Abstract |
In a previous study we demonstrated that the human thyroglobulin (hTg) peptide p2340 (aa 2340-2359) can stimulate a T cell response and elicit experimental autoimmune thyroiditis (EAT) in AKR/J (H-2(k)) mice. In the present study we examined whether p2340 can induce EAT in single HLA class II DR3 transgenic mice. This peptide was found to be immunogenic at the T cell level in DR3 mice, since it induced specific proliferative responses, as well as IL-2 and IFN-gamma secretion in secondary cultures of peptide-primed lymph node cells (LNC). Immunization of HLA-DR3 mice with p2340 in CFA elicited EAT (infiltration index of 1 to 2) in eight of nine mice. Peptide-primed LNC responded to intact hTg, whereas, hTg-primed LNC did not respond to p2340 in culture, suggesting that p2340 contains subdominant T cell epitope(s). P2340 was also found to be immunogenic at the B cell level, since strong p2340-specific IgG response was detected in all transgenic mice tested. Thus, we provide evidence for a pathogenic role of an hTg peptide in HLA-DR3 transgenic mice. Therefore, p2340 could be presented by DR3 molecule in patients with Hashimoto's thyroiditis and participate in the development of the disease.
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Authors | Evangelos Karras, Huan Yang, Peggy Lymberi, Premkumar Christadoss |
Journal | Journal of autoimmunity
(J Autoimmun)
Vol. 24
Issue 4
Pg. 291-6
(Jun 2005)
ISSN: 0896-8411 [Print] England |
PMID | 15927791
(Publication Type: Journal Article)
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Chemical References |
- Autoantibodies
- Epitopes, T-Lymphocyte
- HLA-DR3 Antigen
- Immunoglobulin G
- Peptides
- Thyroglobulin
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Topics |
- Animals
- Autoantibodies
(immunology)
- B-Lymphocytes
(immunology, pathology)
- Cells, Cultured
- Epitopes, T-Lymphocyte
(immunology)
- HLA-DR3 Antigen
(genetics, immunology)
- Humans
- Immunoglobulin G
(immunology)
- Mice
- Mice, Transgenic
- Peptides
(administration & dosage, immunology)
- T-Lymphocytes
(immunology, pathology)
- Thyroglobulin
(administration & dosage, immunology)
- Thyroid Gland
(immunology, pathology)
- Thyroiditis, Autoimmune
(chemically induced, immunology, pathology)
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