METHOD OF GRAFTING GENETICALLY MODIFIED CELLS TO TREAT DEFECTS, DISEASE OR DAMAGE OF THE CENTRAL NERVOUS SYSTEM

摘要

Methods of genetically modifying donor cells by gene transfer for grafting into the central nervous system to treat diseased or damaged cells are disclosed. The modified donor cells produce a molecule capable of affecting the recovery of cells in the CNS. Methods and vectors for carrying out gene transfer and grafting are described.