Evidence map›Paper›PMID 28703489›Full record

ArticleAdvanced healthcare materials2017

Timed Delivery of Therapy Enhances Functional Muscle Regeneration.

Christine A Cezar, Praveen Arany, Sarah A Vermillion, Bo Ri Seo, Herman H Vandenburgh, David J Mooney

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Cell therapy to improve regeneration of skeletal muscle injuries.Journal of cachexia, sarcopenia and muscle · 2019
    Review
  4. Article
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 at 3 institutions in 1 country.

Christine A CezarHarvard School of Engineering and Applied Sciences, 29 Oxford Street, Cambridge, MA, 02138, USA.
Praveen AranyDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, 3435 Main Street, Buffalo, NY, 14260, USA.
Sarah A VermillionHarvard School of Engineering and Applied Sciences, 29 Oxford Street, Cambridge, MA, 02138, USA.
Bo Ri SeoHarvard School of Engineering and Applied Sciences, 29 Oxford Street, Cambridge, MA, 02138, USA.
Herman H VandenburghDepartment of Pathology and Lab Medicine, Brown University, Providence, RI, 02912, USA.
David J MooneyHarvard School of Engineering and Applied Sciences, 29 Oxford Street, Cambridge, MA, 02138, USA.
Harvard University · USBrown University · USUniversity at Buffalo, State University of New York · US

Funding

ENGINEERING SKELETAL MUSCLE WITH BIODEGRADABLE HYDROGELSR01DE013349 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOONEY, DAVID J · 2000 to 2022
$9.3M
NIDCR NIH HHS R01 DE013349
6 · The paper itself

Abstract

Cell transplantation is a promising therapeutic strategy for the treatment of traumatic muscle injury in humans. Previous investigations have typically focused on the identification of potent cell and growth factor treatments and optimization of spatial control over delivery. However, the optimal time point for cell transplantation remains unclear. Here, this study reports how myoblast and morphogen delivery timed to coincide with specific phases of the inflammatory response affects donor cell engraftment and the functional repair of severely injured muscle. Delivery of a biomaterial-based therapy timed with the peak of injury-induced inflammation leads to potent early and long-term regenerative benefits. Diminished inflammation and fibrosis, enhanced angiogenesis, and increased cell engraftment are seen during the acute stage following optimally timed treatment. Over the long term, treatment during peak inflammation leads to enhanced functional regeneration, as indicated by reduced chronic inflammation and fibrosis along with increased tissue perfusion and muscle contractile force. Treatments initiated immediately after injury or after inflammation had largely resolved provided more limited benefits. These results demonstrate the importance of appropriately timing the delivery of biologic therapy in the context of muscle regeneration. Biomaterial-based timed delivery can likely be applied to other tissues and is of potential wide utility in regenerative medicine.

Indexed as

AnimalsDelayed-Action PreparationsIntercellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLMuscle DevelopmentMuscle Fibers, SkeletalMuscular DiseasesRegenerationTime FactorsTissue ScaffoldsTreatment OutcomeDelayed-Action PreparationsIntercellular Signaling Peptides and Proteinscell therapycontrolled deliveryferrogel scaffoldsinflammation kineticsmagnetic biomaterials

Identifiers

PMID28703489
PMCPMC5641972
OpenAlexW2735070612

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.