SQZ Biotechnologies Publishes Preclinical Research Demonstrating SQZ® AAC Platform’s Potential as an Effective Red Blood Cell-Derived Immunotherapy
SQZ Biotechnologies (NYSE: SQZ) has published preclinical research demonstrating the effectiveness of its Activating Antigen Carrier (AAC) platform in activating CD8 T cells and enhancing their tumor infiltration, leading to improved anti-tumor responses. The study, published in Frontiers in Immunology, revealed that combining AAC therapy with Cisplatin, a chemotherapy agent, significantly increased efficacy in a mouse tumor model. The AACs, engineered from red blood cells, are designed to deliver tumor antigens to professional antigen presenting cells, promoting T cell activation.
- Demonstrated potential of AAC technology to activate CD8 T cells effectively.
- Combination of AAC therapy with Cisplatin significantly enhanced treatment efficacy in mouse models.
- AACs resulted in a 12-fold improvement in CD8+ T cell infiltration.
- None.
Activating Antigen Carriers (AACs) Shown Preclinically to Activate CD8 T Cells, Increase Their Tumor Infiltration and Drive Tumor Killing
Demonstrated Improved Efficacy of AAC Therapy Through Combination with Chemotherapy Agent
“This paper demonstrates the potential of our technology to generate an effective red blood cell-derived cancer immunotherapy,” said
The company’s engineered RBCs are designed to transport their cargo of antigen and adjuvant to professional antigen presenting cells (APCs) in the body. The published data demonstrate that when these professional APCs process the engineered RBC, they present the desired antigen to endogenous T cells and drive their activation. This approach to generate RBC therapeutics could be tailored to deliver a variety of antigen and adjuvant materials, and other possible agents, to potentially enhance different aspects of anti-tumor immunity.
“We are excited about the preclinical findings of our AAC program, which has shown potential in both monotherapy settings and in combination with chemotherapy,” said
Study Findings:
- Generation of AACs: Investigators used the Cell Squeeze® technology to engineer RBCs with E6 and E7 antigens and the adjuvant, poly I:C. This process generates AACs that resemble aged RBCs which triggers rapid clearance by professional APCs.
- Effective Delivery to APCs: The method leverages the natural process of RBC clearance to deliver tumor antigens to endogenous professional APCs without the use of chemical or viral vectors.
- Antigen-Specific Activation of T cells: AAC uptake, antigen processing, and presentation by APCs drove antigen-specific activation of T cells in mouse in vivo and human in vitro systems. In a mouse model of HPV16+ tumors, AAC therapy demonstrated significant anti-tumor effects including 12-fold improvement in CD8+ T cell infiltration and 900-fold improvement in E7 antigen-specific CD8+ T cell infiltration compared to untreated animals.
- Enhanced Efficacy with Addition of Cisplatin: The combination of AAC therapy and the chemotherapeutic agent Cisplatin, a common treatment for HPV-driven tumors, increased the efficacy of the treatment in a preclinical tumor model.
About SQZ-AAC-HPV
SQZ® AACs are generated by squeezing red blood cells (RBCs) with antigens and activating adjuvant. The process is tuned to make the engineered RBCs appear aged. Once administered to patients, SQZ® AACs aim to be rapidly taken up by professional antigen presenting cells through a natural process to destroy aged RBCs in the body known as eryptosis. After being taken up, the encapsulated antigen and adjuvant within SQZ® AACs is released, allowing for antigen processing and maturation of professional, endogenous antigen presenting cells in the lymphoid organs, and drives subsequent activation of HPV-specific T cells. SQZ-AAC-HPV is the first product candidate from the SQZ® AAC platform.
About Human Papillomavirus Positive Cancers
Human papillomavirus (HPV) is one of the most common viruses worldwide and certain strains persist for many years, often leading to cancer. According to the
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Investor Contact:
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857-760-0398
Media Contact:
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