
HepaLife Announces Scientific Presentation Of PBS-1 Cell Line At
International Influenza Meeting
HepaLife’s patented PBS-1 cell line shown to outperform
current cell system by 500% on average; PBS-1 cells are capable
of growing human and avian influenza virus to extremely high titers,
are free of any exogenous agents, are non-tumorigenic and are readily
adaptable to a variety of culture conditions
Boston, MA – May 29, 2007 - HepaLife Technologies,
Inc. (OTCBB: HPLF) (FWB: HL1) (WKN: 500625) is pleased to announce
a scientific presentation of its cell based PBS-1 technology for
potential influenza vaccine production at the “Options
for the Control of Influenza VI Conference,” to be held June
17-23, 2007, in Toronto, Canada .
Entitled “High titer growth of human and avian influenza viruses
in an immortalized chick embryo cell line without the need for exogenous
proteases,” and presented by K.A. Smith, from Michigan State
University, the poster presentation will cover recent research results
of the PBS-1 cell line and, among other things, challenges of current
influenza vaccine production methodologies, which rely on embryonated
chick eggs, and concerns over existing cell lines, which all require
the addition of exogenous agents.
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. In recent tests, 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 at substantially
higher levels than the research community’s widely-used current
model, primary chick kidney cells.
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.
In previous tests, the PBS-1 cells on average functioned five times
better than primary chick kidney cells, and in some cases, outperformed
them by 150-fold. Influenza viruses grown in PBS-1 cells are released
into the culture fluid without the need for exogenous proteases,
thus simplifying downstream processing. Additionally, PBS-1 cells
are free of any exogenous agents, are non-tumorigenic, and are readily
adaptable to a variety of culture conditions, including growth on
microcarrier beads.
(For more information on recent research findings, please click
on the following links:
http://www.hepalife.com/20070328-1.html.php
or
http://www.hepalife.com/20070122-1.html.php)
Protected by five issued patents, HepaLife is developing production
methods to make flu vaccines faster, safer and at less cost by means
of the Company’s patented PBS-1 line of cells.
HepaLife’s non-mammalian PBS-1 cell line is derived from an
immortalized chicken embryo cell, and is being developed for more
flexible cell-culture based vaccine production with the ability to
quickly address prospective mutations in the avian influenza virus.
(View
a CBS-affiliate, WWMT, television news story about HepaLife’s
active cell-based vaccine research)
ABOUT HEPALIFE TECHNOLOGIES, INC.
HepaLife Technologies, Inc. (OTCBB: HPLF - News; FWB: HL1) (WKN:
500625) is a development stage biotechnology company focused on the
identification, development and eventual commercialization 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) cell-culture based vaccines 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/20070529-1.html.php
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