| HAIFA, Israel--(BUSINESS WIRE)--Pluristem Life Systems, Inc. (OTCBB:
PLRS -
News), a cell
therapy company dedicated to the commercialization of stem cell
products, announces promising final results of an animal model study
which could benefit 100,000 blood cancer patients annually. PLX-BMT, the
Company's innovative adjuvant cell therapy product is based on Placenta
Expanded Mesenchymal cells. It intended to resolve the global shortfall
of matched tissue for blood cancer patients requiring bone marrow
transplantation by improving the engraftment of Umbilical Cord Blood
(UCB). The Pre-Clinical results document that adding Pluristem's PLX-BMT
to UCB stem cells during the Bone Marrow Transplant (BMT) human cell
engraftment in NOD SCID mice showed up to a 500% increased engraftment
after irradiation and Chemotropic treatment. BMT traditionally treats
patients whose bone marrow has been damaged by chemotherapy, or certain
genetic diseases that lead to anemia, leukemia, lymphomas, autoimmune
disease and other blood-related disorders. Its effectiveness is severely
limited because of the lack of a matching donor or shortage of UCB stem
cells engrafted during the procedure. If additional animal studies and
human clinical trials prove equally successful as this first
Pre-Clinical, Pluristem's PLX-BMT product with 500% increased engraftment
could lead to more Bone Marrow Transplants (BMT) for these types of
blood cancers.
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 (HSC) to engraft in mouse bone marrow
and to simulate the recovery of the human's Hematological system.
50,000-100,000 human UCB derived CD34+ cells (hUCB CD34+) were injected
into the tail vein of NOD-SCID mice along with 0.5*106 PLX I cells.
After periods of 28-32 days, mice were sacrificed and the marrow was
analyzed. Human cell engraftment was performed in both sub lethally
irradiated (350 Rad) and chemotherapy administrated (50 mg/kg Busulfan)
mice. FACS analysis of human CD45 positive cells in mice bone marrow
demonstrated an increscent of cell engraftment in part of the
experimental animals up to 5 folds compared to mice transplanted with
CD34+ cells only.
Mr. Zami Aberman, CEO, stated, "Co-transplantation of PLX-BMT cell
types may be a promising manipulation improving cord blood performance
during the bone marrow transplants in adults blood disorder. The
pre-clinical results suggest blood disorder treatment is being improved
by using MSC derived from placenta and expanded in Pluristem's 3D
bioreactor in combination with UCB derived HSC. We strongly believe that
PLX-BMT can change the clinical process now being used to treat blood
cancer and could eventually save millions of lives."
About Pluristem
Pluristem Life Systems, Inc. is a life sciences driven company that is
developing and commercializing stem cell expansion technology products
for the treatment of severe blood disorders. The Company is discovering
and developing cell-based therapeutics that utilizes adult stem cells
expanded in a proprietary bioreactor mimicking 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.
Its first adult stem cell product targets a critical global shortfall of
matched tissue for bone marrow transplantation since bone marrow
transplantation is often the only cure for patients suffering from
leukemia, lymphoma, myeloma and many other hematological diseases. The
Company has made a strategic decision to work only with adult stem cells
since the practical use of embryonic stem cells is severely restricted
by various religious, ethical and legal considerations.
http://www.pluristem.com
Safe Harbor Statement
This press release contains statements, which may constitute
"forward-looking statements" regarding our intent, belief or current
expectations. Forward-looking statements in this release include
statements: results of our animal model study could benefit 100,000
blood cancer patients annually; that PLX-1 is intended to resolve the
global shortfall of matched tissue for blood cancer patients requiring
bone marrow transplantation by improving the engraftment of Umbilical
Cord Blood (UCB); that if additional animal studies and human clinical
trials prove equally successful as this first Pre-Clinical, Pluristem's
PLX-BMT product with 500% increased engraftment could lead to more Bone
Marrow Transplants (BMT) for these types of blood cancers; the
pre-clinical results suggest blood disorder treatment is being improved
by using MSC derived from placenta and expanded in Pluristem's 3D
bioreactor in combination with UCB derived HSC; and we believe that PLX-BMT
can change the clinical process now being used to treat blood cancer and
could eventually save millions of lives. 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 pre-clinical
trials results may not be able to be successfully duplicated in clinical
trials; 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.
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