Evidence map›Paper›PMID 25068589›Full record

ArticleJournal of biomaterials science. Polymer edition2014

Carbohydrate-functionalized nanovaccines preserve HIV-1 antigen stability and activate antigen presenting cells.

J E Vela Ramirez, R Roychoudhury, H H Habte, M W Cho, N L B Pohl, B Narasimhan

Abstract read
In one paragraph

Article in Journal of biomaterials science. Polymer edition, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Polyanhydride nanoparticles stabilize pancreatic cancer antigen MUC4β.Journal of biomedical materials research. Part A · 2021
    Article
  7. Review
  8. Polymeric Nanoparticle-Based Vaccine Adjuvants and Delivery Vehicles.Current topics in microbiology and immunology · 2021
    Review
  9. Review
  10. Applications of Nanovaccines for Disease Prevention in Cattle.Frontiers in bioengineering and biotechnology · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

6 authors.

J E Vela Ramireza Department of Chemical and Biological Engineering , Iowa State University , Ames , IA 50011 , USA.
R Roychoudhury
H H Habte
M W Cho
N L B Pohl
B Narasimhan

Funding

Vaccine Delivery Platform DevelopmentU19AI091031 · NIAID · IOWA STATE UNIVERSITY · PI CHO, MICHAEL W · 2010 to 2013
$5.1M
NIAID NIH HHS U19 AI-091031NIAID NIH HHS U19 AI091031
6 · The paper itself

Abstract

The functionalization of polymeric nanoparticles with ligands that target specific receptors on immune cells offers the opportunity to tailor adjuvant properties by conferring pathogen mimicking attributes to the particles. Polyanhydride nanoparticles are promising vaccine adjuvants with desirable characteristics such as immunomodulation, sustained antigen release, activation of antigen presenting cells (APCs), and stabilization of protein antigens. These capabilities can be exploited to design nanovaccines against viral pathogens, such as HIV-1, due to the important role of dendritic cells (DCs) and macrophages in viral spread. In this work, an optimized process was developed for carbohydrate functionalization of HIV-1 antigen-loaded polyanhydride nanoparticles. The carbohydrate-functionalized nanoparticles preserved antigenic properties upon release and also enabled sustained antigen release kinetics. Particle internalization was observed to be chemistry-dependent with positively charged nanoparticles being taken up more efficiently by DCs. Up-regulation of the activation makers CD40 and CD206 was demonstrated with carboxymethyl-α-d-mannopyranosyl-(1,2)-d-mannopyranoside functionalized nanoparticles. The secretion of the cytokines IL-6 and TNF-α was shown to be chemistry-dependent upon stimulation with carbohydrate-functionalized nanoparticles. These results offer important new insights upon the interactions between carbohydrate-functionalized nanoparticles and APCs and provide foundational information for the rational design of targeted nanovaccines against HIV-1.

Indexed as

Adjuvants, ImmunologicAIDS VaccinesAnimalsCarbohydratesCD40 AntigensCells, CulturedDendritic CellsHIV-1HIV Envelope Protein gp41Interleukin-6Lectins, C-TypeMannose-Binding LectinsMannose ReceptorMice, Inbred C57BLNanoparticlesPolyanhydridesAdjuvants, ImmunologicAIDS VaccinesCarbohydratesCD40 AntigensHIV Envelope Protein gp41Interleukin-6interleukin-6, mouseLectins, C-TypeMannose-Binding LectinsMannose ReceptorPolyanhydridesReceptors, Cell SurfaceTumor Necrosis Factor-alphaVaccines, Syntheticcarbohydratesdendritic cellsHIV antigennanoparticlesnanovaccinespolyanhydridestargeting

Identifiers

PMID25068589
PMCPMC4465578

What OpenQuestion holds

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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.