共 106 条
T-cell receptor binding affinities and kinetics: impact on T-cell activity and specificity
被引:276
作者:
Stone, Jennifer D.
[1
]
Chervin, Adam S.
[1
]
Kranz, David M.
[1
]
机构:
[1] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
来源:
关键词:
agonists;
antagonists;
binding affinity;
coreceptors;
dissociation rate;
major histocompatibility complex;
peptide specificity;
peptide-major histocompatibility complex;
serial triggering;
T-cell receptor;
T-cell receptor clustering;
MAJOR HISTOCOMPATIBILITY COMPLEX;
MHC CLASS-I;
IMMUNOLOGICAL SYNAPSE;
MULTIVALENT ENGAGEMENT;
CONFORMATIONAL-CHANGES;
LIGAND RECOGNITION;
CROSS-REACTIVITY;
PEPTIDE LIGANDS;
CD8;
CORECEPTOR;
ALPHA-3;
DOMAIN;
D O I:
10.1111/j.1365-2567.2008.03015.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The interaction between the T-cell receptor (TCR) and its peptide-major histocompatibility complex (pepMHC) ligand plays a critical role in determining the activity and specificity of the T cell. The binding properties associated with these interactions have now been studied in many systems, providing a framework for a mechanistic understanding of the initial events that govern T-cell function. There have been various other reviews that have described the structural and biochemical features of TCR : pepMHC interactions. Here we provide an overview of four areas that directly impact our understanding of T-cell function, as viewed from the perspective of the TCR : pepMHC interaction: (1) relationships between T-cell activity and TCR : pepMHC binding parameters, (2) TCR affinity, avidity and clustering, (3) influence of coreceptors on pepMHC binding by TCRs and T-cell activity, and (4) impact of TCR binding affinity on antigenic peptide specificity.
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页码:165 / 176
页数:12
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