Evidence map›Paper›PMID 22829921›Full record

ArticlePloS one2012

Glucopyranosyl Lipid Adjuvant (GLA), a Synthetic TLR4 agonist, promotes potent systemic and mucosal responses to intranasal immunization with HIVgp140.

Mauricio A Arias, Griet A Van Roey, John S Tregoning, Magdalini Moutaftsi, Rhea N Coler, Hillarie P Windish, Steven G Reed, Darrick Carter, Robin J Shattock

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 92 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Article
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  8. Toll-like receptor agonists as cancer vaccine adjuvants.Human vaccines & immunotherapeutics · 2024
    Review
  9. Article
  10. Vaccines · 2023
    Article
  11. Review
  12. Progress towards Adjuvant Development: Focus on Antiviral Therapy.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Developments in Vaccine Adjuvants.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

4 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

9 authors at 2 institutions in 2 countries.

Mauricio A AriasCentre for Infection and Immunity, St. George's University of London, London, United Kingdom.
Griet A Van Roey
John S Tregoning
Magdalini Moutaftsi
Rhea N Coler
Hillarie P Windish
Steven G Reed
Darrick Carter
Robin J Shattock
Infectious Disease Research Institute · USSt George's, University of London · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Successful vaccine development against HIV will likely require the induction of strong, long-lasting humoral and cellular immune responses in both the systemic and mucosal compartments. Based on the known immunological linkage between the upper-respiratory and urogenital tracts, we explored the potential of nasal adjuvants to boost immunization for the induction of vaginal and systemic immune responses to gp140. Mice were immunized intranasally with HIV gp140 together with micellar and emulsion formulations of a synthetic TLR4 agonist, Glucopyranosyl Lipid Adjuvant (GLA) and responses were compared to R848, a TLR7/8 agonist, or chitosan, a non TLR adjuvant. GLA and chitosan but not R848 greatly enhanced serum immunoglobulin levels when compared to antigen alone. Both GLA and chitosan induced high IgG and IgA titers in nasal and vaginal lavage and feces. The high IgA and IgG titers in vaginal lavage were associated with high numbers of gp140-specific antibody secreting cells in the genital tract. Whilst both GLA and chitosan induced T cell responses to immunization, GLA induced a stronger Th17 response and chitosan induced a more Th2 skewed response. Our results show that GLA is a highly potent intranasal adjuvant greatly enhancing humoral and cellular immune responses, both systemically and mucosally.

Indexed as

Adjuvants, ImmunologicAdministration, IntranasalAnimalsenv Gene Products, Human Immunodeficiency VirusFemaleMiceMice, Inbred BALB CMice, Inbred C57BLNasal MucosaToll-Like Receptor 4Adjuvants, Immunologicenv Gene Products, Human Immunodeficiency Virusgp140 envelope protein, Human immunodeficiency virus 1Tlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID22829921
PMCPMC3400629
OpenAlexW1983042902

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.