Evidence map›Paper›PMID 27402566›Full record

ArticleVaccine2016

Evaluation of novel synthetic TLR7/8 agonists as vaccine adjuvants.

Alyson J Smith, Yufeng Li, Hélène G Bazin, Julien R St-Jean, Daniel Larocque, Jay T Evans, Jory R Baldridge

Abstract readEvaluation Study
In one paragraph

Article in Vaccine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Peptide-based vaccine for cancer therapies.Frontiers in immunology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Protein-based nanoparticles in cancer vaccine development.Nanomedicine : nanotechnology, biology, and medicine · 2019
    Review
  19. Review
  20. Small-Molecule Targets in Tumor Immunotherapy.Natural products and bioprospecting · 2018
    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

7 authors at 1 institution in 1 country.

Alyson J SmithGSK Vaccines, Hamilton, MT 59840, USA. Electronic address: alyson.smith@mso.umt.edu.
Yufeng LiGSK Vaccines, Hamilton, MT 59840, USA.
Hélène G BazinGSK Vaccines, Hamilton, MT 59840, USA.
Julien R St-JeanGSK Vaccines, Hamilton, MT 59840, USA.
Daniel LarocqueGSK Vaccines, Hamilton, MT 59840, USA.
Jay T EvansGSK Vaccines, Hamilton, MT 59840, USA.
Jory R BaldridgeGSK Vaccines, Hamilton, MT 59840, USA.
GlaxoSmithKline (United States) · US

Funding

NIAID NIH HHS HHSN272200900036C
6 · The paper itself

Abstract

Small-molecule adjuvants that boost and direct adaptive immunity provide a powerful means to increase the effectiveness of vaccines. Through rational design several novel imidazoquinoline and oxoadenine TLR7/8 agonists, each with unique molecular modifications, were synthesized and assessed for their ability to augment adaptive immunity. All agonists bound human TLR7 and TLR8 and induced maturation of both human mDCs and pDCs. All agonists prompted production of type I interferon and/or proinflammatory cytokines, albeit with varying potencies. In most in vitro assays, the oxoadenine class of agonists proved more potent than the imidazoquinolines. Therefore, an optimized oxoadenine TLR7/8 agonist that demonstrated maximal activity in the in vitro assays was further assessed in a vaccine study with the CRM197 antigen in a porcine model. Antigen-specific antibody production was greatly enhanced in a dose dependent manner, with antibody titers increased 800-fold compared to titers from pigs vaccinated with the non-adjuvanted vaccine. Moreover, pigs vaccinated with antigen containing the highest dose of adjuvant promoted a 13-fold increase in the percentage of antigen-specific CD3(+)/CD8(+) T cells over pigs vaccinated with antigen alone. Together this work demonstrates the promise of these novel TLR7/8 agonists as effective human vaccine adjuvants.

Indexed as

Adaptive ImmunityAdjuvants, ImmunologicAnimalsCD8-Positive T-LymphocytesCytokinesDendritic CellsHumansImidazolesPyridinesQuinolinesSwineToll-Like Receptor 7Toll-Like Receptor 8VaccinesAdjuvants, ImmunologicCytokinesImidazolesoxoamidePyridinesQuinolinesToll-Like Receptor 7Toll-Like Receptor 8VaccinesAdjuvantsInnate immunityToll like 7/8 receptorsVaccines

Identifiers

PMID27402566
PMCPMC4968040
OpenAlexW2460044542

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.