SQZ Biotechnologies Announces Publication of Comprehensive Preclinical Research on SQZ® APC’s Ability to Overcome Fundamental Biological Barrier to Effective and Efficient Killer T Cell Activation
SQZ Biotechnologies has published significant preclinical research regarding their Cell Squeeze® platform, demonstrating its capacity to engineer immune cells (T cells, B cells, NK cells, and monocytes) for enhanced MHC-I antigen presentation, crucial for activating killer T cells in disease treatment. This research is published in the Journal of Immunology and supports the development of clinical programs. The platform aims to advance cancer vaccines and improve patient outcomes, with FDA IND clearance for enhanced APCs.
- FDA IND clearance received for enhanced antigen presenting cells (APCs) to commence clinical trials.
- Demonstrated ability to activate a broad range of immune cells, potentially enhancing therapeutic designs.
- Preclinical results show successful activation of endogenous immune responses across multiple antigens.
- The company has incurred significant losses since inception, raising concerns about financial sustainability.
- Potential delays in clinical trials due to regulatory approvals and ongoing uncertainties.
Multiple Immune Cell Types – T cells, B cells, NK cells, and Monocytes – Demonstrate Engineering of MHC-I Antigen Presentation
Paper on the Company’s Cell Squeeze® Platform’s Cell Engineering Capabilities Published in the
The journal publication follows the
“We are excited to publish the comprehensive dataset that has long underpinned our conviction in the SQZ APC platform’s potential for patient impact,” said
CD8, or Killer, T cells play a critical role in combating diseases, however, a major bottleneck for CD8 T cell activation is displaying the desired disease associated antigen(s) to these T cells through the MHC-I pathway. In this journal article, SQZ scientists and their collaborators describe how they overcome this fundamental biological problem through the delivery of antigens directly into the cytosol of immune cells by microfluidic squeezing.
“What’s exciting about our platform is the ability to efficiently insert many types of antigen cargo directly into a cell’s cytosol for presentation to killer T cells, and the ability to engineer other immune system cells to target disease,” said
Major Journal Study Findings
Enabling Cancer Vaccine Development
- In this study, the authors demonstrate preclinically that cytosolic delivery of antigens through microfluidic squeezing enables direct MHC-I antigen presentation to CD8 T cells by diverse immune system cell types, overcoming a major challenge in the development of cancer vaccine therapeutics
- Study authors also showed they could expand beyond the more commonly used dendritic cells to induce T cell activation. MHC-I presentation was demonstrated in engineered T cells, B cells, Natural Killer cells, and monocytes – broadening their potential use and impact in therapeutic design
Tumor Protection and Immunization
- In vivo study findings showed that engineered B cells, T cells, or mixed peripheral blood mononuclear cells (PBMCs), were all capable of activating endogenous immune responses across multiple antigens
- These immune responses were able to protect mice in prophylactic studies, drive tumor regression in therapeutic studies, and form long-term memory that protects against future tumor challenge
- Authors further found that this protection correlates with tumor infiltration of antigen-specific cells with nearly 90 percent of infiltrating CD8 T cells being specific for the tumor antigen delivered using the Cell Squeeze® technology
Efficient, Scaled Manufacturing
- Study authors compared the viability and delivery of engineered cells using research-scale and manufacturing-scale Cell Squeeze® chips. They found that delivery of different cells types within PBMCs was similar across research-scale and manufacturing-scale chips, and study authors demonstrated successful increase from millions to billions of cells processed using manufacturing-scale chips
About
Forward Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation statements relating to our platform development, our product candidates, preclinical and clinical activities, progress and outcomes, development plans, clinical translation, manufacturing, clinical safety and efficacy results, therapeutic impact and market opportunities. These forward-looking statements are based on management's current expectations. Actual results could differ from those projected in any forward-looking statements due to several risk factors. Such factors include, among others, risks and uncertainties related to our limited operating history; our significant losses incurred since inception and expectation to incur significant additional losses for the foreseeable future; the development of our initial product candidates, upon which our business is highly dependent; the impact of the COVID-19 pandemic on our operations and clinical activities; our need for additional funding and our cash runway; the lengthy, expensive, and uncertain process of clinical drug development, including uncertain outcomes of clinical trials and potential delays in regulatory approval; our ability to maintain our relationships with our third party vendors and strategic collaborators; and protection of our proprietary technology, intellectual property portfolio and the confidentiality of our trade secrets. These and other important factors discussed under the caption "Risk Factors" in our Annual Report on Form 10-K, as updated by our Quarterly Report on Form 10-Q for the quarterly period ended
Certain information contained in this press release relates to or is based on studies, publications, surveys and other data obtained from third-party sources and our own internal estimates and research. While we believe these third-party sources to be reliable as of the date of this press release, we have not independently verified, and we make no representation as to the adequacy, fairness, accuracy, or completeness of any information obtained from third-party sources.
View source version on businesswire.com: https://www.businesswire.com/news/home/20220201005355/en/
SQZ Biotechnologies IR:
investors@sqzbiotech.com
SQZ Biotechnologies Media:
Corporate Communications
john.lacey@sqzbiotech.com
781-392-5514
Source:
FAQ
What does SQZ Biotechnologies' recent publication highlight?
What is the significance of the FDA IND clearance for SQZ?
How do the findings impact the potential of cancer therapies?