Reuters Health Information: Herbal remedy shows early promise as HCV prophylaxis
Herbal remedy shows early promise as HCV prophylaxis
Last Updated: 2014-11-20
By David Douglas
NEW YORK (Reuters Health) - Saikosaponin b2 (SSb2) extracted
from Bupleurum kaoi root, a traditional liver disease remedy,
can block hepatitis C virus (HCV) entry into cells, according to
Canadian and Taiwanese researchers.
"Since new therapies against hepatitis C are extremely
expensive, we believe SSb2 may be of value as a cost-effective
anti-HCV agent for the management of hepatitis C, particularly
in the liver transplant setting," said Dr. Christopher D.
Richardson of Dalhousie University in Halifax.
However, he told Reuters Health by email, "We are being
cautious since SSb2 is in very early development within the
laboratory."
Dr. Richardson and colleagues used infectious HCV culture
systems to examine the effect of SSb2 and other saikosaponins on
the complete virus life cycle. They also examined the antiviral
activity of the substances against various HCV genotypes,
clinical isolates, and infection of primary human hepatocytes.
"In particular, we identified SSb2 as an efficient inhibitor
of early HCV entry, including neutralization of virus particles,
preventing viral attachment, and inhibiting viral entry/fusion,"
the researchers write in the Journal of Hepatology, online
November 3.
SSb2 also showed activity against various HCV genotypes and
blocked HCV infection of primary human hepatocytes, they say.
SSb2 does not appear to disrupt cell membranes and
accumulate within the host cell, indicating that the
extracellular virus is its target. The researchers suggest that
"SSb2 mediates its antiviral effects, at least in part, by
acting on HCV glycoproteins during the initial stages of
infection."
"Our data support the need for further pre-clinical
investigation of SSb2 for use in prophylactic or combination
therapies against HCV infection," Dr. Richardson said.
"Furthermore, its structure could serve as a lead compound for
future anti-HCV drug development."
SOURCE: http://bit.ly/1F6xCzW
J Hepatol 2014.
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