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Biology subjects

Islam, S. F.

Publications and source records attributed to Islam, S. F..

2 recordsLinked to original sources

Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy

Adoptive T cell therapy (ACT) using chimeric antigen receptor (CAR) engineered T cells is currently being explored in multiple cancer types beyond leukemia/lymphoma. A key step in CAR-T cell manufacturing is the activation and expansion of T cells, which facilitates viral transduction, however, may hamper T cell fitness and reduce in vivo persistence. We developed "T-Expand" for T cell activation and expansion, comprising dextran-based nanoparticles (NPs) conjugated with anti-CD3 and anti-CD28 antibodies. The NPs triggered robust polyclonal expansion of human T cells with efficiency in the range of commercial microbeads (Dynabeads). Engineered in presence of T-Expand, CD19 CAR T cells exhibited enhanced proliferative capacity, cytotoxicity and persistence in vitro, and furthermore, showed superior anti-lymphoma activity in mouse models resulting in complete tumor clearance at one fourth of the CAR T cell dose. Importantly, T-Expand is biocompatible with no observed toxicity, circumventing removal steps after T cell expansion compared to DynabeadsTM. As a biocompatible T cell expansion platform, T-Expand simplifies the manufacturing process while enhancing T cell persistence and functionality, thereby holding promise for increasing clinical efficacy of CAR T cell therapy. O_FIG O_LINKSMALLFIG WIDTH=165 HEIGHT=200 SRC="FIGDIR/small/648181v1_ufig1.gif" ALT="Figure 1"> View larger version (74K): org.highwire.dtl.DTLVardef@35337corg.highwire.dtl.DTLVardef@c75199org.highwire.dtl.DTLVardef@1be184forg.highwire.dtl.DTLVardef@12e1683_HPS_FORMAT_FIGEXP M_FIG Graphical abstract/Cover figureIllustration of CAR T cell manufacturing using T-Expands ex vivo. C_FIG

immunology↗

Regulating Human T Lymphocytes Through Magnetogenetic Tools

The field of synthetic biology has expanded the possibilities for controlling cellular functions, particularly in the development of mammalian cells for therapeutic applications. This study explored the application of magnetogenetic tools to regulate T cell activity, a crucial aspect of developing advanced immunotherapies. Magnetogenetic tools use magnetic fields to remotely control engineered ion channels and protein domains, providing non-invasive, deep-tissue stimulation that overcomes the limitations of traditional methods. We investigated the effects of three magnetogenetic tools - engineered TRPV1 (TRP1-Fer) and TRPV4 (TRP4-Fer) channels, and Electromagnetic Perceptive Gene (EPG) - in Jurkat cells. First, calcium concentration measurements confirmed the activity of these tools within the cells. Using qPCR and proteomics analysis, we then analyzed their impact on T cell activation, calcium signaling, mitochondrial function, membrane integrity, and gene expression under both stimulated (with antigens) and non-stimulated conditions. Our results revealed significant upregulation of activation and calcium-handling proteins in stimulated cells, indicating enhanced activation and cytoskeletal dynamics compared to controls. However, in non-stimulated cells, the magnetogenetic tools unexpectedly led to deactivation of T cells. This investigation showed that while magnetic induction alone deactivated the cells, antigen stimulation in conjunction with magnetic induction amplified cell activation. This study highlights the potential of magnetogenetics to precisely modulate T cell functions, presenting promising avenues for more effective and controlled immunotherapies. However, the findings also underscore the need for careful optimization to mitigate potential adverse effects on cellular integrity and function.

bioengineering↗