"Bubble Bassets" Cured of Genetic Disorder by In-Vivo Gene Therapy Technique
Tuesday, May 16, 2006
PHILADELPHIA In-vivo gene therapy successfully restored the immune system in basset pups with X-linked severe combined immunodeficiency, or XSCID, a life-threatening genetic disorder that effectively disables the immune system. Researchers from the University of Pennsylvania School of Veterinary Medicine and the National Institute of Allergy and Infectious Disease injected a retrovirus containing a corrective version of the gene responsible for XSCID, an important proof of principle for the technique of "in-vivo" gene therapy. Their findings are presented in the April 15 issue of the journal Blood.
In humans, XSCID affects one in 100,000 boys, resulting from the
inheritance of a faulty gene on one of the mother's X-chromosomes. It
often proves fatal before the child's first birthday. The disease
first came to public attention in the late 1970s with the "Bubble Boy,"
David Vetter, who lived his entire life in a sterilized environment in
order to protect him from outside germs. Vetter died in 1984.
The only treatment for XSCID is through a bone-marrow transplant from a normal donor designed to replenish the hematopoietic stem cells that are capable of constantly renewing new functional immune cells, or,
more recently, gene therapy that works by replacing the defective gene
with a normal gene in the patient’s own cells. Gene therapy has been
put to curative use against this disease in humans resulting in
successful immune reconstitution in 10 of 11 boys in a 1999 French
study. This clinical trial consisted of the standard ex-vivo approach
to gene therapy in which bone-marrow cells were taken out of the body
of the affected boy, cultured in vitro for five days with exposure to a
retroviral vector containing the normal gene and transplanted back into
the patient. Three of the boys unfortunately developed a T-cell
leukemia attributed to the gene therapy resulting in the cessation of
“Although ex-vivo gene therapy has been shown to be capable of
restoring normal immune function in XSCID boys, there are several
potential problems with this approach,” said Peter J. Felsburg,
professor of immunology at Penn's School of Veterinary Medicine. “The number of gene-corrected bone- marrow stem cells that can be
transplanted back into the patient is limited to correcting the
potentially low number of bone-marrow stem cells harvested from the
patient. In addition, the manipulation and culturing of the cells
outside the body may alter their ability to provide for long-term
generation of new immune cells.”
The Penn researchers and their NIAID colleagues, led by Drs. Suk See
Ting-De Ravin and Harry L. Malech took a different approach by directly injecting the retrovirus vector containing the corrective gene into the bloodstream of XSCID dogs with the hope of correcting the defective hematopoietic stem cells within the patient. The therapy completely restored immune function in three of the four dogs the researchers treated. The fourth dog received the lowest dose of the retrovirus vector the virus that had been engineered to pass on the gene leading Felsburg and his colleagues to believe that there is a lower limit to the dose before the treatment becomes effective.
Since the boys involved in the French gene-therapy study did not
develop leukemia until more than three years after the treatment began,
the researchers have been particularly interested in knowing the
long-term consequences of the trial. At 16 and 18 months following
treatment, the two dogs involved in the long-term study have maintained
their immune systems and remain, effectively, cured of XSCID, with no
adverse side effects.
“The results of this study show that this in-vivo approach to gene
therapy may be a viable alternative for not only gene therapy of XSCID
but perhaps other hematologic and immunologic diseases, thereby
eliminating any potential detrimental effects of the ex-vivo
manipulation and culture of cells that is required by current clinical
gene therapy protocols,” Felsburg said. “In addition, this approach
would make it easier to perform gene therapy outside of specialized
Felsburg's research was funded by grants from the National Institute of
Allergy and Infectious Disease of the National Institutes of Health.
Penn's School of Veterinary Medicine is one of the world's premier veterinary schools. Founded in 1884, the School was built on the concept of Many Species, One Medicine. The birthplace of veterinary specialties, the School serves a distinctly diverse array of animal patients, from pets to horses to farm animals at our two campuses. In Philadelphia, on Penn's campus, are the Matthew J. Ryan Veterinary Hospital for companion animals, as well as classrooms, laboratories and the School's administrative offices. The large-animal facility, New Bolton Center, in Kennett Square, Pa., encompasses hospital facilities for the care of horses and food animals as well as diagnostic laboratories serving the agriculture industry. The School has successfully integrated scholarship and scientific discovery with all aspects of veterinary medical education.
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