Evidence map›Paper›PMID 20230025›Full record

ArticleMolecular pharmaceutics2010

In vitro analysis of acetalated dextran microparticles as a potent delivery platform for vaccine adjuvants.

Eric M Bachelder, Tristan T Beaudette, Kyle E Broaders, Jean M J Fréchet, Mark T Albrecht, Alfred J Mateczun, Kristy M Ainslie, John T Pesce, Andrea M Keane-Myers

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 128 citations in OpenAlex.

  1. Role of site-directed mutagenesis and adjuvants in the stability and potency of anthrax protective antigen.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Review
  2. Review
  3. Influenza Virus and SARS-CoV-2 Vaccines.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Review
  4. Polymeric Nanoparticle-Based Vaccine Adjuvants and Delivery Vehicles.Current topics in microbiology and immunology · 2021
    Review
  5. Formulation of host-targeted therapeutics against bacterial infections.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
  6. Review
  7. Biodegradable polymers for modern vaccine development.Journal of industrial and engineering chemistry (Seoul, Korea) · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 3 institutions in 1 country.

Eric M BachelderDepartment of Chemistry, University of California, Berkeley, California 94720-1460, USA.
Tristan T Beaudette
Kyle E Broaders
Jean M J Fréchet
Mark T Albrecht
Alfred J Mateczun
Kristy M Ainslie
John T Pesce
Andrea M Keane-Myers
The Ohio State University · USNaval Medical Research Command · USUniversity of California, Berkeley · US

Funding

Nanoscale delivery vehicles for antigen-based vaccinesR01EB005824 · NIBIB · UNIVERSITY OF CALIFORNIA BERKELEY · PI FRECHET, JEAN M · 2005 to 2008
$2.0M
NIBIB NIH HHS R01 EB005824NIBIB NIH HHS R01-EB005824
6 · The paper itself

Abstract

Toll-like receptor (TLR) agonists induce potent innate immune responses and can be used in the development of novel vaccine adjuvants. However, access to TLRs can be challenging as exemplified by TLR 7, which is located intracellularly in endosomal compartments. To increase recognition and subsequent stimulatory effects of TLR 7, imiquimod was encapsulated in acetalated dextran (Ac-DEX) microparticles. Ac-DEX, a water-insoluble and biocompatible polymer, is relatively stable at pH 7.4, but degrades rapidly under acidic conditions, such as those found in lysosomal vesicles. To determine the immunostimulatory capacity of encapsulated imiquimod, we compared the efficacy of free versus encapsulated imiquimod in activating RAW 264.7 macrophages, MH-S macrophages, and bone marrow derived dendritic cells. Encapsulated imiquimod significantly increased IL-1 beta, IL-6, and TNF-alpha cytokine expression in macrophages relative to the free drug. Furthermore, significant increases were observed in classic macrophage activation markers (iNOS, PD1-L1, and NO) after treatment with encapsulated imiquimod over the free drug. Also, bone marrow derived dendritic cells produced significantly higher levels of IL-1 beta, IL-6, IL-12p70, and MIP-1 alpha as compared to their counterparts receiving free imiquimod. These results suggest that encapsulation of TLR ligands within Ac-DEX microparticles results in increased immunostimulation and potentially better protection from disease when used in conjunction with vaccine formulations.

Indexed as

Adjuvants, ImmunologicAminoquinolinesAnimalsCell LineCells, CulturedDendritic CellsDextransImiquimodInterleukin-12Interleukin-1betaInterleukin-6Macrophage ActivationMiceMicroscopy, Electron, ScanningNanoparticlesPolymerase Chain ReactionAdjuvants, ImmunologicAminoquinolinesDextransImiquimodInterleukin-12Interleukin-1betaInterleukin-6

Identifiers

PMID20230025
PMCPMC2882515
OpenAlexW2009069733

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.