Evidence map›Paper›PMID 23142647›Full record

ReviewMicrobial pathogenesis2013

New technologies in developing recombinant attenuated Salmonella vaccine vectors.

Shifeng Wang, Qingke Kong, Roy Curtiss

Open access · greenAbstract readReview
In one paragraph

Review in Microbial pathogenesis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Recombinant AttenuatedVaccines · 2023
    Article
  10. Article
  11. Oral Immunization with AttenuatedMicrobiology spectrum · 2022
    Article
  12. Article
  13. Protective immunity enhancedFrontiers in immunology · 2022
    Article
  14. Non-Antibiotics Strategies to ControlAnimals : an open access journal from MDPI · 2022
    Review
  15. Review
  16. Article
  17. Optimized AttenuatedFrontiers in microbiology · 2021
    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

3 authors at 1 institution in 1 country.

Shifeng WangCenter for Infectious Diseases and Vaccinology, The Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287-5401, USA.
Qingke Kong
Roy Curtiss
Arizona State University · US

Funding

Recombinant Attenuated Salmonella Vaccines for HumansR01AI056289 · NIAID · WASHINGTON UNIVERSITY · PI CLARK-CURTISS, JOSEPHINE E, CURTISS III, ROY · 2003 to 2018
$5.8M
Recombinant Attenuated Bacterial Vaccines Against Biodefense AgentsR01AI093348 · NIAID · UNIVERSITY OF FLORIDA · PI CURTISS III, ROY · 2011 to 2015
$5.0M
Salmonella Vaccines Against Bacterial EnteropathogensR01AI060557 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CURTISS III, ROY · 2010 to 2014
$2.2M
NIAID NIH HHS R01 AI056289NIAID NIH HHS R01 AI060557NIAID NIH HHS R01 AI093348
6 · The paper itself

Abstract

Recombinant attenuated Salmonella vaccine (RASV) vectors producing recombinant gene-encoded protective antigens should have special traits. These features ensure that the vaccines survive stresses encountered in the gastrointestinal tract following oral vaccination to colonize lymphoid tissues without causing disease symptoms and to result in induction of long-lasting protective immune responses. We recently described ways to achieve these goals by using regulated delayed in vivo attenuation and regulated delayed in vivo antigen synthesis, enabling RASVs to efficiently colonize effector lymphoid tissues and to serve as factories to synthesize protective antigens that induce higher protective immune responses. We also developed some additional new strategies to increase vaccine safety and efficiency. Modification of lipid A can reduce the inflammatory responses without compromising the vaccine efficiency. Outer membrane vesicles (OMVs) from Salmonella-containing heterologous protective antigens can be used to increase vaccine efficiency. A dual-plasmid system, possessing Asd+ and DadB+ selection markers, each specifying a different protective antigen, can be used to develop multivalent live vaccines. These new technologies have been adopted to develop a novel, low-cost RASV synthesizing multiple protective pneumococcal protein antigens that could be safe for newborns/infants and induce protective immunity to diverse Streptococcus pneumoniae serotypes after oral immunization.

Indexed as

Drug CarriersGenetic VectorsAntigens, BacterialDrug DiscoveryGene Expression Regulation, BacterialHumansLipid APneumococcal VaccinesRecombinant ProteinsSalmonellaSecretory VesiclesStreptococcus pneumoniaeVaccines, AttenuatedVaccines, SyntheticAntigens, BacterialDrug CarriersLipid APneumococcal VaccinesRecombinant ProteinsVaccines, AttenuatedVaccines, Synthetic

Identifiers

PMID23142647
PMCPMC3587120
OpenAlexW2016812498

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.