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Biology subjects

Rath, J. A.

Publications and source records attributed to Rath, J. A..

2 recordsLinked to original sources

Designed allosteric biosensors for engineered T cell therapy of cancer

Adoptive cell therapy with chimeric antigen receptor (CAR) T cells has transformed standard-of-care for selected hematologic malignancies, but relapses are frequent and efficacy against solid tumors remains limited1,2. The tumor microenvironment (TME) plays a key role in tumor progression3, and both soluble and cellular TME components can limit CAR-T cell function and persistence4. Targeting soluble TME factors to enhance anti-tumor responses of engineered T cells through chimeric receptors is not yet broadly explored due to the unpredictable signaling characteristics of synthetic protein receptors. Here we developed a protein design platform for the de novo bottom-up assembly of allosteric receptors with programmable input-output behaviors that respond to soluble TME factors with co-stimulation and cytokine signals in T cells, called T-SenSER (TME-sensing switch receptor for enhanced response to tumors). We developed two sets of T-SenSERs targeting vascular endothelial growth factor (VEGF) or colony stimulating factor 1 (CSF1), that are both selectively enriched in a variety of tumors. Combination of CAR and T-SenSER in human T cells enhanced anti-tumor responses in models of lung cancer and multiple myeloma, in a VEGF or CSF1-dependent manner. Our study sets the stage for the accelerated development of synthetic biosensors with custom-built sensing and responses for basic and translational cell engineering applications.

bioengineering↗

Defining the emergence of myeloid-derived suppressor cells in breast cancer using single-cell transcriptomics

Myeloid-derived suppressor cells (MDSCs) are innate immune cells that acquire the capacity to suppress adaptive immune responses during cancer. It remains elusive how MDSCs differ from their normal myeloid counterparts, which limits our ability to specifically detect and therapeutically target MDSCs during cancer. Here, we used single-cell RNAseq to compare MDSC-containing splenic myeloid cells from breast tumor-bearing mice to wildtype controls. Our computational analysis of 14,646 single-cell transcriptomes reveals that MDSCs emerge through a previously unrealized aberrant neutrophil maturation trajectory in the spleen giving rise to a unique chemokine-responsive, immunosuppressive cell state that strongly differs from normal myeloid cells. We establish the first MDSC-specific gene signature and identify novel surface markers for improved detection and enrichment of MDSCs in murine and human samples. Our study provides the first single-cell transcriptional map defining the development of MDSCs, which will ultimately enable us to specifically target these cells in cancer patients.\n\nOne Sentence SummaryWe used single cell transcriptomics to identify the unique molecular features distinguishing myeloid-derived suppressor cells (MDSCs) from their normal, myeloid counterparts, which enabled us to reveal distinct transitory gene expression changes during their maturation in the spleen, and to identify novel cell surface markers for improved detection and isolation of MDSCs.

cancer biology↗