CEL-SCI Files Patent Application to Support Company's Treatment for More Virulent Strain of H1N1 Swine and Other Influenza Virus
24 6월 2009 - 10:25PM
PR Newswire (US)
VIENNA, Va., June 24 /PRNewswire-FirstCall/ -- CEL-SCI CORPORATION
(NYSE AMEX: CVM) announced today that it has filed a provisional
U.S. patent application covering its L.E.A.P.S.(TM) immune therapy
drugs (vaccines) for the prevention/treatment of H1N1, swine, bird
flu, Influenza A and/or evolving mutants or variants of these
viruses. Some experts believe that by the next flu season the swine
flu virus will have evolved and/or combined with other viruses to
create a much more lethal new virus. That is what happened in the
case of the Spanish flu pandemic. CEL-SCI's efforts to fight this
virus are focused on using conserved epitopes from essential
proteins to be found in the A influenza virus for H1N1, H1N5,
swine, bird flu and Spanish influenza to create an effective
vaccine/treatment that could potentially fight such a mutant virus.
Geert Kersten, Chief Executive Officer of CEL-SCI said, "By filing
this provisional patent in the U.S., we are preserving our rights
to file patents on these inventions and for their use world-wide
either as an injected vaccine before a person is infected or
exposed or as a therapeutic vaccine for treatment." Experimental
work has been initiated on these various methods of use and
applications for the A influenza vaccines. These L.E.A.P.S.
vaccines, when used individually or together, are expected to
induce antigen specific immune response(s) which, based on other
L.E.A.P.S. animal tests in multiple disease models will hopefully
lead to a protective immune response. The most recent such
presentation by an outside university investigator (Dr. Borthakur,
University of Hawaii) reported new L.E.A.P.S. Tuberculosis data at
the Annual American Society for Microbiology in Philadelphia, PA.
This TB data demonstrated that vaccines utilizing the L.E.A.P.S.
vaccine technology with specificity for particular Mycobacterium
tuberculosis (TB) antigens can elicit immune responses that would
be expected to be protective against tuberculosis and have the
potential to treat swine and other H1N1 influenzas. The TB
investigators presented data that showed that blood and spleen
cells from immunized mice produced gamma interferon in response to
the vaccine, while the cells from mice in the various control
groups did not. Other recent L.E.A.P.S. data, presented by Dr.
Kenneth S. Rosenthal, Professor of Microbiology, Immunology and
Biochemistry at Northeastern Ohio Universities Colleges of Medicine
and Pharmacy and colleagues at the 12th NFID meeting in Baltimore
showed that CEL-SCI's L.E.A.P.S. vaccines can activate and cause
human blood monocyte cells to become dendritic cells that secrete
the IL-12 cytokine. The dendritic cells that result initiate a
protective cell mediated and antibody immune response. These
results were obtained for L.E.A.P.S. vaccines against herpes
simplex and HIV. The L.E.A.P.S. technology is a novel T-cell
modulation platform technology that enables CEL-SCI to design and
synthesize proprietary immunogens. Any disease for which an
antigenic sequence has been identified, such as infectious,
parasitic, malignant or autoimmune diseases and allergies, are
potential therapeutic or preventive sites for the application of
L.E.A.P.S. technology. Each L.E.A.P.S. construct is composed of a T
cell binding ligand (TCBL) which has previously demonstrated the
ability to induce and elicit protective immunity and antigen
specific antibody production in animal models. The concept behind
the L.E.A.P.S. technology is to directly mimic cell/cell
interactions on the dendritic and T-cell surface with synthetic
peptides. The L.E.A.P.S. constructs containing the antigenic
disease epitope linked to an Immune/T-cell binding ligand (I/TCBL)
can be manufactured by peptide synthesis or by covalently linking
the two peptides. Depending upon the type of L.E.A.P.S. construct
and I/TCBL used, CEL-SCI is able to direct the outcome of the
immune response towards the development of T-cell function with
primarily effector T-cell functions (T Lymphocyte; helper/effector
T lymphocyte, type 1 or 2 [Th1 or Th2], cytotoxic [Tc] or
suppressor [Ts]). The L.E.A.P.S. vaccine constructs are chimeric
peptides which combine antigen specificity with immune response
modulation. CEL-SCI Corporation is developing products that empower
immune defenses. Its lead product is Multikine(R) which is
currently being readied for a global Phase III trial. The Company
has operations in Vienna, Virginia, and Baltimore, Maryland. When
used in this report, the words "intends," "believes," "anticipated"
and "expects" and similar expressions are intended to identify
forward-looking statements. Such statements are subject to risks
and uncertainties which could cause actual results to differ
materially from those projected. Factors that could cause or
contribute to such differences include, an inability to duplicate
the clinical results demonstrated in clinical studies, timely
development of any potential products that can be shown to be safe
and effective, receiving necessary regulatory approvals,
difficulties in manufacturing any of the Company's potential
products, inability to raise the necessary capital and the risk
factors set forth from time to time in CEL-SCI Corporation's SEC
filings, including but not limited to its report on Form 10- K/A
for the year ended September 30, 2008. The Company undertakes no
obligation to publicly release the result of any revision to these
forward-looking statements which may be made to reflect the events
or circumstances after the date hereof or to reflect the occurrence
of unanticipated events. DATASOURCE: CEL-SCI Corporation CONTACT:
Gavin de Windt of CEL-SCI Corporation, +1-703-506-9460 Web Site:
http://www.cel-sci.com/
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