Evidence map›Paper›PMID 38866196›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2024

Immunostimulatory nucleic acid nanoparticles (NANPs) augment protective osteoblast and osteoclast type I interferon responses to Staphylococcus aureus.

Erin L Mills, Yelixza I Avila, Damian Beasock, Yasmine Radwan, Samantha R Suptela, Ian Marriott, Kirill A Afonin, M Brittany Johnson

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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.

Erin L MillsDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: edavi138@charlotte.edu.
Yelixza I AvilaDepartment of Chemistry, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: yavila@charlotte.edu.
Damian BeasockDepartment of Chemistry, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223.
Yasmine RadwanDepartment of Chemistry, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: yradwan@uncc.edu.
Samantha R SuptelaDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: srfurr1@charlotte.edu.
Ian MarriottDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: imarriot@charlotte.edu.
Kirill A AfoninDepartment of Chemistry, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: kafonin@charlotte.edu.
M Brittany JohnsonDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, USA, 28223. Electronic address: mjohn398@charlotte.edu.

Funding

Substance P exacerbation of staphylococcal bone damageR01AI170012 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI Morgan Brittany Johnson, Ian Marriott · 2022 to 2026
$1.9M
SMART NANPs: new molecular platform for communication with human immune system and modulation of therapeutic responsesR35GM139587 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI AFONIN, KIRILL A · 2021 to 2025
$1.8M
Type I interferon responses of bone cells to Staphylococcus aureus: A pilot studyR03AI176300 · NIAID · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI MARRIOTT, IAN · 2024 to 2025
$143k
NIAID NIH HHS R01 AI170012NIAID NIH HHS R03 AI176300NIGMS NIH HHS R35 GM139587
6 · The paper itself

Abstract

Recalcitrant staphylococcal osteomyelitis may be due, in part, to the ability of Staphylococcus aureus to invade bone cells. However, osteoclasts and osteoblasts are now recognized to shape host responses to bacterial infection and we have recently described their ability to produce IFN-β following S. aureus infection and limit intracellular bacterial survival/propagation. Here, we have investigated the ability of novel, rationally designed, nucleic acid nanoparticles (NANPs) to induce the production of immune mediators, including IFN-β, following introduction into bone cells. We demonstrate the successful delivery of representative NANPs into osteoblasts and osteoclasts via endosomal trafficking when complexed with lipid-based carriers. Their delivery was found to differentially induce immune responses according to their composition and architecture via discrete cytosolic pattern recognition receptors. Finally, the utility of this nanoparticle technology was supported by the demonstration that immunostimulatory NANPs augment IFN-β production by S. aureus infected bone cells and reduce intracellular bacterial burden.

Indexed as

NanoparticlesNucleic AcidsOsteoblastsOsteoclastsStaphylococcal InfectionsStaphylococcus aureusAdjuvants, ImmunologicAnimalsHumansInterferon-betaInterferon Type IMiceAdjuvants, ImmunologicInterferon-betaInterferon Type INucleic AcidsCytosolic nucleic acid sensorsNucleic acid nanoparticles (NANPs)OsteoblastsOsteoclastsStaphylococcus aureusType I interferons

Identifiers

PMID38866196
PMCPMC11297679

What Socratic holds

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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 Socratic graph.