A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
about
Selection of functional T cell receptor mutants from a yeast surface-display libraryThe Tritope Model for restrictive recognition of antigen by T-cells II. Implications for ontogeny, evolution and physiologyDefinition of agonists and design of antagonists for alloreactive T cell clones using synthetic peptide libraries.Virus-induced abrogation of transplantation tolerance induced by donor-specific transfusion and anti-CD154 antibody.Molecular interactions between extracellular components of the T-cell receptor signaling complex.Heterologous immunity between virusesThymic selection stifles TCR reactivity with the main chain structure of MHC and forces interactions with the peptide side chains.On the logic of restrictive recognition of peptide by the T-cell antigen receptor.H2-DMalpha(-/-) mice show the importance of major histocompatibility complex-bound peptide in cardiac allograft rejectionNegative selection imparts peptide specificity to the mature T cell repertoire.Role of 2CT cell receptor residues in the binding of self- and allo-major histocompatibility complexesA kinetic threshold between negative and positive selection based on the longevity of the T cell receptor-ligand complex.Memory of mice and men: CD8+ T-cell cross-reactivity and heterologous immunity.Mechanism of cellular rejection in transplantationCross-immune tolerance: conception and its potential significance on transplantation tolerancePathogens and immunologic memory in asthma: what have we learned?Activation of a T cell hybridoma by an alloligand results in differential effects on IL-2 secretion and activation-induced cell death.The role of peptides in T cell alloreactivity is determined by self-major histocompatibility complex molecules.Alloreactive T cells respond specifically to multiple distinct peptide-MHC complexes.A similarity in peptide cross-reactivity between alloantigen- and nominal antigen-induced CD8+ T cell responses in vitro.Degeneracy and additional alloreactivity of drug-specific human alpha beta(+) T cell clones.Immunological challenges associated with artificial skin grafts: available solutions and stem cells in future design of synthetic skin.
P2860
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P2860
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
description
1998 nî lūn-bûn
@nan
1998 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@ast
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@en
type
label
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@ast
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@en
prefLabel
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@ast
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@en
P2093
P1433
P1476
A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR.
@en
P2093
P304
P356
10.1016/S1074-7613(00)80559-2
P407
P577
1998-05-01T00:00:00Z