HAIFA, Israel--(BUSINESS WIRE)--July 5, 2006--Pluristem Life Systems,
Inc. (OTCBB:PLRS
- News), a cell
therapy company dedicated to the commercialization of stem cell
products, today announced promising initial results of an animal model
study using the company's innovative adjuvant cell therapy product known
as PLX-1. PLX-1, by adding Mesenchymal Stromal Cells (MSC) during bone
marrow transplant procedures that use umbilical cord blood (UCB)
samples, is intended to offer a breakthrough solution to improved
engraftment of blood-producing Hematopoeitic Stem Cells (HSC)
The preliminary results suggest that the use of Mesenchymal
Stromal Cells (MSC), in combination with Umbilical Cord Blood (UCB)
derived Hematopoeitic Stem Cells (HSC) can improve the treatment of
blood disorders.
The animal studies were performed on immune-deficient NOD SCID mice
following systemic myeloablation of their bone marrow to simulate the
BMT clinical protocol. This in-vivo model is based on the known ability
of human Hematopoietic stem cells to engraft in mouse bone marrow and to
enable recovery of the mouse's immune system. This assay is well known
and
The results showed that when human UCB samples were transplanted
together with PLX 1 into NOD SCID mice, the amount of engrafted cells
was from 2-4 times greater than when transplants were carried out with
UCB samples lacking PLX 1.
If additional animal studies and human clinical trials prove equally
successful, PLX-BMT could lead to wider use of bone marrow transplants in
various types of blood cancer. Nearly 100,000 people could benefit from
this treatment annually.
Transplants of HSC derived from UCB are a novel alternative to
conventional bone marrow transplants and have several unique advantages,
in spite of their present quantitative limitations. PLX 1 transplanted
together with limited number of HSC from UCB increase the effectiveness
of the HSC dose and, if clinically proven, may be used as a replacement
of bone marrow transplants in adults, eliminating the frustrated process
of matched Bone Marrow donor finding.
In the PLX-1 study, 9 NOD/SCID mice received PLX-BMT with HSC from UCB, 5
of the control group did not. The injections of PLX 1 together with HSC
from UCB (selected positive CD34 cells) into the blood system of the
mice increased 2-4 times the engraftment after four weeks. The high
level of engraftment was evident in the 9 treated NOD SCID mice by the
presence of 2- 13 % human CD45 cells. This reflects the reconstruction
of the mouse immune system and thus, the success of the procedure and
the significant advantage of transplantation in the presence of PLX-1
along with CB derived hematopoietic stem cells
In contrast, the 5 NOD SCID mice in the control group that received UCB
without the PLX 1 showed only a 1-3 % presence of human CD45 cells.
This result shows that adding PLX-BMT to the implantation process can
improve dramatically the engraftment rate of stem cells.
Mr. Zami Aberman, CEO, stated, "We believe that the advantages in use of
umbilical cord blood hematopoietic stem cells, combined with our PLX 1
products could have the potential to change the way bone marrow
transplants are conducted in the future."
About Pluristem:
Pluristem Life Systems, Inc. is a cell therapy company dedicated to the
commercialization of stem cell therapy products for the treatment of
severe blood disorders. Pluristem is discovering and developing
cell-based therapeutics utilizing adult stem cells expanded in a
proprietary bioreactor that mimics different naturally occurring
physiological environments. Pluristem expects its first products to be
cell grafts that will provide an efficient and superior alternative to
the standard procedure of bone marrow transplantation to treat blood
cancer and other blood disorders.
Safe Harbor Statement
This press release contains statements, which may constitute
"forward-looking statements". Those statements include statements
regarding the intent, belief or current expectations of Pluristem Life
Systems, Inc., and members of our management as well as the assumptions
on which such statements are based. Forward-looking statements in this
release include statements that we have had promising initial results of
an animal model study; that PLX-1 is intended to offer a breakthrough
solution to improved engraftment during bone marrow transplant
procedures; that preliminary results show PLX-1 can improve the
engraftment rate of HSC and can improve the treatment of blood disorders
; that PLX-BMT could lead to wider use of bone marrow transplants in
various types of blood cancer ; that preliminary results of the PLX-1
study can continue in real life settings; that nearly 100,000 people
could benefit from this treatment annually; that our process may be used
as a replacement of bone marrow transplants in adults; that there is a
significant advantage of transplantation in the presence of PLX-1 along
with CB derived Hematopoietic stem cells; that adding PLX-BMT to the
implantation process can improve dramatically the engraftment rate of
human adult stem cells; that our process has the potential to change the
way bone marrow transplants are conducted in the future.
and that Pluristem expects its first products to be cell grafts that
will provide an efficient and superior alternative to the standard
procedure of bone marrow transplantation to treat blood cancer and other
blood disorders .. Factors which may significantly change or prevent our
forward looking statements from fruition include that we may be
unsuccessful in developing any products; that our technology may not be
validated as we progress further and our methods may not be accepted by
the scientific community; that we are unable to retain or attract key
employees whose knowledge is essential to the development of our
products; that unforeseen scientific difficulties develop with our
process; that results in the laboratory do not translate to equally good
results in real surgical settings; that our patents are not sufficient
to protect essential aspects of our technology; that competitors may
invent better technology; that our products may not work as well as
hoped or worse, that our products may harm recipients; and that we may
not be able raise funds for development or working capital when we
require it. As well, our products may never develop into useful products
and even if they do, they may not be approved for sale to the public.
For further risk factors see the Company's latest 10-KSB filed with the
SEC.
For more information visit our website at
www.pluristem.com
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