2019
DOI: 10.1007/5584_2019_459
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Advancing Mesenchymal Stem Cell Therapy with CRISPR/Cas9 for Clinical Trial Studies

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Cited by 37 publications
(20 citation statements)
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“…Recently, China, USA, Jordon, Iran, and several other countries have begun cell-based therapy clinical studies and some reports have been published (Table 1). Interestingly, one of the available methods to evaluate its efficacy in the maintenance or repair of damaged vital organs is the use of mesenchymal stem cell (MSCs) therapy that widely used in the treatment of type 2 diabetes, autoimmune disease, spinal cord injury, GVHD and several other diseases specially with high immunity rates have been used [23,[26][27][28]. MSCs, using their immunomodulatory properties and their differentiation ability, can prevent lung tissue death by counteracting the cytokine storm and regeneration and reconstruction of damaged tissues (Fig.…”
Section: Msc Clinical Trials For Covid-19mentioning
confidence: 99%
“…Recently, China, USA, Jordon, Iran, and several other countries have begun cell-based therapy clinical studies and some reports have been published (Table 1). Interestingly, one of the available methods to evaluate its efficacy in the maintenance or repair of damaged vital organs is the use of mesenchymal stem cell (MSCs) therapy that widely used in the treatment of type 2 diabetes, autoimmune disease, spinal cord injury, GVHD and several other diseases specially with high immunity rates have been used [23,[26][27][28]. MSCs, using their immunomodulatory properties and their differentiation ability, can prevent lung tissue death by counteracting the cytokine storm and regeneration and reconstruction of damaged tissues (Fig.…”
Section: Msc Clinical Trials For Covid-19mentioning
confidence: 99%
“…CRISPR/Cas9-based gene manipulation has been widely employed in stem cell field particularly MSCs research, including gene knockin, knock-out, activation or silence, etc. CRISPR/Cas9-mediated gene knockdown in MSCs has been proved effective in treating diseases such as myocardial infarction [131]. Targeted gene knock-in promoted the differentiation capacity of MSCs and, in turn, ameliorated the insufficiency of functional cells in local sites [132].…”
Section: Crispr-cas9 Technology To Obtain Highly Homogeneous Mscsmentioning
confidence: 99%
“…Several studies demonstrated that the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas system is highlighted as a simple and effective tool for genetic engineering with applicability to the edition of the mammalian cell genome, and which was tested in clinical trials. It has been recently proposed perspectives on how the CRISPR-Cas system may improve the therapeutic potential of MSCs [239,240]. In this context, there are today the first evidences of successful and effective MSCs secretome managing via CRISPR/Cas9 genome editing technology.…”
Section: Genetic Manipulationmentioning
confidence: 99%