Evidence map›Paper›PMID 34460818›Full record

ArticlePloS one2021

Gold nanorods enhance different immune cells and allow for efficient targeting of CD4+ Foxp3+ Tregulatory cells.

Ingrid Safina, Zeid A Nima Al Sudani, Ahmed Hashoosh, Emilie Darrigues, Fumiya Watanabe, Alexandru S Biris, Ruud P M Dings, Kieng Bao Vang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 2 institutions in 1 country.

Ingrid SafinaCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Zeid A Nima Al SudaniCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Ahmed HashooshCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Emilie DarriguesCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Fumiya WatanabeCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Alexandru S BirisCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Ruud P M DingsDepartment of Radiation Oncology, Phillips Classic Laser and Nanomedicine Laboratories, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
Kieng Bao VangCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.ORCID 0000-0002-2892-1114
University of Arkansas at Little Rock · USUniversity of Arkansas for Medical Sciences · US

Funding

Understanding Hesitant AdoptersP20GM103429 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Lawrence E Cornett, JERRY WARE · 2012 to 2026
$60.9M
Study of the Cell-specific Inflammasome Responses During Defense Against Gram-negative BacteriaP20GM103625 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI SMELTZER, MARK S · 2012 to 2021
$21.5M
NIGMS NIH HHS P20 GM103429NIGMS NIH HHS P20 GM103625
6 · The paper itself

Abstract

Gold nanoparticles (AuNPs) hold great promise in nanomedicine, yet their successful clinical translation has not been realized. Some challenges include effective AuNP targeting and delivery to improve modulation of immune cells of interest while limiting potential adverse effects. In order to overcome these challenges, we must fully understand how AuNPs impact different immune cell subsets, particularly within the dendritic cell and T cell compartments. Herein, we show that polyethylene glycol coated (PEG) gold nanorods (AuNRs) and PEG AuNRs covered with a thin layer of silver (AuNR/Ag) may enhance the immune response towards immune suppression or activation. We also studied the ability to enhance CD4+ Foxp3+ Tregs in vitro using AuNRs functionalized with interleukin 2 (IL2), a cytokine that is important in Treg development and homeostasis. Our results indicate that AuNRs enhance different immune cells and that NP composition matters in immune targeting. This knowledge will help us understand how to better design AuNRs to target and enhance the immune system.

Indexed as

AnimalsCD4-Positive T-LymphocytesDendritic CellsForkhead Transcription FactorsGoldImmune SystemImmunityInterleukin-2Metal NanoparticlesMiceMice, Inbred C57BLNanotubesPolyethylene GlycolsSilverForkhead Transcription FactorsFoxp3 protein, mouseGoldInterleukin-2Polyethylene GlycolsSilver

Identifiers

PMID34460818
PMCPMC8404976
OpenAlexW3198855627

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.