Spatial Regulation of T-Cell Signaling by Programmed Death-Ligand 1 on Wireframe DNA Origami Flat Sheets

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A dynamic CD2-rich compartment at the outer edge of the immunological synapse boosts and integrates signals

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Quantitative Interactomics in Primary T Cells Provides a Rationale for Concomitant PD-1 and BTLA Coinhibitor Blockade in Cancer Immunotherapy

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Antigen-Presenting Cell-Intrinsic PD-1 Neutralizes PD-L1 in cis to Attenuate PD-1 Signaling in T Cells

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T cell costimulatory receptor CD28 is a primary target for PD-1–mediated inhibition

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Magnetic Field-Induced T Cell Receptor Clustering by Nanoparticles Enhances T Cell Activation and Stimulates Antitumor Activity

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Spatial control of membrane receptor function using ligand nanocalipers

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A carbon nanotube–polymer composite for T-cell therapy

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CD28 and CD3 have complementary roles in T-cell traction forces

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Nanoscale Ligand Spacing Influences Receptor Triggering in T Cells and NK Cells

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Programmed cell death 1 forms negative costimulatory microclusters that directly inhibit T cell receptor signaling by recruiting phosphatase SHP2

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Selective Effects of PD-1 on Akt and Ras Pathways Regulate Molecular Components of the Cell Cycle and Inhibit T Cell Proliferation

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TCR and Lat are expressed on separate protein islands on T cell membranes and concatenate during activation

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Self-assembled DNA nanostructures for distance-dependent multivalent ligand–protein binding

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