SQZ Biotechnologies Presents New AAC, eAPC Platform Research and First Enhanced Tumor Infiltrating Lymphocyte Preclinical Data at Society for Immunotherapy of Cancer Annual Meeting
SQZ Biotechnologies (NYSE: SQZ) showcased promising preclinical research at the 36th Annual Meeting of the Society for Immunotherapy of Cancer, highlighting their SQZ™ AACs and eAPC platforms. These findings suggest a synergistic effect when SQZ™ AACs were combined with cisplatin chemotherapy in HPV16+ cancer models, significantly increasing median survival. Additionally, their engineered tumor infiltrating lymphocytes (TILs) show potential without exogenous IL-2 support, enhancing therapeutic options for various cancer types. This innovative approach could broaden treatment accessibility and efficacy for patients.
- SQZ™ AACs demonstrated synergistic effects with cisplatin chemotherapy, increasing median survival in HPV16+ cancer models.
- SQZ™ eAPCs generated robust CD8+ T cell responses, showing potential for wider application across diverse HPV16+ patient populations.
- Engineered TILs exhibited enhanced potency without the need for external IL-2 support, potentially eliminating toxic preconditioning.
- None.
SQZ™ AACs Demonstrate Synergistic Effects with Chemotherapy in HPV16+ Cancer Model
SQZ™ eAPCs Engineered with Multiple mRNAs Drive Robust CD8+ T Cell Response and are Potentially Applicable to Broader HPV16+ Cancer Patient Population
mRNA Engineered TILs Show Potency without Additional IL-2 Support in Melanoma Model
“Our presentations at SITC provide compelling new preclinical data on the multiple biologically diverse, directed immunity approaches that we are pursuing for cancer therapies,” said
“We are also excited to present initial preclinical results on enhanced tumor infiltrating lymphocytes, highlighting a potential future therapeutic avenue,” said
Major Findings from
Poster #156: RBC-Derived, Activating Antigen Carriers (SQZ™ AACs) Prime Potent T Cell Responses and Drive Tumor Regression In Vivo
- SQZ™ Activating Antigen Carriers (AAC) were derived from red blood cells (RBCs) and engineered to direct tumor-specific antigens and adjuvant to endogenous professional APCs, which subsequently activated T cell responses in vivo
- In TC-1 tumor bearing mice, a model of HPV16+ cancers, AACs demonstrated a synergistic therapeutic effect in combination with cisplatin, a common chemotherapy used in many clinical settings
- Median survival of mice increased in all combination treatment cohorts compared to single agent cisplatin or ACC treatment
Poster #211: SQZ™ eAPCs Generated from PBMCs by Delivery of Multiple mRNAs Encoding for Antigens, Costimulatory Proteins, and Engineered Cytokines
- SQZ™ Enhanced Antigen Presenting Cells (eAPC) derived from peripheral blood mononuclear cells (PBMCs) and engineered with various mRNA encoding for multiple target antigens and immuno-stimulation signals, including CD86 and membrane bound IL-2 and IL-12, generated robust T cell responses in human in-vitro models
- HPV16-encoding mRNA delivery to PBMCs stimulated CD8+ T cells across a range of HLA haplotypes, supporting future eAPC clinical development in broad HPV16+ patient populations
- eAPC data highlights the potential to expand the therapeutic impact across tumor types by changing the antigen-encoding mRNA
Poster #165: Generating Enhanced Tumor Infiltrating Lymphocytes through Microfluidic Cell Squeezing
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Cell Squeeze® delivery of mRNA encoding membrane bound IL-2 (mbIL2) and IL-12 (mbIL12) into expanded tumor reactive CD8 human tumor infiltrating lymphocytes (TILs) from
AgonOx * (AGX-148) demonstrated high levels of membrane-bound cytokine expression in vitro - Enhanced TILs proliferated independent of exogenous IL-2 and demonstrated improved granzyme B levels, illustrating the potential to eliminate systemic IL-2 administration in the clinical setting.
- In an in vitro co-culture model with matched human melanoma cells, enhanced TILs demonstrated increased tumor killing as compared to un-modified TILs
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FAQ
What were the main findings of SQZ Biotechnologies' recent research presented at SITC?
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