Evidence map›Paper›PMID 20370633›Full record

ReviewCritical reviews in immunology2010

New technologies in using recombinant attenuated Salmonella vaccine vectors.

Roy Curtiss, Wei Xin, Yuhua Li, Wei Kong, Soo-Young Wanda, Bronwyn Gunn, Shifeng Wang

Abstract readReview
In one paragraph

Review in Critical reviews in immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 100 citations in OpenAlex.

  1. Virulence Reduction inBiomolecules · 2025
    Article
  2. Genetic engineering ofEcoSal Plus · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Refined control of CRISPR-Cas9 gene editing inFrontiers in immunology · 2023
    Article
  9. RecombinantAntibiotics (Basel, Switzerland) · 2022
    Review
  10. Protective immunity enhancedFrontiers in immunology · 2022
    Article
  11. Oral immunization of rat with chromosomal expression LipL32 in attenuatedClinical and experimental vaccine research · 2021
    Article
  12. Synthesis and delivery ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. AttenuatedVirulence · 2019
    Article
  15. Regulated DelayedTheranostics · 2019
    Article
  16. Oral Treatments With Probiotics and LiveFrontiers in microbiology · 2019
    Article
  17. Article
  18. Article
  19. Evaluation of Recombinant AttenuatedFrontiers in immunology · 2017
    Article
  20. 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

7 authors at 1 institution in 1 country.

Roy CurtissThe Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, Arizona 85287-5401, USA. rcurtiss@asu.edu
Wei Xin
Yuhua Li
Wei Kong
Soo-Young Wanda
Bronwyn Gunn
Shifeng Wang
Arizona State University · US

Funding

Salmonella Vaccines Against Bacterial EnteropathogensR01AI060557 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CURTISS III, ROY · 2010 to 2014
$2.2M
NIAID NIH HHS R01 AI060557
6 · The paper itself

Abstract

Recombinant attenuated Salmonella vaccines (RASVs) have been constructed to deliver antigens from other pathogens to induce immunity to those pathogens in vaccinated hosts. The attenuation means should ensure that the vaccine survives following vaccination to colonize lymphoid tissues without causing disease symptoms. This necessitates that attenuation and synthesis of recombinant gene encoded protective antigens do not diminish the ability of orally administered vaccines to survive stresses encountered in the gastrointestinal tract. We have eliminated these problems by using RASVs with regulated delayed expression of attenuation and regulated delayed synthesis of recombinant antigens. These changes result in RASVs that colonize effector lymphoid tissues efficiently to serve as "factories" to synthesize protective antigens that induce higher protective immune responses than achieved when using previously constructed RASVs. We have devised a biological containment system with regulated delayed lysis to preclude RASV persistence in vivo and survival if excreted. Attributes were added to reduce the mild diarrhea sometimes experienced with oral live RASVs and to ensure complete safety in newborns. These collective technologies have been used to develop a novel, low-cost, RASV-synthesizing, multiple-protective Streptococcus pneumoniae antigens that will be safe for newborns/infants and will induce protective immunity to diverse S. pneumoniae serotypes after oral immunization.

Indexed as

DNA, RecombinantDrug-Related Side Effects and Adverse ReactionsGenetic VectorsHumansSalmonella VaccinesStreptococcus pneumoniaeVaccines, AttenuatedDNA, RecombinantSalmonella VaccinesVaccines, Attenuated

Identifiers

PMID20370633
PMCPMC3970581
OpenAlexW1998362639

What OpenQuestion holds

Textmetadata
LicenceTDM
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.