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Ex vivo Expansion of Tumor-reactive T Cells by Means of Bryostatin 1/Ionomycin and the Common Gamma Chain Cytokines Formulation
Published on: January 14, 2011
Efficient Artificial T Cell Therapy for Bacterial-Colonized Tumors
Shiyu Zhang1, Han Zhu1, Xintao Peng1
1State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Centre for New Organic Matter, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Centre for Analytical Sciences, College of Chemistry, School of Medicine, and Frontiers Science Centre for Cell Responses, Nankai University, Tianjin, 300071, P. R. China.
Abstract:
Tumor-colonizing bacteria can impede the efficacy of cancer treatments and elevate the risk of metastatic spread. While cytotoxic T lymphocytes (CTLs) are essential for destroying tumor cells, they lack the ability to eliminate bacteria. Here, the artificial T cells (ATC) are presented for tumors, particularly those colonized with intracellular bacteria. The ATC is composed of a hydrogel framework made of disulfide-linked chitosan and hyaluronic acid, encapsulating T cell-derived granzyme B and phage-derived holin. This design leverages the tumor microenvironment for the targeted release of these antitumor and antibacterial agents to precisely kill tumor cells and intracellular bacteria. In vivo studies demonstrate the debris from ATC-mediated destruction acts as an immune stimulator, promoting immune cell infiltration and inhibiting tumor migration. This work highlights the potential of ATC therapy in achieving targeted treatment and robust anti-tumor immunity, advancing the field of artificial cell technologies for precision medicine.

