Studies of repertoires of mouse monoclonal CD4(+) T cells have revealed several mechanisms of self-tolerance; however, which mechanisms operate in normal repertoires is unclear. Here we studied polyclonal CD4(+) T cells specific for green fluorescent protein expressed in various organs, which allowed us to determine the effects of specific expression patterns on the same epitope-specific T cells. Peptides presented uniformly by thymic antigen-presenting cells were tolerated by clonal deletion, whereas peptides excluded from the thymus were ignored. Peptides with limited thymic expression induced partial clonal deletion and impaired effector T cell potential but enhanced regulatory T cell potential. These mechanisms were also active for T ce...
Conventional and regulatory T cells develop in the thymus where they are exposed to samples of self-...
The specificity with which CD4+ T cells recognize PR8 S1, the major I-E$\rm\sp{d}$-restricted T cell...
AbstractPeripheral T cell maintenance requires a survival signal delivered upon T cell receptor (TCR...
Studies of repertoires of mouse monoclonal CD4(+) T cells have revealed several mechanisms of self-t...
To examine mechanisms by which CD4+ T cell tolerance is established to self-peptides, we analyzed se...
A clear understanding of the formation of the CD4+CD25+ regulatory T cell repertoire in the thymus a...
Previous experiments showed that peptides corresponding to a major CD4-binding site on the β2 domain...
To better understand immune tolerance to class-II restricted antigens, we investigated T cell tolera...
AbstractThe influence of individual peptides in thymic selection was examined in H2-M− mice, in whic...
AbstractThe role of self-peptides in positive selection of CD4+ T cells has been controversial. We s...
AbstractTo understand how thymic selection gives rise to T cells that are capable of major histocomp...
Deletion of self-antigen-specific T cells during thymic development provides protection from autoimm...
The specificity with which CD4+ T cells recognize self peptides in vivo was examined in transgenic m...
The immune system is charged with the daunting task of discriminating self-antigens from an endless ...
In both humans and mice, CD4+ T cells reactive to self-derived antigens have been implicated in a ra...
Conventional and regulatory T cells develop in the thymus where they are exposed to samples of self-...
The specificity with which CD4+ T cells recognize PR8 S1, the major I-E$\rm\sp{d}$-restricted T cell...
AbstractPeripheral T cell maintenance requires a survival signal delivered upon T cell receptor (TCR...
Studies of repertoires of mouse monoclonal CD4(+) T cells have revealed several mechanisms of self-t...
To examine mechanisms by which CD4+ T cell tolerance is established to self-peptides, we analyzed se...
A clear understanding of the formation of the CD4+CD25+ regulatory T cell repertoire in the thymus a...
Previous experiments showed that peptides corresponding to a major CD4-binding site on the β2 domain...
To better understand immune tolerance to class-II restricted antigens, we investigated T cell tolera...
AbstractThe influence of individual peptides in thymic selection was examined in H2-M− mice, in whic...
AbstractThe role of self-peptides in positive selection of CD4+ T cells has been controversial. We s...
AbstractTo understand how thymic selection gives rise to T cells that are capable of major histocomp...
Deletion of self-antigen-specific T cells during thymic development provides protection from autoimm...
The specificity with which CD4+ T cells recognize self peptides in vivo was examined in transgenic m...
The immune system is charged with the daunting task of discriminating self-antigens from an endless ...
In both humans and mice, CD4+ T cells reactive to self-derived antigens have been implicated in a ra...
Conventional and regulatory T cells develop in the thymus where they are exposed to samples of self-...
The specificity with which CD4+ T cells recognize PR8 S1, the major I-E$\rm\sp{d}$-restricted T cell...
AbstractPeripheral T cell maintenance requires a survival signal delivered upon T cell receptor (TCR...