| Literature DB >> 26652770 |
Elisa Negroni1, Anne Bigot1, Gillian S Butler-Browne1, Capucine Trollet1, Vincent Mouly1.
Abstract
Cell-based therapy for muscular dystrophies was initiated in humans after promising results obtained in murine models. Early trials failed to show substantial clinical benefit, sending researchers back to the bench, which led to the discovery of many hurdles as well as many new venues to optimize this therapeutic strategy. In this review we summarize progress in preclinical cell therapy approaches, with a special emphasis on human cells potentially attractive for human clinical trials. Future perspectives for cell therapy in skeletal muscle are discussed, including the perspective of combined therapeutic approaches.Entities:
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Year: 2016 PMID: 26652770 DOI: 10.1089/hum.2015.139
Source DB: PubMed Journal: Hum Gene Ther ISSN: 1043-0342 Impact factor: 5.695