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      Review of the Current Trends in Clinical Trials Involving Induced Pluripotent Stem Cells

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          Graphical Abstract

          In 2006, the induced pluripotent stem cell (iPSC) was presented to the world, paving the way for the development of a magnitude of novel therapeutic alternatives, addressing a diverse range of diseases. However, despite the immense cell therapy potential, relatively few clinical trials evaluating iPSC-technology have actually translated into interventional, clinically applied treatment regimens. Herein, our aim was to determine trends in globally conducted clinical trials involving iPSCs. Data were derived both from well-known registries recording clinical trials from across the globe, and databases from individual countries. Comparisons were firstly drawn between observational and interventional studies before the latter was further analyzed in terms of therapeutic and nontherapeutic trials. Our main observations included global distribution, purpose, target size, and types of disorder relevant to evaluated trials. In terms of nontherapeutic trials, the USA conducted the majority, a large average number of participants—187—was included in the trials, and studies on circulatory system disorders comprised a slightly higher proportion of total studies. Conversely, Japan was the frontrunner in terms of conducting therapeutic trials, and the average number of participants was much lower, at roughly 29. Disorders of the circulatory, as well as nervous and visual systems, were all studied in equal measure. This review highlights the impact that iPSC-based cell therapies can have, should development thereof gain more traction. We lastly considered a few companies that are actively utilizing iPSCs in the development of therapies for various diseases, for whom the global trends in clinical trials could become increasingly important.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s12015-021-10262-3.

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          Most cited references49

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          Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.

          Differentiated cells can be reprogrammed to an embryonic-like state by transfer of nuclear contents into oocytes or by fusion with embryonic stem (ES) cells. Little is known about factors that induce this reprogramming. Here, we demonstrate induction of pluripotent stem cells from mouse embryonic or adult fibroblasts by introducing four factors, Oct3/4, Sox2, c-Myc, and Klf4, under ES cell culture conditions. Unexpectedly, Nanog was dispensable. These cells, which we designated iPS (induced pluripotent stem) cells, exhibit the morphology and growth properties of ES cells and express ES cell marker genes. Subcutaneous transplantation of iPS cells into nude mice resulted in tumors containing a variety of tissues from all three germ layers. Following injection into blastocysts, iPS cells contributed to mouse embryonic development. These data demonstrate that pluripotent stem cells can be directly generated from fibroblast cultures by the addition of only a few defined factors.
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            Induction of pluripotent stem cells from adult human fibroblasts by defined factors.

            Successful reprogramming of differentiated human somatic cells into a pluripotent state would allow creation of patient- and disease-specific stem cells. We previously reported generation of induced pluripotent stem (iPS) cells, capable of germline transmission, from mouse somatic cells by transduction of four defined transcription factors. Here, we demonstrate the generation of iPS cells from adult human dermal fibroblasts with the same four factors: Oct3/4, Sox2, Klf4, and c-Myc. Human iPS cells were similar to human embryonic stem (ES) cells in morphology, proliferation, surface antigens, gene expression, epigenetic status of pluripotent cell-specific genes, and telomerase activity. Furthermore, these cells could differentiate into cell types of the three germ layers in vitro and in teratomas. These findings demonstrate that iPS cells can be generated from adult human fibroblasts.
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              Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies

              The Lancet, 385(9967), 509-516
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                Author and article information

                Contributors
                juji@catholic.ac.kr
                Journal
                Stem Cell Rev Rep
                Stem Cell Rev Rep
                Stem Cell Reviews and Reports
                Springer US (New York )
                2629-3269
                2629-3277
                16 September 2021
                : 1-13
                Affiliations
                [1 ]GRID grid.213910.8, ISNI 0000 0001 1955 1644, Department of Biology, , Georgetown University, ; Washington, DC USA
                [2 ]GRID grid.411947.e, ISNI 0000 0004 0470 4224, CiSTEM Laboratory, Catholic iPSC Research Center, College of Medicine, , The Catholic University of Korea, ; Seoul, Korea
                [3 ]GRID grid.411947.e, ISNI 0000 0004 0470 4224, Division of Rheumatology, Department of Internal Medicine, St. Mary’s Hospital, Institute of Medical Science, College of Medicine, , The Catholic University of Korea, ; Seoul, Korea
                Author information
                http://orcid.org/0000-0002-1381-5466
                Article
                10262
                10.1007/s12015-021-10262-3
                8445612
                34532844
                7b7eed41-9007-4cb8-a0e0-d3381f746e1d
                © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 9 September 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100002701, ministry of education;
                Award ID: NRF-2021R1C1C2004688
                Award ID: NRF-2019R1A2027588
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003625, ministry of health and welfare;
                Award ID: HI16C2177
                Award ID: HI20C0495
                Award Recipient :
                Categories
                Article

                clinical trials,induced pluripotent stem cells,cell therapy,interventional,therapeutic,nontherapeutic,allogeneic,autologous

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