Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer

Neuromuscul Disord. 1995 Jul;5(4):291-5. doi: 10.1016/0960-8966(94)00070-p.

Abstract

We report our experience on myoblast transplantation in three Duchenne muscular dystrophy patients. Pure myoblasts (55 x 10(6) per patient) from HLA-matched donors, were injected into a tibialis anterior and the controlateral muscle was sham injected. Three months after transplantation, biopsies from the injected muscles were negative for dystrophin expression by immunocytochemistry. Reverse transcriptase-PCR (RT-PCR) failed to amplify any fragments of the deleted regions. This result confirms that myoblast transplantation is feasible, although the efficacy of this therapeutic approach is poor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Biopsy
  • Blotting, Western
  • Child
  • DNA / analysis
  • Dystrophin / analysis*
  • Dystrophin / genetics
  • Humans
  • Injections, Intramuscular
  • Male
  • Molecular Sequence Data
  • Muscle Fibers, Skeletal / transplantation*
  • Muscular Dystrophies / therapy*
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • Time Factors

Substances

  • Dystrophin
  • RNA, Messenger
  • DNA