Evidence map›Paper›PMID 12941918›Full record

ArticleJournal of virology2003

Enhanced mucosal immunoglobulin A response of intranasal adenoviral vector human immunodeficiency virus vaccine and localization in the central nervous system.

Franck Lemiale, Wing-pui Kong, Levent M Akyürek, Xu Ling, Yue Huang, Bimal K Chakrabarti, Michael Eckhaus, Gary J Nabel

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

72 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
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  10. Anti-coronavirus vaccines will not accelerate the transition of humanity to a non-pandemic period, but the pandemic will take fewer victims.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Mucosal vaccines and technology.Clinical and experimental immunology · 2019
    Review
  18. Review
  19. Article
  20. Article

12 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Franck LemialeVaccine Research Center, NIAID/National Institutes of Health, MSC 3005, 40 Convent Drive, Bethesda, MD 20892-3005, USA.
Wing-pui Kong
Levent M Akyürek
Xu Ling
Yue Huang
Bimal K Chakrabarti
Michael Eckhaus
Gary J Nabel
Institut de Recherche Vaccinale · FRNational Heart Lung and Blood Institute · USOffice of Research Services · US

Funding

Recombinant Adenovirus Vector Vaccine StudiesZIAAI005001 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MASCOLA, JOHN · 2009 to 2014
$8.7M
Recombinant Adenovirus Vector Vaccine StudiesZ01AI005001 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI NABEL, GARY J · 2002 to 2008
$2.0M
6 · The paper itself

Abstract

Replication-defective adenovirus (ADV) vectors represent a promising potential platform for the development of a vaccine for AIDS. Although this vector is typically administered intramuscularly, it would be desirable to induce mucosal immunity by delivery through alternative routes. In this study, the immune response and biodistribution of ADV vectors delivered by different routes were evaluated. ADV vectors expressing human immunodeficiency virus type 1 (HIV-1) Gag, Pol, and Env were delivered intramuscularly or intranasally into mice. Intranasal immunization induced greater HIV-specific immunoglobulin A (IgA) responses in mucosal secretions and sera than in animals with intramuscular injection, which showed stronger systemic cellular and IgG responses. Administration of the vaccine through an intranasal route failed to overcome prior ADV immunity. Animals exposed to ADV prior to vaccination displayed substantially reduced cellular and humoral immune responses to HIV antigens in both groups, though the reduction was greater in animals immunized intranasally. This inhibition was partially overcome by priming with a DNA expression vector expressing HIV-1 Gag, Pol, and Env before boosting with the viral vector. Biodistribution of recombinant adenovirus (rADV) vectors administered intranasally revealed infection of the central nervous system, specifically in the olfactory bulb, possibly via retrograde transport by olfactory neurons in the nasal epithelium, which may limit the utility of this route of delivery of ADV vector-based vaccines.

Indexed as

AdenoviridaeAdministration, IntranasalAIDS VaccinesAnimalsBrainCD8-Positive T-LymphocytesFemaleGenetic VectorsImmunizationImmunoglobulin A, SecretoryInjections, IntramuscularInterferon-gammaMiceMice, Inbred BALB CVaccines, DNAAIDS VaccinesImmunoglobulin A, SecretoryInterferon-gammaVaccines, DNA

Identifiers

PMID12941918
PMCPMC224584
OpenAlexW2143169626

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.