The molecular signature of CD8+ T cells undergoing deletional tolerance

IA Parish, S Rao, GK Smyth, T Juelich… - Blood, The Journal …, 2009 - ashpublications.org
IA Parish, S Rao, GK Smyth, T Juelich, GS Denyer, GM Davey, A Strasser, WR Heath
Blood, The Journal of the American Society of Hematology, 2009ashpublications.org
Peripheral tolerance induction is critical for the maintenance of self-tolerance and can be
mediated by immunoregulatory T cells or by direct induction of T-cell anergy or deletion.
Although the molecular processes underlying anergy have been extensively studied, little is
known about the molecular basis for peripheral T-cell deletion. Here, we determined the
gene expression signature of peripheral CD8+ T cells undergoing deletional tolerance,
relative to those undergoing immunogenic priming or lymphopenia-induced proliferation …
Abstract
Peripheral tolerance induction is critical for the maintenance of self-tolerance and can be mediated by immunoregulatory T cells or by direct induction of T-cell anergy or deletion. Although the molecular processes underlying anergy have been extensively studied, little is known about the molecular basis for peripheral T-cell deletion. Here, we determined the gene expression signature of peripheral CD8+ T cells undergoing deletional tolerance, relative to those undergoing immunogenic priming or lymphopenia-induced proliferation. From these data, we report the first detailed molecular signature of cells undergoing deletion. Consistent with defective cytolysis, these cells exhibited deficiencies in granzyme up-regulation. Furthermore, they showed antigen-driven Bcl-2 down-regulation and early up-regulation of the proapoptotic protein Bim, consistent with the requirement of this BH3-only protein for peripheral T-cell deletion. Bim up-regulation was paralleled by defective interleukin-7 receptor α (IL-7Rα) chain reexpression, suggesting that Bim-dependent death may be triggered by loss of IL-7/IL-7R signaling. Finally, we observed parallels in molecular signatures between deletion and anergy, suggesting that these tolerance pathways may not be as molecularly distinct as previously surmised.
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