In this communication, we will review the problems caused by cell-mediated
gene therapy taking skeletal muscle as a physiological model. In particular
we have utilised vectors transferring telomerase under the control of retr
oviral promoters into human satellite cells. The set of results presented h
ere has several implications regarding gene therapy trials. Nevertheless, m
ore experiments will be required to fully validate this cellular model and
to use telomerase to safely extend the lifespan of putative gene therapy ve
ctors.