Evidence map›Paper›PMID 33633730›Full record

ReviewFrontiers in immunology2020

Mesenchymal Stromal Cell-Based Therapies as Promising Treatments for Muscle Regeneration After Snakebite Envenoming.

E Eduardo Sanchez-Castro, Cecilia Pajuelo-Reyes, Rebeca Tejedo, Bárbara Soria-Juan, Rafael Tapia-Limonchi, Etelvina Andreu, Ana B Hitos, Franz Martin, Gladys M Cahuana, Clara Guerra-Duarte and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Protective effects of mesenchymal stromal cell-derived secretome on dermonecrosis induced in rabbits byThe journal of venomous animals and toxins including tropical diseases · 2024
    Article
  9. Article
  10. 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

15 authors at 10 institutions in 3 countries.

E Eduardo Sanchez-CastroFaculty of Biological Sciences, Universidad Nacional Mayor de San Marcos, Lima, Peru.
Cecilia Pajuelo-ReyesInstitute of Tropical Diseases, Universidad Nacional Toribio Rodríguez de Mendoza de Amazonas, Chachapoyas, Peru.
Rebeca TejedoFaculty of Medicine, Universidad Privada San Juan Bautista, Lima, Peru.
Bárbara Soria-JuanDepartment of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Rafael Tapia-LimonchiInstitute of Tropical Diseases, Universidad Nacional Toribio Rodríguez de Mendoza de Amazonas, Chachapoyas, Peru.
Etelvina AndreuISABIAL-Hospital General y Universitario de Alicante, Alicante, Spain.
Ana B HitosDepartment of Cell Regeneration and Advanced Therapies, Andalusian Center of Molecular Biology and Regenerative Medicine-CABIMER, University of Pablo de Olavide-University of Sevilla-CSIC, Seville, Spain.
Franz MartinDepartment of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Gladys M CahuanaDepartment of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Clara Guerra-DuarteCenter of Research and Development, Fundação Ezequiel Dias, Belo Horizonte, Brazil.
Thamyres C Silva de AssisDepartament of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Francisco J BedoyaDepartment of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Bernat SoriaDepartment of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Carlos Chávez-OlórteguiDepartament of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Juan R TejedoInstitute of Tropical Diseases, Universidad Nacional Toribio Rodríguez de Mendoza de Amazonas, Chachapoyas, Peru.
Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESNational University Toribio Rodríguez de Mendoza · PEUniversidade Federal de Minas Gerais · BRUniversidad Pablo de Olavide · ESCentro Andaluz de Biología Molecular y Medicina Regenerativa · ESEzequiel Dias Foundation · BRHospital General Universitario de Alicante Doctor Balmis · ESInstituto de Salud Carlos III · ESNational University of San Marcos · PEUniversidad Privada San Juan Bautista · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Snakebite envenoming is a global neglected disease with an incidence of up to 2.7 million new cases every year. Although antivenoms are so-far the most effective treatment to reverse the acute systemic effects induced by snakebite envenoming, they have a limited therapeutic potential, being unable to completely neutralize the local venom effects. Local damage, such as dermonecrosis and myonecrosis, can lead to permanent sequelae with physical, social, and psychological implications. The strong inflammatory process induced by snake venoms is associated with poor tissue regeneration, in particular the lack of or reduced skeletal muscle regeneration. Mesenchymal stromal cells (MSCs)-based therapies have shown both anti-inflammatory and pro-regenerative properties. We postulate that using allogeneic MSCs or their cell-free products can induce skeletal muscle regeneration in snakebite victims, improving all the three steps of the skeletal muscle regeneration process, mainly by anti-inflammatory activity, paracrine effects, neovascularization induction, and inhibition of tissue damage, instrumental for microenvironment remodeling and regeneration. Since snakebite envenoming occurs mainly in areas with poor healthcare, we enlist the principles and potential of MSCs-based therapies and discuss regulatory issues, good manufacturing practices, transportation, storage, and related-procedures that could allow the administration of these therapies, looking forward to a safe and cost-effective treatment for a so far unsolved and neglected health problem.

Indexed as

Mesenchymal Stem Cell TransplantationMuscle DevelopmentRegenerationAnimalsHumansInflammation MediatorsMesenchymal Stem CellsMuscle, SkeletalNecrosisPhenotypeSignal TransductionSnake BitesTreatment OutcomeInflammation Mediatorsadvanced therapy medicinal productsenvenomingmesenchymal stromal cellsmuscle regenerationsnakebite

Identifiers

PMID33633730
PMCPMC7902043
OpenAlexW3126238272

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.