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Combining Adhesive Nanostructured Surfaces and Costimulatory Signals to Increase T Cell Activation

https://doi.org/10.1021/acs.nanolett.8b02588

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Orientational Coupling Locally Orchestrates a Cell Migration Pattern for Re‐Epithelialization

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Nanostructured Ordering of Fluorescent Markers and Single Proteins on Substrates

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A Molecular Toolkit for the Functionalization of Titanium‐Based Biomaterials That Selectively Control Integrin‐Mediated Cell Adhesion

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Regulation of delta opioid receptor expression by anti-CD3-ε, PMA, and ionomycin in murine splenocytes and T cells

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Multiple targets for brefeldin A

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Abnormal T-cell phenotype in familial erythrophagocytic lymphohistiocytosis

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Role of the CD28 receptor in T-cell activation

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Alteration of intracellular traffic by monensin; mechanism, specificity and relationship to toxicity

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Activation of human T lymphocytes via integrin signaling induced by RGD-disintegrins

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Cell Surface Molecules and Early Events Involved in Human T Lymphocyte Activation

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Synthesis of Binary Nanopatterns on Hydrogels for Initiating Cellular Responses

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Integrin-Assisted T-Cell Activation on Nanostructured Hydrogels

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Nanomechanical Force Mapping of Restricted Cell-To-Cell Collisions Oscillating between Contraction and Relaxation

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Combinatorial Nano–Bio Interfaces

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Artificial 3D Culture Systems for T Cell Expansion

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Structural and Functional Aspects of RGD-Containing Cyclic Pentapeptides as Highly Potent and Selective Integrin αVβ3Antagonists

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Ordered Deposition of Inorganic Clusters from Micellar Block Copolymer Films

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Fine Tuning and Efficient T Cell Activation with Stimulatory aCD3 Nanoarrays

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

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T Cell Activation is Determined by the Number of Presented Antigens

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Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule

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CD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs

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Complete but curtailed T-cell response to very low-affinity antigen

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Progressive differentiation and selection of the fittest in the immune response

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A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins

inferredcites →https://doi.org/10.1056/nejmoa1103849openalex-snapshot

Chimeric Antigen Receptor–Modified T Cells in Chronic Lymphoid Leukemia

inferredcites →https://doi.org/10.1083/jcb.116.5.1071openalex-snapshot

Brefeldin A: insights into the control of membrane traffic and organelle structure.

inferredcites →https://doi.org/10.1084/jem.173.3.759openalex-snapshot

The CD28 ligand B7/BB1 provides costimulatory signal for alloactivation of CD4+ T cells.

inferredcites →https://doi.org/10.1111/imr.12129openalex-snapshot

Human cell‐based artificial antigen‐presenting cells for cancer immunotherapy

inferredcites →https://doi.org/10.1111/imr.12135openalex-snapshot

Uncoupling T‐cell expansion from effector differentiation in cell‐based immunotherapy

inferredcites →https://doi.org/10.1111/j.1365-3083.1991.tb01787.xopenalex-snapshot

Mechanism of Calcium Ionophore and Phorbol Ester‐Induced T‐cell Activation

inferredcites →https://doi.org/10.1111/j.1432-1033.1990.tb15478.xopenalex-snapshot

Protein kinase C and T cell activation

inferredcites →https://doi.org/10.1116/1.3536839openalex-snapshot

Nanopatterning by block copolymer micelle nanolithography and bioinspired applications

inferredcites →https://doi.org/10.1126/science.1260044openalex-snapshot

Antigen affinity, costimulation, and cytokine inputs sum linearly to amplify T cell expansion

inferredcites →https://doi.org/10.1126/scitranslmed.3002842openalex-snapshot

T Cells with Chimeric Antigen Receptors Have Potent Antitumor Effects and Can Establish Memory in Patients with Advanced Leukemia

inferredcites →https://doi.org/10.1126/scitranslmed.aac5415openalex-snapshot

Chimeric antigen receptor T cells persist and induce sustained remissions in relapsed refractory chronic lymphocytic leukemia

inferredcites →https://doi.org/10.1146/annurev-immunol-030409-101212openalex-snapshot

Differentiation of Effector CD4 T Cell Populations

inferredcites →https://doi.org/10.1182/blood-2010-05-286286openalex-snapshot

Human effector CD8+ T cells derived from naive rather than memory subsets possess superior traits for adoptive immunotherapy

inferredcites →https://doi.org/10.1529/biophysj.106.089730openalex-snapshot

Cell Spreading and Focal Adhesion Dynamics Are Regulated by Spacing of Integrin Ligands

inferredcites →https://doi.org/10.3389/fimmu.2016.00006openalex-snapshot

TCR Signal Strength Alters T–DC Activation and Interaction Times and Directs the Outcome of Differentiation

inferredcites →https://doi.org/10.4049/jimmunol.143.4.1283openalex-snapshot

Mechanisms of T cell activation by the calcium ionophore ionomycin.

inferredcites →https://doi.org/10.4049/jimmunol.145.3.785openalex-snapshot

Fibronectin promotes proliferation of naive and memory T cells by signaling through both the VLA-4 and VLA-5 integrin molecules.

inferredcites →https://doi.org/10.4049/jimmunol.159.12.5921openalex-snapshot

Effects of CD28 costimulation on long-term proliferation of CD4+ T cells in the absence of exogenous feeder cells

inferredcites →https://doi.org/10.4049/jimmunol.162.6.3256openalex-snapshot

Inflammatory Cytokines Provide a Third Signal for Activation of Naive CD4+ and CD8+ T Cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Lymph-Node Inspired Hydrogels Enhance CAR Expression and Proliferation of CAR T Cells

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