12-18-2001
Contact:
Michael Robb
michael.robb@ualberta.ca
780-492-0647
University
of Alberta
A
team of University of Alberta researchers has successfully created a mouse model
that scientists can now use to test antiviral therapies against Hepatitis C, a
contagious viral disease that usually leads to serious, permanent liver damage.
The disease afflicts about 175 million around the world.
"This
is certainly a major advance in the fight against the disease," says Dr.
David Mercer, the lead author of the scientific paper published in this month's
Nature Medicine journal. "We now have a viable way of testing new drugs
which might ultimately help lead to development of a cure."
"The
development of effective therapeutic strategies has been significantly hampered
for more than a decade by difficulties in establishing in vitro and in vivo
models of viral replication," says principal investigator Dr. Norman
Kneteman, a professor of surgery at the U of A. "We've solved that
problem."
Essentially,
the researchers have transplanted human liver cells into a genetically-modified
mouse; the transplanted cells then begin rapidly dividing and fill up much of
the mouse liver. These "chimeric" mice can be infected with the
hepatitis C virus, whereas previously only humans and chimpanzees have been
susceptible to hepatitis C.
"Not
only does the new mouse model give researchers the ability to test new
therapies," says co-principal investigator Dr. Lorne Tyrrell, "it also
allows researchers to study questions hitherto impossible to study, such as how
the virus infects healthy cells and how the virus replicates."
"This
advance opens the floodgates on basic and applied research," says Dr.
Tyrrell, whose previous work on the hepatitis B virus led to the development of
a revolutionary new drug proven to be an effective treatment for Hepatitis B.
Hepatitis
C affects an estimated 175 million people worldwide, including approximately 3
million Americans and 300,000 Canadians. Infection leads to chronic liver
disease in 70 to 80 percent of patients, with 30 percent developing cirrhosis,
and five to ten percent cancer of the liver.
Liver
failure secondary to long-term hepatitis C infection is the number one reason
for liver transplantation in North America. There is no vaccination against
hepatitis C, and current treatment using combinations of interferon and
ribavirin works only in a selected number of patients.