Altamira Therapeutics’ SemaPhore Delivery Platform Shows Significant Synergis-tic Effects of ZBTB46 mRNA with PD1 Immunotherapy in Control of Tumor Growth in Animal Model
22 Marzo 2023 - 6:47AM
- Preprint of results from animal study shows restriction of
tumor growth in mice treated with ZBTB46 mRNA nanoparticles based
on Altamira’s SemaPhore™ delivery technology
- Nanoparticle treatment combined with immune checkpoint
inhibitor results in synergistic control of tumor growth
Altamira Therapeutics ("Altamira" or the
"Company") (Nasdaq:CYTO), a company dedicated to developing
RNA-based therapeutics that address important unmet medical needs,
today announced the release of animal data by a Washington
University School of Medicine (St. Louis, MO) research group
showing restriction of tumor growth with a novel mRNA therapeutic
delivered in nanoparticles based on the Company’s SemaPhore™
delivery platform.
Expression of the ZBTB46 gene with SemaPhore was
associated with an immunostimulatory tumor microenvironment (TME),
and it was potentiated when combined with anti-PD1 immune
checkpoint inhibition. The manuscript describing the study is
available on a preprint server1 and has been submitted to a
scientific journal for peer-review and potential publication.
The research group, led by Professor Kyunghee
Choi of the Pathology & Immunology Department of Washington
University, was interested in understanding the role that the
ZBTB46 (Zinc Finger and BTB Domain Containing 46) gene plays in the
microenvironment of tumors. The researchers found that
tumor-derived factors frequently downregulate ZBTB46 resulting in a
pro-tumor microenvironment, characterized by dysfunctional
vasculature and immunosuppressive cell accumulation. In contrast,
enforced ZBTB46 expression mitigated the pro-tumor TME features and
restricted tumor growth, suggesting ZBTB46 as a potential target
for tumor treatment.
In a next step, the group tested the systemic
delivery of ZBTB46 mRNA with Altamira’s peptide-based SemaPhore
nanoparticles in mouse models of sarcoma and metastatic breast
cancer to boost ZBTB46 expression. The treatment sustained ZBTB46
expression in tumor-dendritic cells and -endothelial cells and
resulted in the restriction of tumor growth associated with an
immunostimulatory TME.
When combining nanoparticle treatment with an
immune checkpoint inhibitor, the researchers reported that,
“remarkably, the nanoparticles induced dramatic response in both
anti-PD1-responsive […] and -refractory [..] tumor models following
the treatment, generating long-term complete remission of tumor
mass in many of the treated animals challenged with the
anti-PD1-responsive [..] tumor.” They concluded that enforcing
ZBTB46 expression promoted anti-tumor components in the TME, a
prerequisite for effective immune checkpoint blockade therapy, and
could be an effective adjuvant therapy with immunotherapy in cancer
management.
Samuel Wickline, M.D., Altamira’s Chief
Scientific Adviser and a co-author of the manuscript, commented:
“The tumor microenvironment is known to play a key role in cancer
growth. This latest study from the Choi Lab not only identified
ZBTB46 as a key element in the interaction between tumor growth and
tumor microenvironment, but also demonstrated how boosting its
expression by using mRNA can help to attenuate tumor growth. In
addition, it showed very promising synergistic effects with a
well-known immune checkpoint inhibitor. Our SemaPhore nanoparticles
have been designed to reach target diseased cells with systemic
administration and efficiently deliver mRNA therapeutics inside
those cells, and we believe that there is significant potential for
them supporting the development of novel cancer treatment
options.”
About SemaPhore
SemaPhore is a versatile platform designed to
allow for safe and effective delivery of mRNA (messenger
ribonucleic acid) into target cells. It is based on a patented
21-amino acid peptide that can engage any type of RNA in rapid
self-assembly into a polyplex. The polyplex has a size, charge, and
other physical features that allow it to escape hepatic clearance
and thus to reach other target tissues than the liver. SemaPhore
protects the RNA payload from degradation in the circulation and
allows for rapid cellular uptake, while enabling pH-dependent
nucleotide endosomal escape and cytoplasmic delivery. Effective
delivery of mRNA and positive treatment outcomes have been
demonstrated in various murine models of disease, including
osteoarthritis (WNT16), atherosclerosis (p27Kip1) and aortic
aneurysm (SOD2).
About Altamira Therapeutics
Altamira Therapeutics (Nasdaq:CYTO) is dedicated
to developing RNA-based therapeutics for extrahepatic targets
(OligoPhore™ / SemaPhore™ delivery platforms). The Company
currently has two flagship siRNA programs in preclinical
development beyond in vivo proof of concept: AM-401 for KRAS driven
cancer and AM-411 for rheumatoid arthritis. The versatile delivery
platform is also suited for mRNA and other types of RNA
therapeutics and shall be leveraged via out-licensing to pharma or
biotech companies. In addition, Altamira is in the process of
divesting and/or licensing-out its legacy assets in allergology and
viral infection (Bentrio® OTC nasal spray; commercial) and inner
ear therapeutics (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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