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About:
Shattering barriers toward clinically meaningful MSC therapies
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An Entity of Type :
schema:ScholarlyArticle
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wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Shattering barriers toward clinically meaningful MSC therapies
Creator
Levy, Oren
Abdi, Reza
Alhasan, Ali
Almalik, Abdulaziz
Alturki, Meshael
Bhere, Deepak
De Biasio, Michael
Fallatah, Mohanad
Heinelt, Martina
Karp, Jeffrey
Kuai, Rui
Milton, Yuka
Nissar, Nabeel
Reeve, Brock
Shah, Khalid
Siren, Erika
topic
covid:687959aa46ad99efd81baefd9d27149a9cc86d92#this
Source
Medline; PMC
abstract
More than 1050 clinical trials are registered at FDA.gov that explore multipotent mesenchymal stromal cells (MSCs) for nearly every clinical application imaginable, including neurodegenerative and cardiac disorders, perianal fistulas, graft-versus-host disease, COVID-19, and cancer. Several companies have or are in the process of commercializing MSC-based therapies. However, most of the clinical-stage MSC therapies have been unable to meet primary efficacy end points. The innate therapeutic functions of MSCs administered to humans are not as robust as demonstrated in preclinical studies, and in general, the translation of cell-based therapy is impaired by a myriad of steps that introduce heterogeneity. In this review, we discuss the major clinical challenges with MSC therapies, the details of these challenges, and the potential bioengineering approaches that leverage the unique biology of MSCs to overcome the challenges and achieve more potent and versatile therapies.
has issue date
2020-07-22
(
xsd:dateTime
)
bibo:doi
10.1126/sciadv.aba6884
bibo:pmid
32832666
has license
cc-by-nc
sha1sum (hex)
687959aa46ad99efd81baefd9d27149a9cc86d92
schema:url
https://doi.org/10.1126/sciadv.aba6884
resource representing a document's title
Shattering barriers toward clinically meaningful MSC therapies
has PubMed Central identifier
PMC7439491
has PubMed identifier
32832666
schema:publication
Sci Adv
resource representing a document's body
covid:687959aa46ad99efd81baefd9d27149a9cc86d92#body_text
is
http://vocab.deri.ie/void#inDataset
of
https://covidontheweb.inria.fr:4443/about/id/http/ns.inria.fr/covid19/687959aa46ad99efd81baefd9d27149a9cc86d92
is
schema:about
of
named entity 'Adv.'
named entity 'efficacy'
named entity 'potent'
named entity 'therapies'
named entity 'MSC'
named entity 'COMPANIES'
named entity 'therapies'
named entity 'process'
named entity 'More'
named entity 'potential'
named entity 'MSC'
named entity 'therapy'
named entity 'general'
named entity 'perianal'
named entity 'clinical trials'
named entity 'A L'
named entity 'heterogeneity'
named entity 'clinically meaningful'
named entity 'cardiac disorders'
named entity 'neurodegenerative'
named entity 'clinical-stage'
named entity 'fistulas'
named entity 'demonstrated'
named entity 'bone marrow'
named entity 'intravenously'
named entity 'MSCs'
named entity 'mechanism of action'
named entity 'insulin'
named entity 'double-blind, placebo-controlled'
named entity 'MSCs'
named entity 'stiffness'
named entity 'stemness'
named entity 'subcutaneous'
named entity 'saline'
named entity 'macrophages'
named entity 'animal model'
named entity 'biopsy'
named entity 'positively correlated'
named entity 'MSCs'
named entity 'phase 1/2'
named entity 'MSCs'
named entity 'herpes simplex virus'
named entity 'host immune responses'
named entity 'systemic administration'
named entity 'MSCs'
named entity 'up-regulated'
named entity 'iPSCs'
named entity 'MSCs'
named entity 'rodents'
named entity '36 hours'
named entity 'medicinal product'
named entity 'cytokine secretion'
named entity 'inflammation'
named entity 'clinical studies'
named entity 'glioblastoma'
named entity 'MSCs'
named entity 'route of administration'
named entity 'Quality control'
named entity 'phase 2 study'
named entity 'cancer cells'
named entity 'preclinical studies'
named entity 'drug release'
named entity 'hyaluronic acid'
named entity 'MSCs'
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