Evidence map›Paper›PMID 28463465›Full record

ReviewMicrobiology and immunology2017

Dendritic cell-targeting DNA-based nasal adjuvants for protective mucosal immunity to Streptococcus pneumoniae.

Kosuke Kataoka, Yoshiko Fukuyama, David E Briles, Tatsuro Miyake, Kohtaro Fujihashi

Open access · bronzeAbstract readReview
In one paragraph

Review in Microbiology and immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. B Cell Immunosenescence.Annual review of cell and developmental biology · 2020
    Review
  6. Review
  7. Article
  8. 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

5 authors at 2 institutions in 2 countries.

Kosuke KataokaDepartment of Preventive and Community Dentistry, Osaka Dental University, Hirakata, Osaka 573-1121, Japan.
Yoshiko FukuyamaDepartments of Pediatric Dentistry and Microbiology, Immunobiology Vaccine Center, Institute for Oral Health Research, University of Alabama at Birmingham, Birmingham, AL 35294-0007, USA.
David E BrilesDepartments of Pediatric Dentistry and Microbiology, Immunobiology Vaccine Center, Institute for Oral Health Research, University of Alabama at Birmingham, Birmingham, AL 35294-0007, USA.
Tatsuro MiyakeDepartment of Preventive and Community Dentistry, Osaka Dental University, Hirakata, Osaka 573-1121, Japan.
Kohtaro FujihashiDepartments of Pediatric Dentistry and Microbiology, Immunobiology Vaccine Center, Institute for Oral Health Research, University of Alabama at Birmingham, Birmingham, AL 35294-0007, USA.
University of Alabama at Birmingham · USOsaka Dental University · JP

Funding

Vaccine potential of the proline-rich domain of pneumococcal surface protein AR01AI118805 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRILES, DAVID E · 2015 to 2019
$1.8M
NALT-BASED ADJUVANTS FOR MUCOSAL IMMUNITY IN AGINGR01AG025873 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FUJIHASHI, KOHTARO · 2006 to 2010
$1.4M
NIAID NIH HHS R01 AI118805NIA NIH HHS R01 AG025873
6 · The paper itself

Abstract

To develop safe vaccines for inducing mucosal immunity to major pulmonary bacterial infections, appropriate vaccine antigens (Ags), delivery systems and nontoxic molecular adjuvants must be considered. Such vaccine constructs can induce Ag-specific immune responses that protect against mucosal infections. In particular, it has been shown that simply mixing the adjuvant with the bacterial Ag is a relatively easy means of constructing adjuvant-based mucosal vaccine preparations; the resulting vaccines can elicit protective immunity. DNA-based nasal adjuvants targeting mucosal DCs have been studied in order to induce Ag-specific mucosal and systemic immune responses that provide essential protection against microbial pathogens that invade mucosal surfaces. In this review, initially a plasmid encoding the cDNA of Flt3 ligand (pFL), a molecule that is a growth factor for DCs, as an effective adjuvant for mucosal immunity to pneumococcal infections, is introduced. Next, the potential of adding unmethylated CpG oligodeoxynucleotide and pFL together with a pneumococcal Ag to induce protection from pneumococcal infections is discussed. Pneumococcal surface protein A has been used as vaccine for restoring mucosal immunity in older persons. Further, our nasal pFL adjuvant system with phosphorylcholine-keyhole limpet hemocyanin (PC-KLH) has also been used in pneumococcal vaccine development to induce complete protection from nasal carriage by Streptococcus pneumoniae. Finally, the possibility that anti-PC antibodies induced by nasal delivery of pFL plus PC-KLH may play a protective role in prevention of atherogenesis and thus block subsequent development of cardiovascular disease is discussed.

Indexed as

Adjuvants, ImmunologicAdministration, IntranasalAnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsDendritic CellsDNA, ComplementaryHemocyaninsHumansImmunity, MucosalMembrane ProteinsOligodeoxyribonucleotidesPhosphorylcholinePneumococcal InfectionsPneumococcal VaccinesAdjuvants, ImmunologicAntibodies, BacterialAntigens, BacterialBacterial ProteinsCPG-oligonucleotideDNA, Complementaryflt3 ligand proteinHemocyaninskeyhole-limpet hemocyaninMembrane ProteinsOligodeoxyribonucleotidesPhosphorylcholinepneumococcal surface protein APneumococcal VaccinesVaccines, DNAdendritic cellsDNA-based adjuvantsnasal vaccinationStreptococcus pneumoniae

Identifiers

PMID28463465
PMCPMC5529118
OpenAlexW2611584938

What OpenQuestion holds

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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.