News Release
Synlogic Presents Data from Immuno-Oncology Development Program Demonstrating Potent Anti-Tumor Immunity Following Administration of Novel STING Agonist-producing Synthetic Biotic™ Medicine
- Data presented at Keystone Symposium demonstrate rapid tumor
rejection in preclinical models -
- Data support
advancement of Synthetic Biotic medicines as potential immuno-therapies
for cancer -
“These data provide compelling, early scientific evidence supporting the development of our Synthetic Biotic medicines as potential novel immunotherapeutic agents for the treatment of various cancers,” said J.C. Gutiérrez-Ramos, Ph.D., Synlogic’s president and chief executive officer. “The results demonstrate that we can design Synthetic Biotic medicines that dramatically modulate the tumor microenvironment, by generating potent and efficacious antitumor immunity, turning what is known as a “cold” tumor “hot” and resulting in greatly enhanced response rates. Our Synthetic Biotic medicines can be administered by intratumoral injection enabling achievement of these beneficial effects locally and without systemic toxicity. Moreover, we can engineer additional activities into this new class of living medicines that enhance and sustain the anti-tumor response. In the coming year we intend to advance these IO program candidates into IND-enabling studies.”
The data presented at the meeting demonstrate the antitumor effects of treatment with a probiotic strain of E.coli engineered to produce inducible levels of STING (STimulator of INterferon Genes) agonist (SYN-STING). The STING pathway plays a critical role in the control of tumor growth at both steady state and following a variety of cytolytic and immune-based therapies. SYN-STING can be delivered directly into the tumor enabling its localized site of action in the tumor microenvironment. The approach of using intra-tumoral injection elicits innate responses in the tumor but not in the circulation, decreasing the risk of adverse events that may arise from the production of systemic interferon.
Specifically, the data demonstrated that the production of ci-di-AMP by SYN-STING results in the local upregulation of interferon beta by macrophages and dendritic cells in vitro, andthe rapid rejection of established B16F10 tumors in vivo. Treatment results in an early rise in a variety of potent cytokines, including interferon beta, followed by the activation of effector T cells in the tumor-draining lymph nodes and upregulation of molecules associated with a cytolytic T cell response in the tumor. Taken together, these data demonstrate the ability of Synthetic Biotic medicines to dramatically modulate the tumor microenvironment, generating potent and efficacious antitumor immunity.
About Synthetic Biotic Medicines
Synlogic’s innovative new
class of Synthetic Biotic medicines leverages the tools and principles
of synthetic biology to genetically engineer probiotic microbes to
perform or deliver critical functions missing or damaged due to disease.
The company’s two lead programs target a group of rare metabolic
diseases – inborn errors of metabolism (IEM). Patients with these
diseases are born with a faulty gene, inhibiting the body’s ability to
break down commonly occurring by-products of digestion that then
accumulate to toxic levels and cause serious health consequences. When
delivered orally, these medicines can act from the gut to compensate for
the dysfunctional metabolic pathway and have a systemic effect.
Synthetic Biotic medicines are designed to clear toxic metabolites
associated with specific metabolic diseases and have the potential to
significantly improve symptoms of disease for affected patients.
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Source:
Synlogic
MEDIA CONTACT:
Courtney Heath, 617-872-2462
courtney@scientpr.com
or
INVESTOR
CONTACT:
Elizabeth Wolffe, Ph.D., 617-207-5509
liz@synlogictx.com