barroso
Steven M Becker
David M Lyerly
Thomas S Vedvick
Steven G Reed
William A Petri
Eric R Houpt
Office of Infectious Diseases · USInfectious Disease Research Institute · USTechLab (United States) · USUniversity of Virginia · US

Funding

UVA Digestive Health Research CenterP30DK067629 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PIZARRO, THERESA TORRES · 2004 to 2008
$5.6M
Cooperative Research Partnership for an Amebic Colitis VaccineU01AI070384 · NIAID · UNIVERSITY OF VIRGINIA · PI PETRI, WILLIAM A · 2006 to 2010
$4.1M
Mouse Strain dependent innate resistance to intestinal amebiasisR01AI071373 · NIAID · UNIVERSITY OF VIRGINIA · PI HOUPT, ERIC R · 2006 to 2009
$1.5M
NIAID NIH HHS R01 AI071373NIAID NIH HHS U01 AI070384NIDDK NIH HHS P30 DK067629
6 · The paper itself

Abstract

We have previously shown that vaccination with purified Entamoeba histolytica Gal/GalNAc lectin or recombinant subunits can protect mice from intestinal amebiasis upon intracecal challenge. In this study, we demonstrated with adoptive-transfer experiments that this lectin vaccine protection is mediated by T cells but not serum. The cell-mediated immune (CMI) response was characterized by significant gamma interferon (IFN-gamma), interleukin 12 (IL-12), IL-2, IL-10, and IL-17 production. To move toward a human vaccine, we switched to a recombinant protein and tested a range of adjuvants and routes appropriate for humans. We found that subcutaneous delivery of LecA with IDRI's adjuvant system EM014 elicited a potent Th1-type CMI profile and provided significant protection, as measured by culture negativity (79% efficacy); intranasal immunization with cholera toxin provided 56% efficacy; and alum induced a Th2-type response that protected 62 to 68% of mice. Several antibody and CMI cytokine responses were examined for correlates of protection, and prechallenge IFN-gamma(+) or IFN-gamma-, IL-2-, and tumor necrosis factor alpha-triple-positive CD4 cells in blood were statistically associated with protection. To test the role of IFN-gamma in LecA-mediated protection, we neutralized IFN-gamma in LecA-immunized mice and found that it abrogated the protection conferred by vaccination. These data demonstrate that CMI is sufficient for vaccine protection from intestinal amebiasis and reveal an important role for IFN-gamma, even in the setting of alum.

Indexed as

Adhesins, BacterialAdjuvants, ImmunologicAdoptive TransferAnimalsAntibodies, ProtozoanAntigens, Tumor-Associated, CarbohydrateDysentery, AmebicEntamoeba histolyticaInterferon-gammaMaleMiceMice, Inbred CBAProtozoan VaccinesT-LymphocytesVaccines, SyntheticAdhesins, BacterialAdjuvants, ImmunologicAntibodies, ProtozoanAntigens, Tumor-Associated, CarbohydrateInterferon-gammaLecA protein, bacteriaProtozoan VaccinesThomsen-Friedenreich antigenVaccines, Synthetic

Identifiers

PMID19564375
PMCPMC2738017
OpenAlexW2167674654

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.