Polyspecificity of T cell and B cell receptor recognition. - Wikidata - awgldk - TriplyDB

Polyspecificity of T cell and B cell receptor recognition.

Polyspecificity of T cell and B cell receptor recognition.

http://www.wikidata.org/entity/Q36082439

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Network, degeneracy and bow tie. Integrating paradigms and architectures to grasp the complexity of the immune system The Unspecific Side of Acquired Immunity Against Infectious Disease: Causes and Consequences Systemic Lupus Erythematosus: Molecular Mimicry between Anti-dsDNA CDR3 Idiotype, Microbial and Self Peptides-As Antigens for Th Cells Amino Acid Similarity Accounts for T Cell Cross-Reactivity and for “Holes” in the T Cell Repertoire Structure of Epstein-Barr Virus Glycoprotein 42 Suggests a Mechanism for Triggering Receptor-Activated Virus Entry Structural Basis of Specificity and Cross-Reactivity in T Cell Receptors Specific for Cytochrome c-I-E T-cell Receptor Specificity Maintained by Altered Thermodynamics Autoreactivity and Exceptional CDR Plasticity (but Not Unusual Polyspecificity) Hinder Elicitation of the Anti-HIV Antibody 4E10 Deconstructing the Peptide-MHC Specificity of T Cell Recognition Structure-Based Reverse Vaccinology Failed in the Case of HIV Because it Disregarded Accepted Immunological Theory Reconciling views on T cell receptor germline bias for MHC Vasostatin-1 antigenic epitope mapping for induction of cellular and humoral immune responses to chromogranin A autoantigen in NOD mice The molecular basis of TCR germline bias for MHC is surprisingly simple Cysteine-free proteins in the immunobiology of arthropod-borne diseases.Autoimmunity, end organ damage, and the origin of autoantibodies and autoreactive T cells in systemic lupus erythematosus.HLA-DR3 restricted T cell epitope mimicry in induction of autoimmune response to lupus-associated antigen SmD Pathogenesis of systemic lupus erythematosus revisited 2011: end organ resistance to damage, autoantibody initiation and diversification, and HLA-DR.Pathogenesis of kidney disease in systemic lupus erythematosus.Tracing functional antigen-specific CCR6 Th17 cells after vaccination.Novel approaches for identifying target antigens of autoreactive human B and T cells Myelin recovery in multiple sclerosis: the challenge of remyelination Peptide-MHC heterodimers show that thymic positive selection requires a more restricted set of self-peptides than negative selection.An in depth analysis of the concept of "polyspecificity" assumed to characterize TCR/BCR recognition Heterologous immunity between viruses Two mechanisms that account for major histocompatibility complex restriction of T cells.Unbiased identification of target antigens of CD8+ T cells with combinatorial libraries coding for short peptides.Requirements for empirical immunogenicity trials, rather than structure-based design, for developing an effective HIV vaccine.Epitope reactions can be gauged by relative antibody discriminating specificity (RADS) values supported by deletion, substitution and cysteine bridge formation analyses: potential uses in pathogenesis studies.Antigen receptor allelic exclusion: an update and reappraisal Early relaxation dynamics in the LC 13 T cell receptor in reaction to 172 altered peptide ligands: a molecular dynamics simulation study T cell receptor recognition of self and foreign antigens in the induction of autoimmunity.On the logic of restrictive recognition of peptide by the T-cell antigen receptor.Intramolecular polyspecificity in CD4 T-cell recognition of Ad-restricted epitopes of proteoglycan aggrecan.Antigen microarrays identify CNS-produced autoantibodies in RRMS.Cumulative autoimmunity: T cell clones recognizing several self-epitopes exhibit enhanced pathogenicity Implications of Lymphocyte Anergy to Glycolipids in Multiple Sclerosis (MS): iNKT Cells May Mediate the MS Infectious Trigger.Structural insights into activation of antiviral NK cell responses Viral antigen density and confinement time regulate the reactivity pattern of CD4 T-cell responses to vaccinia virus infection.Methods for quantifying T cell receptor binding affinities and thermodynamics.Functional development of the T cell receptor for antigen

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P2860

Polyspecificity of T cell and B cell receptor recognition.

http://www.wikidata.org/entity/Q36082439

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2007 nî lūn-bûn

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Polyspecificity of T cell and B cell receptor recognition.

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Polyspecificity of T cell and B cell receptor recognition.

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Polyspecificity of T cell and B cell receptor recognition.

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Polyspecificity of T cell and B cell receptor recognition.

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Polyspecificity of T cell and B cell receptor recognition.

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Polyspecificity of T cell and B cell receptor recognition.

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J.SMIM.2007.02.012

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Seminars in Immunology

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Polyspecificity of T cell and B cell receptor recognition.

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Byron Goldstein

http://www.w3.org/2001/XMLSchema#string

Clemencia Pinilla

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David C Krakauer

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David Nemazee

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Eli E Sercarz

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Erik S Huseby

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Franco Celada

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Irun R Cohen

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K Christopher Garcia

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Kai W Wucherpfennig

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P2860

Structural and functional consequences of altering a peptide MHC anchor residue

Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide

An alphabeta T cell receptor structure at 2.5 A and its orientation in the TCR-MHC complex

Structure of the complex between human T-cell receptor, viral peptide and HLA-A2

Crystallographic analysis of anti-p24 (HIV-1) monoclonal antibody cross-reactivity and polyspecificity

Structural basis of plasticity in T cell receptor recognition of a self peptide-MHC antigen

Exploring immunological specificity using synthetic peptide combinatorial libraries.

Identification of candidate T-cell epitopes and molecular mimics in chronic Lyme disease.

Structure of an autoimmune T cell receptor complexed with class II peptide-MHC: insights into MHC bias and antigen specificity.

A powerful combination: the use of positional scanning libraries and biometrical analysis to identify cross-reactive T cell epitopes.

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216-224

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scholarly article

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10.1016/J.SMIM.2007.02.012

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4

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19

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David A. Hafler

Alan S. Perelson

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2007-03-29T00:00:00Z

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51381288

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17398114

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2034306

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