Evidence map›Paper›PMID 35229011›Full record

ArticleRegenerative therapy2022

Repair of ovine peripheral nerve injuries with xenogeneic human acellular sciatic nerves prerecellularized with allogeneic Schwann-like cells-an innovative and promising approach.

Florencia-E Pedroza-Montoya, Yadira-A Tamez-Mata, Mario Simental-Mendía, Adolfo Soto-Domínguez, Mauricio-M García-Pérez, Salvador Said-Fernández, Roberto Montes-de-Oca-Luna, José-R González-Flores, Herminia-G Martínez-Rodríguez, Félix Vilchez-Cavazos

Open access · goldAbstract read
In one paragraph

Article in Regenerative therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Florencia-E Pedroza-MontoyaAutonomous University of Nuevo Leon (UANL), Medicine School, Department of Biochemistry and Molecular Medicine, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Yadira-A Tamez-MataUANL, Medicine School and University Hospital "Dr. José Eleuterio González", Orthopedics and Traumatology Service, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Mario Simental-MendíaUANL, Medicine School and University Hospital "Dr. José Eleuterio González", Orthopedics and Traumatology Service, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Adolfo Soto-DomínguezUANL, Medicine School, Department of Histology, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Mauricio-M García-PérezUANL, Medicine School and University Hospital "Dr. José. Eleuterio González" Service of Plastic Surgery, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Salvador Said-FernándezAutonomous University of Nuevo Leon (UANL), Medicine School, Department of Biochemistry and Molecular Medicine, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Roberto Montes-de-Oca-LunaUANL, Medicine School, Department of Histology, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
José-R González-FloresUANL, Medicine School and University Hospital "Dr. José. Eleuterio González" Service of Plastic Surgery, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Herminia-G Martínez-RodríguezAutonomous University of Nuevo Leon (UANL), Medicine School, Department of Biochemistry and Molecular Medicine, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Félix Vilchez-CavazosUANL, Medicine School and University Hospital "Dr. José Eleuterio González", Orthopedics and Traumatology Service, Av. Madero and Dr. Eduardo Aguirre Pequeño S/N Col. Mitras Centro, Monterrey, Nuevo Leon C.P 64460, Mexico.
Hospital Universitario Dr José Eleuterio Gonzalez · MXUniversidad Autónoma de Nuevo León · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe iatrogenic effects of repairing peripheral nerve injuries (PNIs) with autografts (AGTs) encouraged the present study to involve a new approach consisting of grafting xenogeneic prerecellularized allogeneic cells instead of AGTs.

methodsWe compared sheep's AGT regenerative and functional capacity with decellularized human nerves prerecellularized with allogeneic Schwann-like cell xenografts (onwards called xenografts). Mesenchymal stem cells were isolated from ovine adipose tissue and induced in vitro to differentiate into Schwann-like cells (SLCs). Xenografts were grafted in ovine sciatic nerves. Left sciatic nerves (20 mm) were excised from 10 sheep. Then, five sheep were grafted with 20 mm xenografts, and five were reimplanted with their nerve segment rotated 180° (AGT).

resultsAll sheep treated with xenografts or AGT progressively recovered the strength, movement, and coordination of their intervened limb, which was still partial when the study was finished at sixth month postsurgery. At this time, numerous intrafascicular axons were observed in the distal and proximal graft extremes of both xenografts or AGTs, and submaximal nerve electrical conduction was observed. The xenografts and AGT-affected muscles appeared partially stunted.

conclusionsXenografts and AGT were equally efficacious in starting PNI repair and justified further studies using longer observation times. The hallmarks from this study are that human xenogeneic acellular scaffolds were recellularized with allogenic SCL and were not rejected by the nonhuman receptors but were also as functional as AGT within a relatively short time postsurgery. Thus, this innovative approach promises to be more practical and accessible than AGT or allogenic allografts and safer than AGT for PNI repair.

Indexed as

Acellular graftAutograftPeripheral nerve injurySchwann-like cellsSciatic nerveXenograft

Identifiers

PMID35229011
PMCPMC8850753
OpenAlexW4211111808

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.