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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1089/hum.2015.139 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!