Literature DB >> 33633730

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

E Eduardo Sanchez-Castro1, Cecilia Pajuelo-Reyes2, Rebeca Tejedo3, Bárbara Soria-Juan4,5, Rafael Tapia-Limonchi2, Etelvina Andreu6,7, Ana B Hitos8,9, Franz Martin4,8,9, Gladys M Cahuana4,8, Clara Guerra-Duarte10, Thamyres C Silva de Assis11, Francisco J Bedoya4,8,9, Bernat Soria4,6,9,12, Carlos Chávez-Olórtegui11, Juan R Tejedo2,4,8,9.   

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.
Copyright © 2021 Sanchez-Castro, Pajuelo-Reyes, Tejedo, Soria-Juan, Tapia-Limonchi, Andreu, Hitos, Martin, Cahuana, Guerra-Duarte, de Assis, Bedoya, Soria, Chávez-Olórtegui and Tejedo.

Entities:  

Keywords:  advanced therapy medicinal products; envenoming; mesenchymal stromal cells; muscle regeneration; snakebite

Year:  2021        PMID: 33633730      PMCID: PMC7902043          DOI: 10.3389/fimmu.2020.609961

Source DB:  PubMed          Journal:  Front Immunol        ISSN: 1664-3224            Impact factor:   7.561


  118 in total

1.  Angiographic demonstration of neoangiogenesis after intra-arterial infusion of autologous bone marrow mononuclear cells in diabetic patients with critical limb ischemia.

Authors:  Rafael Ruiz-Salmeron; Antonio de la Cuesta-Diaz; Manuel Constantino-Bermejo; Immaculada Pérez-Camacho; Francisco Marcos-Sánchez; Abdelkrim Hmadcha; Bernat Soria
Journal:  Cell Transplant       Date:  2011       Impact factor: 4.064

Review 2.  Venomics: integrative venom proteomics and beyond.

Authors:  Juan J Calvete
Journal:  Biochem J       Date:  2017-02-20       Impact factor: 3.857

Review 3.  Mechanisms of mesenchymal stromal cell immunomodulation.

Authors:  Karen English
Journal:  Immunol Cell Biol       Date:  2012-10-23       Impact factor: 5.126

Review 4.  An overview of international regulatory frameworks for mesenchymal stromal cell-based medicinal products: From laboratory to patient.

Authors:  Javier López-Beas; Juan A Guadix; Beatriz Clares; Jose L Soriano-Ruiz; José L Zugaza; Patricia Gálvez-Martín
Journal:  Med Res Rev       Date:  2020-02-04       Impact factor: 12.944

Review 5.  Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases.

Authors:  Teresa Escalante; Alexandra Rucavado; Jay W Fox; José María Gutiérrez
Journal:  J Proteomics       Date:  2011-04-06       Impact factor: 4.044

Review 6.  Snakebite envenoming.

Authors:  José María Gutiérrez; Juan J Calvete; Abdulrazaq G Habib; Robert A Harrison; David J Williams; David A Warrell
Journal:  Nat Rev Dis Primers       Date:  2017-09-14       Impact factor: 52.329

7.  Inflammation induced by Bothrops asper venom: release of proinflammatory cytokines and eicosanoids, and role of adhesion molecules in leukocyte infiltration.

Authors:  Stella Regina Zamuner; Juliana Pavan Zuliani; Cristina Maria Fernandes; José Maria Gutiérrez; Catarina de Fátima Pereira Teixeira
Journal:  Toxicon       Date:  2005-09-29       Impact factor: 3.033

Review 8.  Regeneration of mammalian skeletal muscle. Basic mechanisms and clinical implications.

Authors:  Stefano Ciciliot; Stefano Schiaffino
Journal:  Curr Pharm Des       Date:  2010       Impact factor: 3.116

9.  Entry of muscle satellite cells into the cell cycle requires sphingolipid signaling.

Authors:  Yosuke Nagata; Terence A Partridge; Ryoichi Matsuda; Peter S Zammit
Journal:  J Cell Biol       Date:  2006-07-17       Impact factor: 10.539

10.  The microRNA regulatory landscape of MSC-derived exosomes: a systems view.

Authors:  Scott W Ferguson; Jinli Wang; Christine J Lee; Maixian Liu; Sriram Neelamegham; John M Canty; Juliane Nguyen
Journal:  Sci Rep       Date:  2018-01-23       Impact factor: 4.379

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  1 in total

Review 1.  The Search for Natural and Synthetic Inhibitors That Would Complement Antivenoms as Therapeutics for Snakebite Envenoming.

Authors:  José María Gutiérrez; Laura-Oana Albulescu; Rachel H Clare; Nicholas R Casewell; Tarek Mohamed Abd El-Aziz; Teresa Escalante; Alexandra Rucavado
Journal:  Toxins (Basel)       Date:  2021-06-29       Impact factor: 4.546

  1 in total

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