Abstract
Recently we reported on a novel H2E transgenic, IA-negative model of experimental autoimmune thyroiditis (EAT) that excludes reactivity to self in its susceptibility pattern to heterologous thyroglobulin (Tg). In conventional, susceptible mouse strains, EAT is inducible with both homologous and heterologous Tg; e.g., human (h)Tg shares conserved thyroiditogenic epitopes with mouse (m)Tg. However, when an H2Eak transgene is introduced into class II-negative B10.Ab0 mice, which express neither surface IA (mutant Aβ-chain) nor surface IE (nonfunctional Ea gene), the resultant H2Eb molecules are permissive for EAT induction by hTg, but not self mTg. Also, the hTg-primed cells do not cross-react with mTg. To explore this unique capacity of E+B10.Ab0 mice to distinguish self from nonself Tg, we have developed T cell lines to examine the T cell receptor repertoire and observed a consistent Vβ8+ component after repeated hTg stimulation. Enrichment and activation of Vβ8+ T cells by either superantigen staphylococcal entertoxin B or anti-Vβ8 in vitro enabled thyroiditis transfer to untreated A-E+ recipients, similar to hTg activation. Vβ8+ T cells isolated by FACS from hTg-immunized mice also proliferated to hTg in vitro. These studies support the contribution of Vβ8 genes to the pathogenicity of hTg in this H2A-E+ transgenic model.
Original language | English |
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Pages (from-to) | 63-70 |
Number of pages | 8 |
Journal | Cellular Immunology |
Volume | 212 |
Issue number | 1 |
DOIs | |
Publication status | Published - 25 Aug 2001 |
Externally published | Yes |
Keywords
- Autoimmune thyroiditis
- Autoimmunity
- EAT
- H2E transgene in EAT
- Human thyroglobulin
- TCRBV usage
- Vβ8 T cells
ASJC Scopus subject areas
- Immunology