Abstract
During an immune response antigen-primed B-cells increase their antigen responsiveness by affinity maturation mediated by somatic hypermutation of the genes encoding the antigen-specific B-cell receptor (BCR) and by selection of higher-affinity B cell clones. Unlike the BCR, the T-cell receptor (TCR) cannot undergo affinity maturation. Nevertheless, antigen-primed T cells significantly increase their antigen responsiveness compared to antigen-inexperienced (nave) T cells in a process called functional avidity maturation. This paper covers studies that describe differences in T-cell antigen responsiveness during T-cell differentiation along with examples of the mechanisms behind functional avidity maturation in T cells.
Originalsprog | Engelsk |
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Artikelnummer | 163453 |
Tidsskrift | Clinical & Developmental Immunology |
Vol/bind | 2012 |
Antal sider | 8 |
ISSN | 1740-2522 |
DOI | |
Status | Udgivet - jan. 2012 |