Evidence map›Paper›PMID 28435136›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2017

Chitosan enhances nanoparticle delivery from the reproductive tract to target draining lymphoid organs.

Jaehyung Park, Renuka Ramanathan, Linhchi Pham, Kim A Woodrow

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Advances in Chitosan-Based Nanoparticles for Drug Delivery.International journal of molecular sciences · 2021
    Review
  4. Review
  5. Flt3-L enhances trans-epithelial migration and antigen presentation of dendritic cells adoptively transferred to genital mucosa.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  6. Article
  7. 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

4 authors at 1 institution in 1 country.

Jaehyung ParkDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Renuka RamanathanDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Linhchi PhamDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Kim A WoodrowDepartment of Bioengineering, University of Washington, Seattle, WA, USA. Electronic address: woodrow@u.washington.edu.
University of Washington · US

Funding

Nanomaterials for engineering protection in the genital mucosaDP2HD075703 · NICHD · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2012 to 2012
$2.3M
Nanoparticle microbicides for delivery of combination antiretroviral drugsR33AI094412 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2013 to 2015
$1.6M
Biomaterials that Promote Infection ImmunityR56AI074661 · NIAID · UNIVERSITY OF WASHINGTON · PI BRYERS, JAMES D. · 2015 to 2015
$400k
Nanoparticle microbicides for delivery of combination antiretroviral drugsR21AI094412 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODROW, KIM A. · 2011 to 2012
$394k
NIAID NIH HHS R21 AI094412NIAID NIH HHS R33 AI094412NIAID NIH HHS R56 AI074661NICHD NIH HHS DP2 HD075703
6 · The paper itself

Abstract

To prime adaptive immune responses from the female reproductive tract (FRT), particulate antigens must be transported to draining lymph nodes (dLNs) since there are no local organized lymphoid structures equivalent to those found in the respiratory or gastrointestinal tracts. However, little is known about how to safely and effectively navigate successive barriers to transport such as crossing the epithelium and gaining access to migratory cells and lymphatic drainage that provide entry into dLNs. Here, we demonstrate that intravaginal pre-treatment with chitosan significantly facilitates translocation of nanoparticles (NPs) across the multilayered vaginal epithelium to target dLNs. In addition, chitosan pre-treatment was found to enhance NP associations with immunogenic antigen presenting cells in the vaginal submucosa. These observations indicate that chitosan may have great potential as an adjuvant for both local and systemic protective immunity against viral infections in the FRT.

Indexed as

Adjuvants, ImmunologicDrug Delivery SystemsAnimalsAntigensChitosanDendritic CellsFemaleLymphoid TissueMice, Inbred C57BLNanoparticlesVaginaAdjuvants, ImmunologicAntigensChitosanChitosanDraining lymph nodeMucosal deliveryNanoparticleReproductive tract

Identifiers

PMID28435136
PMCPMC5544568
OpenAlexW2606945473

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.