Cutting edge: negative selection of immature thymocytes by a few peptide-MHC complexes: differential sensitivity of immature and mature T cells
The Journal of Immunology, 1999•journals.aai.org
We quantitated the number of peptide-class II MHC complexes required to affect the deletion
or activation of 3A9 TCR transgenic thymocytes. Deletion of immature double positive
thymocytes was very sensitive, taking place with approximately three peptide-MHC
complexes per APC. However, the activation of mature CD4+ thymocytes required 100-fold
more complexes per APC. Therefore, a “biochemical margin of safety” exists at the level of
the APC. To be activated, autoreactive T cells in peripheral lymphoid tissues require a …
or activation of 3A9 TCR transgenic thymocytes. Deletion of immature double positive
thymocytes was very sensitive, taking place with approximately three peptide-MHC
complexes per APC. However, the activation of mature CD4+ thymocytes required 100-fold
more complexes per APC. Therefore, a “biochemical margin of safety” exists at the level of
the APC. To be activated, autoreactive T cells in peripheral lymphoid tissues require a …
Abstract
We quantitated the number of peptide-class II MHC complexes required to affect the deletion or activation of 3A9 TCR transgenic thymocytes. Deletion of immature double positive thymocytes was very sensitive, taking place with approximately three peptide-MHC complexes per APC. However, the activation of mature CD4+ thymocytes required 100-fold more complexes per APC. Therefore, a “biochemical margin of safety” exists at the level of the APC. To be activated, autoreactive T cells in peripheral lymphoid tissues require a relatively high level of peptide-MHC complexes.
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