Somatic cell gene therapy
AssigneeThe Salk Institute for Biological Studies
InventorsInder Mohan Verma, Daniel Claude St. Louis
Life of this patent
Estimating the term…
Loading patent…
AssigneeThe Salk Institute for Biological Studies
InventorsInder Mohan Verma, Daniel Claude St. Louis
Estimating the term…
The present invention is a somatic cell gene therapy method that is especially useful for the treatment of certain diseases that are caused by gene defects. According to the invention, fibroblast cells are transduced so that they express a “replacement” gene of interest. These transduced fibroblasts are preferably fixed in vitro in an extracellular matrix, and then implanted in the loose connective tissue of the skin of an individual or animal to be treated. Because the fibroblasts are implanted in a highly vascularized compartment of the skin i.e., loose connective tissue of the dermis, the transduced cells, and thus their “replacement” gene products, have direct access to the circulatory system. As a result the needed replacement gene products can easily and efficiently be distributed to other parts of the body. When the gene therapy is no longer needed, the implanted fibroblasts can be conveniently removed.
A gene therapy method comprising:
Transduced primary fibroblasts contained in a collagen matrix suitable for implantation into the loose connective tissue of the dermis of a subject, wherein said transduced fibroblasts are infected with a recombinant retroviral vector that contains exogenous genetic material encoding a gene product, wherein said transduced fibroblasts express said gene product, and wherein expression of said gene product is under the control of a constitutive promoter.
A method for immunizing a subject against immunogenic, exogenous material, said method comprising:
Dependencies are inferred from the claim text.