Abstract
To better understand the T cell-mediated processes involved in the immune response to herpes simplex virus type 1 (HSV-1) infection, two HSV-specific T cell receptor (TCR) transgenic mouse lines were produced. These mice (gBT-I.1 and gBT-I.3) are MHC class I-restricted and specific for the immunodominant peptide from HSV glycoprotein B (gB), gB498-505. Although derived from the same clone, the mice differ in the chromosomal location of the TCR transgenes and show marked differences in TCR α/β expression on both CD4+ and CD8+ cells in the thymus. Despite this, peripheral CD8+ T cells from both mice express equally high levels of the transgenic TCR and bind the KbgB498-505 tetramer to the same degree. In concordance with this, both were shown to respond equally well in vitro upon stimulation with the gB498-505 peptide or HSV-infected cells. These data show that selection of broadly equivalent peripheral T-cell subsets can occur in the presence of distinctly different thymic T-cell subsets.
| Original language | English |
|---|---|
| Pages (from-to) | 156-163 |
| Number of pages | 8 |
| Journal | Immunology and Cell Biology |
| Volume | 80 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 22 Apr 2002 |
| Externally published | Yes |
Keywords
- CD8 T lymphocyte
- Cytotoxic T lymphocyte
- Herpes simplex virus
- Major histocompatibility complex class I
- T cell receptor
- Thymus
- Transgenic T cell receptor