Evidence map›Paper›PMID 27824330›Full record

ArticleGene therapy2017

Effect of sustained PDGF nonviral gene delivery on repair of tooth-supporting bone defects.

A B Plonka, B Khorsand, N Yu, J V Sugai, A K Salem, W V Giannobile, S Elangovan

Open access · bronzeAbstract read
In one paragraph

Article in Gene therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 46 citations in OpenAlex.

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  5. Comparison ofBiofabrication · 2022
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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

7 authors at 2 institutions in 1 country.

A B PlonkaDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry. Ann Arbor, MI, USA.
B KhorsandDivision of Pharmaceutics and Translational Therapeutics, The University of Iowa College of Pharmacy, Iowa City, IA, USA.
N YuDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry. Ann Arbor, MI, USA.
J V SugaiDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry. Ann Arbor, MI, USA.
A K SalemDivision of Pharmaceutics and Translational Therapeutics, The University of Iowa College of Pharmacy, Iowa City, IA, USA.
W V GiannobileDepartment of Periodontics and Oral Medicine, University of Michigan School of Dentistry. Ann Arbor, MI, USA.
S ElangovanDepartment of Periodontics, The University of Iowa College of Dentistry and Dental Clinics, Iowa City, IA, USA.
University of Michigan–Ann Arbor · USUniversity of Iowa · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
GENE THERAPY FOR RECONSTRUCTING PERIODONTAL TISSUESR01DE013397 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GIANNOBILE, WILLIAM V · 2000 to 2014
$4.0M
A Novel RNA Based Biomaterial for Bone RegenerationR21DE024206 · NIDCR · UNIVERSITY OF IOWA · PI ELANGOVAN, SATHEESH · 2015 to 2016
$406k
NIDCR NIH HHS R01 DE013397NIDCR NIH HHS R21 DE024206NIEHS NIH HHS P30 ES005605
6 · The paper itself

Abstract

Recombinant human platelet-derived growth factor-BB (rhPDGF-BB) promotes soft tissue and bone healing, and is Food and Drug Administration-approved for treatment of diabetic ulcers and periodontal defects. The short half-life of topical rhPDGF-BB protein application necessitates bolus, high-dose delivery. Gene therapy enables sustained local growth factor production. A novel gene activated matrix delivering polyplexes of polyethylenimine (PEI)-plasmid DNA encoding PDGF was evaluated for promotion of periodontal wound repair in vivo. PEI-pPDGF-B polyplexes were tested in human periodontal ligament fibroblasts and human gingival fibroblasts for cell viability and transfection efficiency. Collagen scaffolds containing PEI-pPDGF-B polyplexes at two doses, rhPDGF-BB, PEI vector or collagen alone were randomly delivered to experimentally induced tooth-supporting periodontal defects in a rodent model. Mandibulae were collected at 21 days for histologic observation and histomorphometry. PEI-pPDGF-B polyplexes were biocompatible to cells tested and enzyme-linked immunosorbent assay confirmed the functionality of transfection. Significantly greater osteogenesis was observed for collagen alone and rhPDGF-BB versus the PEI-containing groups. Defects treated with sustained PDGF gene delivery demonstrated delayed healing coupled with sustained inflammatory cell infiltrates lateral to the osseous defects. Continuous PDGF-BB production by nonviral gene therapy could have delayed bone healing. This nonviral gene delivery system in this model appeared to prolong inflammatory response, slowing alveolar bone regeneration in vivo.

Indexed as

Bone RegenerationOsteogenesisAnimalsBiocompatible MaterialsFibroblastsGene Transfer TechniquesHumansPeriodontal DiseasesPlatelet-Derived Growth FactorPolyethyleneimineRatsRats, Sprague-DawleyRecombinant ProteinsBiocompatible MaterialsPlatelet-Derived Growth FactorPolyethyleneimineRecombinant Proteins

Identifiers

PMID27824330
PMCPMC5269540
OpenAlexW2549244944

What OpenQuestion 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 OpenQuestion graph.