Peptide antagonists that promote positive selection are inefficient at T cell activation and thymocyte deletion
✍ Scribed by Megan J. Barnden; William R. Heath; Stuart Rodda; Francis R. Carbone
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 521 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
✦ Synopsis
Peptide antagonists that promote positive selection are inefficient at T cell activation and thymocyte deletion*
We set out to determine whether thymocytes from Tcell receptor (TCR) transgenic animals specific for a class I-restricted determinant from ovalbumin (OVA) showed the same fine specificity for antigen-driven deletion in single-cell suspension culture as required for mature T cell activation. The transgenicTCR is specific for the Kb-restricted peptide ovA257-264 (SIINFEKL) which is known to have four TCR contact residues at position 1, 4,6, and 7 from the crystal structure of this fragment in complex with Kb. ovA257-264 analogs systematically substituted at each of these positions were assayed for their ability to promote immature double-positive thymocyte deletion or mature T cell activation of a cytotoxic Tfymphocyte line derived from this transgenic mouse. In the absence of additional antigen-presenting cells, single-cell thymocyte suspensions showed that the specificity for double-positive thymocyte deletion and mature T cell activation was virtually identical, demonstrating a limited cross-reactivtiy with a number of variants having conservative substitutions at these exposed residues. These peptides were considerably more efficient at both thymic deletion and mature T cell activation than a number of non-conservative substitution analogs known to act as antagonists of ovA257-264 and capable of selecting transgenic T cells in thymic organ culture. Therefore, both peripheral T cell activation and thymic deletion have an overall similar pattern of peptide specificity which differs from that required for positive selection. This suggests that a subset of major histocompatibility complex-presented peptides could promote positive selection without causing either thymic deletion or peripheral activation of those selected T cells.