Evidence map›Paper›PMID 26551346›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2016

PEG modified liposomes containing CRX-601 adjuvant in combination with methylglycol chitosan enhance the murine sublingual immune response to influenza vaccination.

Hardeep S Oberoi, Yvonne M Yorgensen, Audrey Morasse, Jay T Evans, David J Burkhart

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Strategies for fighting pandemic virus infections: Integration of virology and drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Liposomes used as a vaccine adjuvant-delivery system: From basics to clinical immunization.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Review
  16. Theranostics Aspects of Various Nanoparticles in Veterinary Medicine.International journal of molecular sciences · 2018
    Review
  17. Review
  18. Review
  19. Review
  20. Mucosal vaccine delivery: Current state and a pediatric perspective.Journal of controlled release : official journal of the Controlled Release Society · 2016
    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

5 authors at 1 institution in 1 country.

Hardeep S OberoiGSK Vaccines, 553 Old Corvallis Road, Hamilton, MT 59840, USA.
Yvonne M YorgensenGSK Vaccines, 553 Old Corvallis Road, Hamilton, MT 59840, USA.
Audrey MorasseGSK Vaccines, 525 Boulevard Cartier, Laval, QC H7V 3S8, Canada.
Jay T EvansGSK Vaccines, 553 Old Corvallis Road, Hamilton, MT 59840, USA.
David J BurkhartGSK Vaccines, 553 Old Corvallis Road, Hamilton, MT 59840, USA. Electronic address: david.j.burkhart@gsk.com.
GlaxoSmithKline (Switzerland) · CH

Funding

NIAID NIH HHS HHSN272200900008CPHS HHS HHSN272200900008C
6 · The paper itself

Abstract

The mucosa is the primary point of entry for pathogens making it an important vaccination site to produce a protective mucosal immune response. While the sublingual (SL) mucosa presents several barriers to vaccine penetration, its unique anatomy and physiology makes it one of the best options for mucosal vaccination. Efficient and directed delivery of adjuvants and antigens to appropriate immune mediators in the SL tissue will aid in development of effective SL vaccines against infectious diseases. Herein we demonstrate a robust immune response against influenza antigens co-delivered sublingually with engineered liposomes carrying the synthetic Toll-like receptor-4 agonist, CRX-601. Liposome modification with PEG copolymers (Pluronics), phospholipid-PEG conjugates and chitosan were evaluated for their ability to generate an immune response in a SL murine influenza vaccine model. Phospholipid-PEG conjugates were more effective than Pluronic copolymers in generating stable, surface neutral liposomes. SL vaccination with surface modified liposomes carrying CRX-601 adjuvant generated significant improvements in flu-specific responses compared with unmodified liposomes. Furthermore, the coating of modified liposomes with methylglycol chitosan produced the most effective flu-specific immune response. These results demonstrate efficient SL vaccine delivery utilizing a combination of a muco-adhesive and surface neutral liposomes to achieve a robust mucosal and systemic immune response.

Indexed as

Adjuvants, ImmunologicAdministration, SublingualAnimalsBody TemperatureChitosanFemaleGlucosephosphatesGlycolipidsImmunoglobulin AImmunoglobulin GInfluenza VaccinesLiposomesMice, Inbred BALB CPoloxamerPolyethylene GlycolsRabbitsAdjuvants, ImmunologicChitosanGlucosephosphatesGlycolipidsImmunoglobulin AImmunoglobulin GInfluenza VaccinesLiposomesmethylglycol chitosanPoloxamerPolyethylene GlycolsTlr4 protein, mouseToll-Like Receptor 4ChitosanInfluenzaLiposomesMucosalSublingualTLR4Vaccine

Identifiers

PMID26551346
PMCPMC4729458
OpenAlexW2124480779

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.