Publications by authors named "B DiAndreth"

Logic-gated engineered cells are an emerging therapeutic modality that can take advantage of molecular profiles to focus medical interventions on specific tissues in the body. However, the increased complexity of these engineered systems may pose a challenge for prediction and optimization of their behavior. Here we describe the design and testing of a flow cytometry-based screening system to rapidly select functional inhibitory receptors from a pooled library of candidate constructs.

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Clinical applications of CAR-T cells are limited by the scarcity of tumor-specific targets and are often afflicted with the same on-target/off-tumor toxicities that plague other cancer treatments. A new promising strategy to enforce tumor selectivity is the use of logic-gated, two-receptor systems. One well-described application is termed Tmod™, which originally utilized a blocking inhibitory receptor directed towards HLA-I target antigens to create a protective NOT gate.

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Regulated transgene expression is an integral component of gene therapies, cell therapies and biomanufacturing. However, transcription factor-based regulation, upon which most applications are based, suffers from complications such as epigenetic silencing that limit expression longevity and reliability. Constitutive transgene transcription paired with post-transcriptional gene regulation could combat silencing, but few such RNA- or protein-level platforms exist.

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Immune cells that are engineered with receptors to integrate signals from multiple antigens offer a promising route to achieve the elusive property of therapeutic selectivity in cancer patients. Several types of multi-signal integrators have been described, among them mechanisms that pair activating and inhibitory receptors which are termed NOT gates by analogy to logical operations performed by machines. Here we review one such NOT-gated signal integrator called the Tmod system which is being developed for patients with solid tumors.

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Article Synopsis
  • Progress in treating solid tumors has been limited by the absence of unique targets; however, a new T cell therapy called Tmod™ addresses this challenge by utilizing a dual-receptor system.
  • The Tmod system leverages a genetic difference known as loss of heterozygosity (LOH) to distinguish between tumor and normal cells, using both a chimeric antigen receptor (CAR) or T cell receptor (TCR) for activation and a modified inhibitory receptor to enhance selectivity.
  • This study investigates a blocker targeting the HLA-A*02 antigen alongside two different T-mod constructs and reveals that Tmod functions through mechanisms that reduce receptor sensitivity and activation strength, making it more robust to changes in antigen expression on target cells.
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