Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
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Mechanisms behind functional avidity maturation in T cellsQuantitative challenges in understanding ligand discrimination by alphabeta T cellsAntigen-engaged B cells undergo chemotaxis toward the T zone and form motile conjugates with helper T cells.The quantal theory of how the immune system discriminates between "self and non-self"MHC class II association with lipid rafts on the antigen presenting cell surfaceAntigen-Specific T-Cell Activation Independently of the MHC: Chimeric Antigen Receptor-Redirected T CellsModest Interference with Actin Dynamics in Primary T Cell Activation by Antigen Presenting Cells Preferentially Affects Lamellal SignalingT cell receptor-proximal signals are sustained in peripheral microclusters and terminated in the central supramolecular activation cluster.The contributions of mass spectrometry to understanding of immune recognition by T lymphocytes.Quantifying signaling-induced reorientation of T cell receptors during immunological synapse formation.Low T cell receptor expression and thermal fluctuations contribute to formation of dynamic multifocal synapses in thymocytes.CD80 cytoplasmic domain controls localization of CD28, CTLA-4, and protein kinase Ctheta in the immunological synapseStepwise cytoskeletal polarization as a series of checkpoints in innate but not adaptive cytolytic killing.MHC class II deprivation impairs CD4 T cell motility and responsiveness to antigen-bearing dendritic cells in vivo.Spatiotemporal patterning during T cell activation is highly diverse.Spatiotemporal regulation of T cell costimulation by TCR-CD28 microclusters and protein kinase C theta translocation.Specific patterns of Cdc42 activity are related to distinct elements of T cell polarizationA large T cell invagination with CD2 enrichment resets receptor engagement in the immunological synapse.T cell receptor (TCR) clustering in the immunological synapse integrates TCR and costimulatory signaling in selected T cells.A role for rebinding in rapid and reliable T cell responses to antigenClass II MHC self-antigen presentation in human B and T lymphocytesUpregulation of the CLIP self peptide on mature dendritic cells antagonizes T helper type 1 polarization.Differential role of ICAM ligands in determination of human memory T cell differentiationNSOM/QD-based direct visualization of CD3-induced and CD28-enhanced nanospatial coclustering of TCR and coreceptor in nanodomains in T cell activation.Epigenetics in human autoimmunity. Epigenetics in autoimmunity - DNA methylation in systemic lupus erythematosus and beyond.The mature activating natural killer cell immunologic synapse is formed in distinct stages.Epitope density influences CD8+ memory T cell differentiation.A cycle of Zap70 kinase activation and release from the TCR amplifies and disperses antigenic stimuli.Peptide-MHC heterodimers show that thymic positive selection requires a more restricted set of self-peptides than negative selection.CD28 plays a critical role in the segregation of PKC theta within the immunologic synapse.Genomic expression programs and the integration of the CD28 costimulatory signal in T cell activation.p85beta phosphoinositide 3-kinase regulates CD28 coreceptor functionEquilibrium thermodynamics of cell-cell adhesion mediated by multiple ligand-receptor pairs.Real-time analysis of T cell receptors in naive cells in vitro and in vivo reveals flexibility in synapse and signaling dynamics.Presentation of antagonist peptides to naive CD4+ T cells abrogates spatial reorganization of class II MHC peptide complexes on the surface of dendritic cells.How and why does the immunological synapse form? Physical chemistry meets cell biology.Stable T cell-dendritic cell interactions precede the development of both tolerance and immunity in vivo.Tuning immune responses: diversity and adaptation of the immunological synapse.T cell-dendritic cell immunological synapses contain TCR-dependent CD28-CD80 clusters that recruit protein kinase C theta.Opposite effects of endogenous peptide-MHC class I on T cell activity in the presence and absence of CD8.
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Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
description
im Dezember 2001 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2001
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name
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@en
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@nl
type
label
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@en
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@nl
prefLabel
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@en
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@nl
P2093
P356
P1433
P1476
Erratum: Costimulation and endogenous MHC ligands contribute to T cell recognition
@en
P2093
Cenk Sumen
Christoph Wülfing
Lawren C. Wu
Mark M. Davis
Michael D. Sjaastad
P356
10.1038/NI741
P407
P577
2001-12-03T00:00:00Z