2015
DOI: 10.2217/nmt.15.2
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Stem Cell Treatments for Neurodegenerative Diseases: Challenges from a science, Business and Healthcare Perspective

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Cited by 9 publications
(4 citation statements)
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“…Emerging studies have suggested that stem cell‐based therapies may be a new intervention for neurodegenerative diseases . The success of stem cell therapy may largely depend on high‐efficient supply of desired functional cell types .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Emerging studies have suggested that stem cell‐based therapies may be a new intervention for neurodegenerative diseases . The success of stem cell therapy may largely depend on high‐efficient supply of desired functional cell types .…”
Section: Introductionmentioning
confidence: 99%
“…Emerging studies have suggested that stem cell‐based therapies may be a new intervention for neurodegenerative diseases . The success of stem cell therapy may largely depend on high‐efficient supply of desired functional cell types . However, the limited supply of required stem cells, low‐efficient conversion technologies, unstable genetic manipulation, and complex ethical controversies are the main challenges in the field .…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, the development and production cost of this technologies will be reflected on the therapeutical option final price. Thereafter, is expected that the fees for stem cell-based therapy for neurodegenerative diseases will be between USD 30.000 and USD 100.000 for each patient [113]. These analyses reasonably prospect that, for now, these therapeutic approaches will be remain unavailable for a large number of patients but, with the progressive improvement of technological process, drug development costs will be reduced, allowing an increased number of subjects the access to these promising therapeutic options.…”
Section: Discussionmentioning
confidence: 99%
“…A possible solution proposed by Yamanaka is the creation of human stem cell banks for therapeutic use, where a standard matrix of different cell lines containing the main HLA types, are available and can be tolerated by 80% of the population. Thus it is intended to reduce the deriving and testing time in each patient, alleviate histocompatibility problems and reduce therapy costs [88] (Table 2). Another important problem to be solved in hiPS cells is the observation of mutations in some of the cell lines, which were not present in the original patient fibroblasts; probably due to the reprogramming process itself [89].…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%