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About:
Genetically Modified Mesenchymal Stromal/Stem Cells: Application in Critical Illness
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schema:ScholarlyArticle
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wasabi.inria.fr
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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
Genetically Modified Mesenchymal Stromal/Stem Cells: Application in Critical Illness
Creator
To,
Dos Santos, Claudia
Ka, Li
Paula, Ana
Mei, Shirley
Stewart, Duncan
Tsoporis, James
Varkouhi, Amir
Claudia, Santos
Dos, Claudia
Dossantos@unityhealth,
Monteiro, Teixeira
Source
Medline; PMC
abstract
Critical illnesses including sepsis, acute respiratory distress syndromes, ischemic cardiovascular disorders and acute organ injuries are associated with high mortality, morbidity as well as significant health care system expenses. While these diverse conditions require different specific therapeutic approaches, mesenchymal stem/stromal cell (MSCs) are multipotent cells capable of self-renewal, tri-lineage differentiation with a broad range regenerative and immunomodulatory activities, making them attractive for the treatment of critical illness. The therapeutic effects of MSCs have been extensively investigated in several pre-clinical models of critical illness as well as in phase I and II clinical cell therapy trials with mixed results. Whilst these studies have demonstrated the therapeutic potential for MSC therapy in critical illness, optimization for clinical use is an ongoing challenge. MSCs can be readily genetically modified by application of different techniques and tools leading to overexpress or inhibit genes related to their immunomodulatory or regenerative functions. Here we will review recent approaches designed to enhance the therapeutic potential of MSCs with an emphasis on the technology used to generate genetically modified cells, target genes, target diseases and the implication of genetically modified MSCs in cell therapy for critical illness.
has issue date
2020-07-15
(
xsd:dateTime
)
bibo:doi
10.1007/s12015-020-10000-1
bibo:pmid
32671645
has license
no-cc
sha1sum (hex)
7c712b760940ec3143bd3145c855f0056020763e
schema:url
https://doi.org/10.1007/s12015-020-10000-1
resource representing a document's title
Genetically Modified Mesenchymal Stromal/Stem Cells: Application in Critical Illness
has PubMed Central identifier
PMC7363458
has PubMed identifier
32671645
schema:publication
Stem Cell Rev Rep
resource representing a document's body
covid:7c712b760940ec3143bd3145c855f0056020763e#body_text
is
schema:about
of
named entity 'MSC'
named entity 'conditions'
named entity 'range'
named entity 'genes'
named entity 'investigated'
named entity 'respiratory distress'
named entity 'critical illness'
named entity 'Mesenchymal'
named entity 'MULTIPOTENT'
named entity 'REGENERATIVE'
named entity 'TECHNIQUES'
named entity 'TECHNOLOGY'
named entity 'THEIR'
named entity 'APPROACHES'
named entity 'MSCs'
named entity 'Critical'
named entity 'immunomodulatory'
named entity 'critical illness'
named entity 'illnesses'
named entity 'technology'
named entity 'multipotent'
named entity 'regenerative'
named entity 'phase I'
named entity 'mesenchymal'
named entity 'studies'
named entity 'Application'
named entity 'genetically modified'
named entity 'genetically modified'
named entity 'mesenchymal'
named entity 'critical illness'
named entity 'MSCs'
named entity 'cell therapy'
named entity 'sepsis'
named entity 'Mesenchymal'
named entity 'optimization'
named entity 'prokaryotic'
named entity 'chemokines'
named entity 'therapeutic effects'
named entity 'AAVs'
named entity 'HIF1'
named entity 'permeability'
named entity 'reduction of inflammation'
named entity 'lipids'
named entity 'MSCs'
named entity 'MHC'
named entity 'Homeostasis'
named entity 'lentivirus'
named entity 'MSCs'
named entity 'overexpressing'
named entity 'Minicircles'
named entity 'organ'
named entity 'anti-bacterial'
named entity 'transfected'
named entity 'plasmid DNA'
named entity 'phagocytosis'
named entity 'MSCs'
named entity 'MSCs'
named entity 'gene-editing technology'
named entity 'AAV'
named entity 'microRNA'
named entity 'ALF'
named entity 'CD105'
named entity 'MSCs'
named entity 'acute phase'
named entity 'minicircles'
named entity 'clinical trials'
named entity 'anti-inflammatory'
named entity 'ischemia'
named entity 'MSCs'
named entity 'ischemic'
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