
HepaLife’s Patented ‘PBS-1’ Cells
for Avian Flu Vaccines Outperform Current Cell System by 500%.
In tests of human influenza viruses received
from the Centers for Disease Control, HepaLife’s PBS-1 cells
outperform widely-used ‘primary chick kidney cell’ system
by an average of 500%, and in some cases, by as much as 150-fold!
Boston, MA – March 28, 2007 - HepaLife
Technologies, Inc. (OTCBB: HPLF) (FWB: HL1) (WKN: 500625) today announced
that the Company’s patented ‘PBS-1’ cells,
under development for influenza vaccine production, have successfully
replicated numerous human influenza virus strains received from the
Centers for Disease Control (CDC) at substantially higher levels
than the research community’s widely-used current model, primary
chick kidney cells.
“The single most important step towards the
production of a cell-culture based vaccine against a targeted virus
is the ability to grow the same virus in a cell substrate. Today’s
announcement clearly demonstrates that not only are HepaLife’s
PBS-1 cells capable of replicating some of the most active and significant
human influenza viruses in the world, but our cells are also far
superior, in some cases outperforming the traditional research cell
system model by as much as 150-fold,” explained HepaLife President
and CEO, Mr. Frank Menzler.
The ability to replicate virulent human viruses
received from the CDC inside HepaLife’s PBS-1 cells, is a very
important step towards the use of the cell line in cell-based vaccine
production, a faster, cheaper, and more flexible technology for producing
influenza vaccines in response to constantly evolving virus strains.
(View HepaLife’s January 22, 2007 press release,
announcing that the Company’s PBS-1 cells successfully replicate
H1N1, H3N2, and type-B viruses at:
http://www.hepalife.com/20070122-1.html.php )
A US Government report issued by the Department
of Health and Human Services has reiterated earlier warnings of the
avian flu's pandemic threat, and among its response recommendations,
urged cell-culture based influenza vaccine production, HepaLife's
primary application for its patented 'PBS-1' cell line.
Cell-culture based vaccine production with the ability
to quickly address prospective mutations in the avian influenza virus
is a promising replacement of cumbersome, time-consuming, and costly
vaccine production processes which currently rely on chicken eggs.
In the event of a flu pandemic, the traditional egg-based process
is unlikely to produce vaccines fast enough to meet expected demand.
HepaLife’s PBS-1 Cells Outperform Others in Tests of Highly
Potent Influenza Viruses Received from the Centers for Disease
Control (CDC)
In recent lab tests, HepaLife’s patented PBS-1
cells successfully amplified several strains of human influenza viruses
received from the Centers for Disease Control. On average,
PBS-1 cells functioned five times better than the research community’s
widely-used, ‘primary chick kidney cells’, and in some
cases, outperformed them by 150-fold.
Importantly, among the viruses successfully tested
were three specific strains deemed currently most threatening by
the World Health Organization and the U.S. Food and Drug Administration. These
viruses were selected for development of the inactivated influenza
vaccines prepared for the 2006-2007 influenza season.
“These results are astounding,” explained
Dr. Paul Coussens, a HepaLife Scientific Advisory Board Member and
Professor of Molecular Biology and Molecular Virology. “Most
interestingly, these research results suggest that PBS-1 cells could
allow for manufacture of vaccines that are much more similar to the
actual viruses circulating in humans during any given year, since
HepaLife’s successfully tested influenza strains from the CDC
are all recent human isolates which are unmodified.”
“Surprisingly, these same influenza strains
either grow very poorly or not all in commonly used cell lines, such
as MDCK and VERO cells,” continued Dr. Coussens. “The
research outcomes however, are even more encouraging when considering
that PBS-1 successfully replicated these viruses without the addition
of Trypsin, a protease often used to help cleave various influenza
viruses from other cell types, such as MDCK or VERO cells.”
“These outstanding performance results cover
a wide range of virus strains, and further highlight the exciting
potential for HepaLife’s PBS-1 cell technology platform to
increase efficiency and simplify downstream cell-culture based vaccine
production, a system that is more cost-effective, flexible and responsive
than traditional egg-based methods,” concluded Mr. Frank Menzler.
Currently, vaccine production involves injecting
a small amount of a targeted virus into fertilized chicken eggs. Over
time, the virus is harvested from the eggs, eventually inactivated
and purified, and finally blended into a vaccine and bottled in vials. Fertilized
eggs require approximately six months from order to delivery, with
the total egg-based production method requiring about 12 months.
In the event of a flu pandemic, it is unlikely to produce vaccines
fast enough to meet expected demand.
HepaLife’s PBS-1 cell technology platform
was recognized in a report by Frost & Sullivan and broadcast
by the CBS-affiliate, WWMT-TV News. To review the report and view
the television news story, please visit www.hepalife.com.
ABOUT HEPALIFE TECHNOLOGIES, INC.
HepaLife Technologies, Inc. (OTCBB: HPLF - News;
FWB: HL1) (WKN: 500625) is a biotechnology company focused on the
identification and development of cell-based technologies and products.
Current cell-based technologies under development
by HepaLife include 1) the first-of-its-kind artificial liver device,
2) proprietary in-vitro toxicology and pre-clinical drug testing
platforms, and 3) novel cell-culture based vaccine production to
protect against the spread of influenza viruses among humans, including
potentially the high pathogenicity H5N1 virus.
For additional information, please visit www.hepalife.com.
To receive future press releases via email, please
visit:
http://www.hepalife.com/investor-alerts.php
To view the full HTML text of this release, please
visit:
http://www.hepalife.com/20070328-1.html.php
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