Evidence map›Paper›PMID 38280914›Full record

ArticleNPJ Regenerative medicine2024

Matrix-bound nanovesicle-associated IL-33 supports functional recovery after skeletal muscle injury by initiating a pro-regenerative macrophage phenotypic transition.

J G Bartolacci, M N Behun, J P Warunek, T Li, A Sahu, G K Dwyer, A Lucas, J Rong, F Ambrosio, H R Turnquist and 1 more

Open access · goldAbstract read
In one paragraph

Article in NPJ Regenerative medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  12. Macrophages and the Extracellular Matrix.Results and problems in cell differentiation · 2024
    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

11 authors at 3 institutions in 1 country.

J G Bartolacci *Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
M N Behun *Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
J P Warunek *Departments of Surgery and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.ORCID http://orcid.org/0000-0002-5430-9834
T LiDepartments of Surgery and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
A SahuDepartment of Physical Medicine and Rehabilitation Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
G K DwyerDepartments of Surgery and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
A LucasDepartments of Surgery and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
J RongMcGowan Institute for Regenerative Medicine, Pittsburgh, USA.
F AmbrosioDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
H R TurnquistDepartments of Surgery and Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA. turnquisthr@upmc.edu.
S F BadylakDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA. badylaks@upmc.edu.ORCID http://orcid.org/0000-0003-3555-0689
University of Pittsburgh · USUniversity of Pittsburgh Medical Center · USMcGowan Institute for Regenerative Medicine · US

Funding

Training in Cellular & Molecular Mechanisms of Tumor RejectionT32CA082084 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Robert J Binder, Dario AA Vignali · 1999 to 2026
$9.2M
Immunoregulatory Mechanisms of IL-33 in Heart TransplantationR01HL122489 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Heth R Turnquist · 2015 to 2026
$4.9M
Mechanisms of functional skeletal muscle repair: critical role of matrix associated IL-33R01AR073527 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BADYLAK, STEPHEN F., TURNQUIST, HETH R · 2018 to 2022
$2.6M
Special BD LSRFortessaTMS10OD011925 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BORGHESI, LISA · 2012 to 2012
$383k
Defining the IL-33 signaling networks in allogeneic T cells that mediate graft vs. host diseaseF30AI147437 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DWYER, GAELEN · 2020 to 2022
$154k
NCI NIH HHS T32 CA082084NHLBI NIH HHS R01 HL122489NIAID NIH HHS F30 AI147437NIAMS NIH HHS R01 AR073527NIH HHS S10 OD011925
6 · The paper itself

Abstract

Injuries to skeletal muscle are among the most common injuries in civilian and military populations, accounting for nearly 60% of extremity injuries. The standard of care for severe extremity injury has been focused upon limb salvage procedures and the utilization of tissue grafts or orthotics in conjunction with rehabilitation to avoid amputation. Nonetheless, many patients have persistent strength and functional deficits that permanently impact their quality of life. Preclinical and clinical studies have shown that partial restoration of functional skeletal muscle tissue following injury can be achieved by the implantation of a biologic scaffold composed of extracellular matrix (ECM). These favorable outcomes are mediated, at least in part, through local immunomodulation. The mechanisms underlying this immunomodulatory effect, however, are poorly understood. The present study investigates a potential mechanistic driver of the immunomodulatory effects; specifically, the effect of selected ECM components upon inflammation resolution and repair. Results show that the host response to skeletal muscle injury is profoundly altered and functional recovery decreased in il33

Identifiers

PMID38280914
PMCPMC10821913
OpenAlexW4391282729

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.