Altamira Therapeutics’ Peptide-Based Delivery Platform Shown to Enhance Potency of Commonly Used Gene Delivery Method as Published in Peer-Reviewed Journal
07 Febrero 2024 - 7:47AM
- Independent peer-reviewed study shows enhanced cell
transduction with adeno-associated virus (AAV) vectors, commonly
used in gene therapy, when integrating Altamira’s peptide-based
delivery technology
- Increased potency may help to reduce AAV immunogenicity and
resistance to AAVs in certain cell types
HAMILTON, BERMUDA, Feb. 7, 2024 -- Altamira
Therapeutics Ltd. (Nasdaq: CYTO) ("Altamira" or the
"Company"), a company providing nanoparticle-based technology for
efficient RNA delivery to extrahepatic targets, announced today the
publication of a peer-reviewed article in the Journal of
Integrative Medicine titled, "Melittin analog p5RHH enhances
recombinant adeno-associated virus transduction efficiency". This
work evaluates the use of various peptides to enhance
adeno-associated virus (AAV) cell transduction and was conducted by
an independent research group.1 Recombinant AAVs are commonly used
as carriers to introduce nucleic acids in cells for gene therapy;
several AAV-based gene therapy drugs have already been approved by
the U.S. Food and Drug Administration (FDA).
The study sought to find ways of increasing the
endosomal release of AAV-based therapeutics by using peptides
derived from melittin, a component of bee venom known for its
ability to permeabilize biological membranes. The research group
evaluated 76 melittin derivatives, including p5RHH, the peptide
underlying Altamira’s OligoPhore™ / SemaPhore™ nanoparticle
platform for RNA delivery. The scientists discovered that insertion
of p5RHH into the AAV vector (p5RHH-rAAV) not only enhanced cell
transduction, but also succeeded in transducing cell lines
typically considered resistant to AAVs. Further, an in vivo study
in mice showed that the addition of p5RHH to the AAV capsid of
several AAV serotypes significantly enhanced liver transduction
compared to non-modified AAV vectors, observed up to the last time
point four weeks after systemic administration.
“The study results once again highlight the
strong capability of our technology to promote the release of
nucleic acids from the endosome into the cytoplasm, which has
remained a key limiting factor for both non-viral vectors and
viral-derived delivery vehicles such as AAVs,” commented Covadonga
Pañeda, Ph.D., Altamira Therapeutics’ Chief Operating Officer.
“Better transduction efficiency means that lower doses of AAVs may
be used, which could lower the risk for deleterious immune
responses and increase the safety of AAV-based vectors. In
addition, the integration of the p5RHH peptide into different
serotypes of AAV vectors may open new possibilities in AAV-based
gene therapy in cells and tissues that are not typically amenable
to AVV transduction.”
About Altamira Therapeutics
Altamira Therapeutics (Nasdaq: CYTO) is
developing and supplying peptide-based nanoparticle technologies
for efficient RNA delivery to extrahepatic tissues (OligoPhore™ /
SemaPhore™ platforms). The Company currently has two flagship siRNA
programs using its proprietary delivery technology: AM-401 for KRAS
driven cancer and AM-411 for rheumatoid arthritis, both in
preclinical development beyond in vivo proof of concept. The
versatile delivery platform is also suited for mRNA and other RNA
modalities and made available to pharma or biotech companies
through out-licensing. In addition, Altamira holds a 49% stake
(with additional economic rights) in its commercial-stage legacy
asset Bentrio®, an OTC nasal spray for allergic rhinitis. Further,
the Company is in the process of partnering / divesting its inner
ear legacy assets (AM-125 nasal spray for vertigo; post Phase 2;
Keyzilen® and Sonsuvi® for tinnitus and hearing loss; Phase 3).
Founded in 2003, Altamira is headquartered in Hamilton, Bermuda,
with its main operations in Basel, Switzerland. For more
information, visit: https://altamiratherapeutics.com
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1 Meng et al. (2024), Melittin analog p5RHH enhances recombinant
adeno-associated virus transduction efficiency, J Integr Med, in
press.
Contact
Investor Contact:
Hear@altamiratherapeutics.com
800-460-0183
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